Top Five Stories of the Cellular Landscape and Therapies of Atherosclerosis: Current Knowledge and Future Perspectives

Qi Pan, Cheng Chen, Yue-jin Yang

Current Medical Science ›› 2023, Vol. 44 ›› Issue (1) : 1-27.

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Current Medical Science ›› 2023, Vol. 44 ›› Issue (1) : 1-27. DOI: 10.1007/s11596-023-2818-2
Review Article

Top Five Stories of the Cellular Landscape and Therapies of Atherosclerosis: Current Knowledge and Future Perspectives

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Abstract

Atherosclerosis (AS) is characterized by impairment and apoptosis of endothelial cells, continuous systemic and focal inflammation and dysfunction of vascular smooth muscle cells, which is documented as the traditional cellular paradigm. However, the mechanisms appear much more complicated than we thought since a bulk of studies on efferocytosis, transdifferentiation and novel cell death forms such as ferroptosis, pyroptosis, and extracellular trap were reported. Discovery of novel pathological cellular landscapes provides a large number of therapeutic targets. On the other side, the unsatisfactory therapeutic effects of current treatment with lipid-lowering drugs as the cornerstone also restricts the efforts to reduce global AS burden. Stem cell- or nanoparticle-based strategies spurred a lot of attention due to the attractive therapeutic effects and minimized adverse effects. Given the complexity of pathological changes of AS, attempts to develop an almighty medicine based on single mechanisms could be theoretically challenging. In this review, the top stories in the cellular landscapes during the initiation and progression of AS and the therapies were summarized in an integrated perspective to facilitate efforts to develop a multi-targets strategy and fill the gap between mechanism research and clinical translation. The future challenges and improvements were also discussed.

Keywords

atherosclerosis / transdifferentiation / extracellular traps / efferocytosis / stem cell / nanoparticles

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Qi Pan, Cheng Chen, Yue-jin Yang. Top Five Stories of the Cellular Landscape and Therapies of Atherosclerosis: Current Knowledge and Future Perspectives. Current Medical Science, 2023, 44(1): 1‒27 https://doi.org/10.1007/s11596-023-2818-2

References

[1]
LibbyP, RidkerPM, HanssonGK. Progress and challenges in translating the biology of atherosclerosis. Nature, 2011, 473(7347): 317-325
CrossRef Google scholar
[2]
HanssonGK, HermanssonA. The immune system in atherosclerosis. Nat Immunol, 2011, 12(3): 204-212
CrossRef Google scholar
[3]
FanJ, WatanabeT. Atherosclerosis: Known and unknown. Pathol Int, 2022, 72(3): 151-160
CrossRef Google scholar
[4]
FalkE. Pathogenesis of atherosclerosis. J Am Coll Cardiol, 2006, 47(8Suppl): C7-12
CrossRef Google scholar
[5]
DuanH, ZhangQ, LiuJ, et al.. Suppression of apoptosis in vascular endothelial cell, the promising way for natural medicines to treat atherosclerosis. Pharmacol Res, 2021, 168: 105599
CrossRef Google scholar
[6]
WolfD, LeyK. Immunity and Inflammation in Atherosclerosis. Circ Res, 2019, 124(2): 315-327
CrossRef Google scholar
[7]
MozziniC, GarbinU, Fratta PasiniAM, et al.. An exploratory look at NETosis in atherosclerosis. Intern Emerg Med, 2017, 12(1): 13-22
CrossRef Google scholar
[8]
GrootaertMOJ, MoulisM, RothL, et al.. Vascular smooth muscle cell death, autophagy and senescence in atherosclerosis. Cardiovasc Res, 2018, 114(4): 622-634
CrossRef Google scholar
[9]
LibbyP, BuringJE, BadimonL, et al.. Atherosclerosis. Nat Rev Dis Primers, 2019, 5(1): 56
CrossRef Google scholar
[10]
HuMJ, TanJS, JiangWY, et al.. The optimal percutaneous coronary intervention strategy for patients with ST-segment elevation myocardial infarction and multivessel disease: a pairwise and network meta-analysis. Ther Adv Chronic Dis, 2022, 13: 20406223221078088
CrossRef Google scholar
[11]
ChenW, SchilperoortM, CaoY, et al.. Macrophage-targeted nanomedicine for the diagnosis and treatment of atherosclerosis. Nat Rev Cardiol, 2022, 19(4): 228-249
CrossRef Google scholar
[12]
DaiT, HeW, YaoC, et al.. Applications of inorganic nanoparticles in the diagnosis and therapy of atherosclerosis. Biomater Sci, 2020, 8(14): 3784-3799
CrossRef Google scholar
[13]
ZhangN, XieX, ChenH, et al.. Stem cell-based therapies for atherosclerosis: perspectives and ongoing controversies. Stem Cells Dev, 2014, 23(15): 1731-1740
CrossRef Google scholar
[14]
GlassCK, WitztumJL. Atherosclerosis. the road ahead. Cell, 2001, 104(4): 503-516
CrossRef Google scholar
[15]
RochetteL, LorinJ, ZellerM, et al.. Nitric oxide synthase inhibition and oxidative stress in cardiovascular diseases: possible therapeutic targets?. Pharmacol Ther, 2013, 140(3): 239-257
CrossRef Google scholar
[16]
WitztumJL, LichtmanAH. The influence of innate and adaptive immune responses on atherosclerosis. Annu Rev Pathol, 2014, 9: 73-102
CrossRef Google scholar
[17]
MarzollaV, ArmaniA, MammiC, et al.. Essential role of ICAM-1 in aldosterone-induced atherosclerosis. Int J Cardiol, 2017, 232: 233-242
CrossRef Google scholar
[18]
JiaX, BaiX, YangX, et al.. VCAM-1-bmdmg peptide targeted cationic liposomes containing NLRP3 siRNA to modulate LDL transcytosis as a novel therapy for experimental atherosclerosis. Metabolism, 2022, 135: 155274
CrossRef Google scholar
[19]
GeorgakisMK, BernhagenJ, HeitmanLH, et al.. Targeting the CCL2-CCR2 axis for atheroprotection. Eur Heart J, 2022, 43(19): 1799-1808
CrossRef Google scholar
[20]
AielloRJ, BourassaPA, LindseyS, et al.. Monocyte chemoattractant protein-1 accelerates atherosclerosis in apolipoprotein E-deficient mice. Arterioscler Thromb Vasc Biol, 1999, 19(6): 1518-1525
CrossRef Google scholar
[21]
MantaCP, LeibingT, FriedrichM, et al.. Targeting of Scavenger Receptors Stabilin-1 and Stabilin-2 Ameliorates Atherosclerosis by a Plasma Proteome Switch Mediating Monocyte/Macrophage Suppression. Circulation, 2022, 146(23): 1783-1799
CrossRef Google scholar
[22]
ThorpE, SubramanianM, TabasI. The role of macrophages and dendritic cells in the clearance of apoptotic cells in advanced atherosclerosis. Eur J Immunol, 2011, 41(9): 2515-2518
CrossRef Google scholar
[23]
MyasoedovaVA, ChistiakovDA, GrechkoAV, et al.. Matrix metalloproteinases in pro-atherosclerotic arterial remodeling. J Mol Cell Cardiol, 2018, 123: 159-167
CrossRef Google scholar
[24]
SaigusaR, WinkelsH, LeyK. T cell subsets and functions in atherosclerosis. Nat Rev Cardiol, 2020, 17(7): 387-401
CrossRef Google scholar
[25]
BotI, DaissormontIT, ZerneckeA, et al.. CXCR4 blockade induces atherosclerosis by affecting neutrophil function. J Mol Cell Cardiol, 2014, 74: 44-52
CrossRef Google scholar
[26]
HofheinzK, SeibertF, AckermannJA, et al.. Formation of atherosclerotic lesions is independent of eosinophils in male mice. Atherosclerosis, 2020, 311: 67-72
CrossRef Google scholar
[27]
ZhuJ, LiuB, WangZ, et al.. Exosomes from nicotine-stimulated macrophages accelerate atherosclerosis through miR-21-3p/PTEN-mediated VSMC migration and proliferation. Theranostics, 2019, 9(23): 6901-6919
CrossRef Google scholar
[28]
MonkBA, GeorgeSJ. The Effect of Ageing on Vascular Smooth Muscle Cell Behaviour— A Mini-Review. Gerontology, 2015, 61(5): 416-426
CrossRef Google scholar
[29]
BentzonJF, OtsukaF, VirmaniR, et al.. Mechanisms of plaque formation and rupture. Circ Res, 2014, 114(12): 1852-1866
CrossRef Google scholar
[30]
WeberC, BadimonL, MachF, et al.. Therapeutic strategies for atherosclerosis and atherothrombosis: Past, present and future. Thromb Haemost, 2017, 117(7): 1258-1264
CrossRef Google scholar
[31]
AliAH, YounisN, AbdallahR, et al.. Lipid-Lowering Therapies for Atherosclerosis: Statins, Fibrates, Ezetimibe and PCSK9 Monoclonal Antibodies. Curr Med Chem, 2021, 28(36): 7427-7445
CrossRef Google scholar
[32]
PastaA, CremoniniAL, PisciottaL, et al.. PCSK9 inhibitors for treating hypercholesterolemia. Expert Opin Pharmacother, 2020, 21(3): 353-363
CrossRef Google scholar
[33]
AlbersJJ, MarcovinaSM, ImperatoreG, et al.. Prevalence and determinants of elevated apolipoprotein B and dense low-density lipoprotein in youths with type 1 and type 2 diabetes. J Clin Endocrinol Metab, 2008, 93(3): 735-742
CrossRef Google scholar
[34]
HagensenMK, MortensenMB, KjolbyM, et al.. Increased retention of LDL from type 1 diabetic patients in atherosclerosis-prone areas of the murine arterial wall. Atherosclerosis, 2019, 286: 156-162
CrossRef Google scholar
[35]
TabitCE, ShenoudaSM, HolbrookM, et al.. Protein kinase C-β contributes to impaired endothelial insulin signaling in humans with diabetes mellitus. Circulation, 2013, 127(1): 86-95
CrossRef Google scholar
[36]
RidkerPM, EverettBM, ThurenT, et al.. Antiinflammatory Therapy with Canakinumab for Atherosclerotic Disease. N Engl J Med, 2017, 377(12): 1119-1131
CrossRef Google scholar
[37]
Lv N, Zhang Y, Wang L, et al. LncRNA/CircRNA-miRNA-mRNA Axis in Atherosclerotic Inflammation: Research Progress. Curr Pharm Biotechnol, 2023, doi: https://doi.org/10.2174/0113892010267577231005102901
[38]
CahillPA, RedmondEM. Vascular endothelium — Gatekeeper of vessel health. Atherosclerosis, 2016, 248: 97-109
CrossRef Google scholar
[39]
LinX, OuyangS, ZhiC, et al.. Focus on ferroptosis, pyroptosis, apoptosis and autophagy of vascular endothelial cells to the strategic targets for the treatment of atherosclerosis. Arch Biochem Biophys, 2022, 715: 109098
CrossRef Google scholar
[40]
WangY, FanY, SongY, et al.. Angiotensin II induces apoptosis of cardiac microvascular endothelial cells via regulating PTP1B/PI3K/Akt pathway. In Vitro Cell Dev Biol Anim, 2019, 55(10): 801-811
CrossRef Google scholar
[41]
OuyangS, YouJ, ZhiC, et al.. Ferroptosis: the potential value target in atherosclerosis. Cell Death Dis, 2021, 12(8): 782
CrossRef Google scholar
[42]
ChenX, CaiQ, LiangR, et al.. Copper homeostasis and copper-induced cell death in the pathogenesis of cardiovascular disease and therapeutic strategies. Cell Death Dis, 2023, 14(2): 105
CrossRef Google scholar
[43]
HeB, NieQ, WangF, et al.. Role of pyroptosis in atherosclerosis and its therapeutic implications. J Cell Physiol, 2021, 236(10): 7159-7175
CrossRef Google scholar
[44]
WangH, LiuC, ZhaoY, et al.. Mitochondria regulation in ferroptosis. Eur J Cell Biol, 2020, 99(1): 151058
CrossRef Google scholar
[45]
StockwellBR, Friedmann AngeliJP, BayirH, et al.. Ferroptosis: A Regulated Cell Death Nexus Linking Metabolism, Redox Biology, and Disease. Cell, 2017, 171(2): 273-285
CrossRef Google scholar
[46]
JiangX, StockwellBR, ConradM. Ferroptosis: mechanisms, biology and role in disease. Nat Rev Mol Cell Biol, 2021, 22(4): 266-282
CrossRef Google scholar
[47]
YangWS, KimKJ, GaschlerMM, et al.. Peroxidation of polyunsaturated fatty acids by lipoxygenases drives ferroptosis. Proc Natl Acad Sci U S A, 2016, 113(34): E4966-75
CrossRef Google scholar
[48]
DollS, PronethB, TyurinaYY, et al.. ACSL4 dictates ferroptosis sensitivity by shaping cellular lipid composition. Nat Chem Biol, 2017, 13(1): 91-98
CrossRef Google scholar
[49]
FengH, SchorppK, JinJ, et al.. Transferrin Receptor Is a Specific Ferroptosis Marker. Cell Rep, 2020, 30(10): 3411-3423.e7
CrossRef Google scholar
[50]
DollS, FreitasFP, ShahR, et al.. FSP1 is a glutathione-independent ferroptosis suppressor. Nature, 2019, 575(7784): 693-698
CrossRef Google scholar
[51]
MaY, YiM, WangW, et al.. Oxidative degradation of dihydrofolate reductase increases CD38-mediated ferroptosis susceptibility. Cell Death Dis, 2022, 13(11): 944
CrossRef Google scholar
[52]
KraftVAN, BezjianCT, PfeifferS, et al.. GTP Cyclohydrolase 1/Tetrahydrobiopterin Counteract Ferroptosis through Lipid Remodeling. ACS Cent Sci, 2020, 6(1): 41-53
CrossRef Google scholar
[53]
WangY, ZhaoY, YeT, et al.. Ferroptosis Signaling and Regulators in Atherosclerosis. Front Cell Dev Biol, 2021, 9: 809457
CrossRef Google scholar
[54]
GuoZ, RanQ, RobertsLJ2nd, et al.. Suppression of atherogenesis by overexpression of glutathione peroxidase-4 in apolipoprotein E-deficient mice. Free Radic Biol Med, 2008, 44(3): 343-352
CrossRef Google scholar
[55]
ChenCJ, HuangHS, ChangWC. Inhibition of arachidonate metabolism in human epidermoid carcinoma a431 cells overexpressing phospholipid hydroperoxide glutathione peroxidase. J Biomed Sci, 2002, 9(5): 453-459
CrossRef Google scholar
[56]
GaoM, MonianP, QuadriN, et al.. Glutaminolysis and Transferrin Regulate Ferroptosis. Mol Cell, 2015, 59(2): 298-308
CrossRef Google scholar
[57]
MouY, ZhangL, LiuZ, et al.. Abundant expression of ferroptosis-related SAT1 is related to unfavorable outcome and immune cell infiltration in low-grade glioma. BMC Cancer, 2022, 22(1): 215
CrossRef Google scholar
[58]
ChuB, KonN, ChenD, et al.. ALOX12 is required for p53-mediated tumour suppression through a distinct ferroptosis pathway. Nat Cell Biol, 2019, 21(5): 579-591
CrossRef Google scholar
[59]
LiC, ChenJW, LiuZH, et al.. CTRP5 promotes transcytosis and oxidative modification of low-density lipoprotein and the development of atherosclerosis. Atherosclerosis, 2018, 278: 197-209
CrossRef Google scholar
[60]
GaoY, ChenB, WangR, et al.. Knockdown of RRM1 in tumor cells promotes radio-/chemotherapy induced ferroptosis by regulating p53 ubiquitination and p21-GPX4 signaling axis. Cell Death Discov, 2022, 8(1): 343
CrossRef Google scholar
[61]
KangR, KroemerG, TangD. The tumor suppressor protein p53 and the ferroptosis network. Free Radic Biol Med, 2019, 133: 162-168
CrossRef Google scholar
[62]
ZhangQ, LiuJ, DuanH, et al.. Activation of Nrf2/HO-1 signaling: An important molecular mechanism of herbal medicine in the treatment of atherosclerosis via the protection of vascular endothelial cells from oxidative stress. J Adv Res, 2021, 34: 43-63
CrossRef Google scholar
[63]
Linna-KuosmanenS, Tomas BoschV, MoreauPR, et al.. NRF2 is a key regulator of endothelial microRNA expression under proatherogenic stimuli. Cardiovasc Res, 2021, 117(5): 1339-1357
CrossRef Google scholar
[64]
SongX, LongD. Nrf2 and Ferroptosis: A New Research Direction for Neurodegenerative Diseases. Front Neurosci, 2020, 14: 267
CrossRef Google scholar
[65]
RuotsalainenAK, LappalainenJP, HeiskanenE, et al.. Nuclear factor E2-related factor 2 deficiency impairs atherosclerotic lesion development but promotes features of plaque instability in hypercholesterolaemic mice. Cardiovasc Res, 2019, 115(1): 243-254
CrossRef Google scholar
[66]
KerinsMJ, OoiA. The Roles of NRF2 in Modulating Cellular Iron Homeostasis. Antioxid Redox Signal, 2018, 29(17): 1756-1773
CrossRef Google scholar
[67]
MurphyAJ, SarrazyV, WangN, et al.. Deficiency of ATP-binding cassette transporter B6 in megakaryocyte progenitors accelerates atherosclerosis in mice. Arterioscler Thromb Vasc Biol, 2014, 34(4): 751-758
CrossRef Google scholar
[68]
MachlusKR, JohnsonKE, KulenthirarajanR, et al.. CCL5 derived from platelets increases megakaryocyte proplatelet formation. Blood, 2016, 127(7): 921-926
CrossRef Google scholar
[69]
ZhouY, QueKT, ZhangZ, et al.. Iron overloaded polarizes macrophage to proinflammation phenotype through ROS/acetyl-p53 pathway. Cancer Med, 2018, 7(8): 4012-4022
CrossRef Google scholar
[70]
HandaP, ThomasS, Morgan-StevensonV, et al.. Iron alters macrophage polarization status and leads to steatohepatitis and fibrogenesis. J Leukoc Biol, 2019, 105(5): 1015-1026
CrossRef Google scholar
[71]
KapralovAA, YangQ, DarHH, et al.. Redox lipid reprogramming commands susceptibility of macrophages and microglia to ferroptotic death. Nat Chem Biol, 2020, 16(3): 278-290
CrossRef Google scholar
[72]
SampilvanjilA, KarasawaT, YamadaN, et al.. Cigarette smoke extract induces ferroptosis in vascular smooth muscle cells. Am J Physiol Heart Circ Physiol, 2020, 318(3): H508-H518
CrossRef Google scholar
[73]
JiangQW, KailiD, FreemanJ, et al.. Diabetes inhibits corneal epithelial cell migration and tight junction formation in mice and human via increasing ROS and impairing Akt signaling. Acta Pharmacol Sin, 2019, 40(9): 1205-1211
CrossRef Google scholar
[74]
FengJ, WangJ, WangY, et al.. Oxidative Stress and Lipid Peroxidation: Prospective Associations Between Ferroptosis and Delayed Wound Healing in Diabetic Ulcers. Front Cell Dev Biol, 2022, 10: 898657
CrossRef Google scholar
[75]
ChengTL, ChenPK, HuangWK, et al.. Plasminogen/thrombomodulin signaling enhances VEGF expression to promote cutaneous wound healing. J Mol Med (Berl), 2018, 96(12): 1333-1344
CrossRef Google scholar
[76]
IcliB, WuW, OzdemirD, et al.. MicroRNA-615-5p Regulates Angiogenesis and Tissue Repair by Targeting AKT/eNOS (Protein Kinase B/Endothelial Nitric Oxide Synthase) Signaling in Endothelial Cells. Arterioscler Thromb Vasc Biol, 2019, 39(7): 1458-1474
CrossRef Google scholar
[77]
BaiT, LiM, LiuY, et al.. Inhibition of ferroptosis alleviates atherosclerosis through attenuating lipid peroxidation and endothelial dysfunction in mouse aortic endothelial cell. Free Radic Biol Med, 2020, 160: 92-102
CrossRef Google scholar
[78]
XiaoFJ, ZhangD, WuY, et al.. miRNA-17-92 protects endothelial cells from erastin-induced ferroptosis through targeting the A20–ACSL4 axis. Biochem Biophys Res Commun, 2019, 515(3): 448-454
CrossRef Google scholar
[79]
YouJ, OuyangS, XieZ, et al.. The suppression of hyperlipid diet-induced ferroptosis of vascular smooth muscle cells protests against atherosclerosis independent of p53/SCL7A11/GPX4 axis. J Cell Physiol, 2023, 238(8): 1891-1908
CrossRef Google scholar
[80]
LiuW, ÖstbergN, YalcinkayaM, et al.. Erythroid lineage Jak2V617F expression promotes atherosclerosis through erythrophagocytosis and macrophage ferroptosis. J Clin Invest, 2022, 132(13): e155724
CrossRef Google scholar
[81]
WangY, TangM. PM2.5 induces ferroptosis in human endothelial cells through iron overload and redox imbalance. Environ Pollut, 2019, 254: 112937 Pt A
CrossRef Google scholar
[82]
YaoX, XieR, CaoY, et al.. Simvastatin induced ferroptosis for triple-negative breast cancer therapy. J Nanobiotechnology, 2021, 19(1): 311
CrossRef Google scholar
[83]
ZhangQ, QuH, ChenY, et al.. Atorvastatin Induces Mitochondria-Dependent Ferroptosis via the Modulation of Nrf2-xCT/GPx4 Axis. Front Cell Dev Biol, 2022, 10: 806081
CrossRef Google scholar
[84]
JiaoY, ZhangT, ZhangC, et al.. Exosomal miR-30d-5p of neutrophils induces M1 macrophage polarization and primes macrophage pyroptosis in sepsis-related acute lung injury. Crit Care, 2021, 25(1): 356
CrossRef Google scholar
[85]
RobinsonKS, TohGA, RozarioP, et al.. ZAKa-driven ribotoxic stress response activates the human NLRP1 inflammasome. Science, 2022, 377(6603): 328-335
CrossRef Google scholar
[86]
YuP, ZhangX, LiuN, et al.. Pyroptosis: mechanisms and diseases. Signal Transduct Target Ther, 2021, 6(1): 128
CrossRef Google scholar
[87]
HeX, FanX, BaiB, et al.. Pyroptosis is a critical immune-inflammatory response involved in atherosclerosis. Pharmacol Res, 2021, 165: 105447
CrossRef Google scholar
[88]
ZahidMDK, RogowskiM, PonceC, et al.. CCAAT/enhancer-binding protein beta (C/EBPβ) knockdown reduces inflammation, ER stress, and apoptosis, and promotes autophagy in oxLDL-treated RAW264.7 macrophage cells. Mol Cell Biochem, 2020, 463(1–2): 211-223
CrossRef Google scholar
[89]
ChenS, ZuoY, HuangL, et al.. The MC(4) receptor agonist RO27-3225 inhibits NLRP1-dependent neuronal pyroptosis via the ASK1/JNK/p38 MAPK pathway in a mouse model of intracerebral haemorrhage. Br J Pharmacol, 2019, 176(9): 1341-1356
CrossRef Google scholar
[90]
HeQ, YouH, LiXM, et al.. HMGB1 promotes the synthesis of pro-IL-1β and pro-IL-18 by activation of p38 MAPK and NF-κB through receptors for advanced glycation end-products in macrophages. Asian Pac J Cancer Prev, 2012, 13(4): 1365-1370
CrossRef Google scholar
[91]
BaiW, HuoT, ChenX, et al.. Sacubitril/valsartan inhibits ox-LDL-induced MALAT1 expression, inflammation and apoptosis by suppressing the TLR4/NF-κB signaling pathway in HUVECs. Mol Med Rep, 2021, 23(6): 402
CrossRef Google scholar
[92]
ZhangM, XueY, ChenH, et al.. Resveratrol Inhibits MMP3 and MMP9 Expression and Secretion by Suppressing TLR4/NF-κB/STAT3 Activation in Ox-LDL-Treated HUVECs. Oxid Med Cell Longev, 2019, 2019: 9013169
[93]
YangY, WangH, KouadirM, et al.. Recent advances in the mechanisms of NLRP3 inflammasome activation and its inhibitors. Cell Death Dis, 2019, 10(2): 128
CrossRef Google scholar
[94]
SuJ, ZhouH, LiuX, et al.. oxLDL antibody inhibits MCP-1 release in monocytes/macrophages by regulating Ca(2+) /K(+) channel flow. J Cell Mol Med, 2017, 21(5): 929-940
CrossRef Google scholar
[95]
LiHX, KongFJ, BaiSZ, et al.. Involvement of calcium-sensing receptor in oxLDL-induced MMP-2 production in vascular smooth muscle cells via PI3K/Akt pathway. Mol Cell Biochem, 2012, 362(1–2): 115-122
[96]
ZhanX, LiQ, XuG, et al.. The mechanism of NLRP3 inflammasome activation and its pharmacological inhibitors. Front Immunol, 2022, 13: 1109938
CrossRef Google scholar
[97]
ZhaolinZ, JiaojiaoC, PengW, et al.. OxLDL induces vascular endothelial cell pyroptosis through miR-125a-5p/TET2 pathway. J Cell Physiol, 2019, 234(5): 7475-7491
CrossRef Google scholar
[98]
WangY, ShiP, ChenQ, et al.. Mitochondrial ROS promote macrophage pyroptosis by inducing GSDMD oxidation. J Mol Cell Biol, 2019, 11(12): 1069-1082
CrossRef Google scholar
[99]
ZhangX, ZhangJH, ChenXY, et al.. Reactive oxygen species-induced TXNIP drives fructose-mediated hepatic inflammation and lipid accumulation through NLRP3 inflammasome activation. Antioxid Redox Signal, 2015, 22(10): 848-870
CrossRef Google scholar
[100]
YangF, QinY, WangY, et al.. Metformin Inhibits the NLRP3 Inflammasome via AMPK/mTOR-dependent Effects in Diabetic Cardiomyopathy. Int J Biol Sci, 2019, 15(5): 1010-1019
CrossRef Google scholar
[101]
LuY, LuY, MengJ, et al.. Pyroptosis and Its Regulation in Diabetic Cardiomyopathy. Front Physiol, 2021, 12: 791848
CrossRef Google scholar
[102]
YouL, ZhengY, YangJ, et al.. LncRNA MDRL Mitigates Atherosclerosis through miR-361/SQSTM1/NLRP3 Signaling. Mediators Inflamm, 2022, 2022: 5463505
CrossRef Google scholar
[103]
AhmadiA, ArgulianE, LeipsicJ, et al.. From Subclinical Atherosclerosis to Plaque Progression and Acute Coronary Events: JACC State-of-the-Art Review. J Am Coll Cardiol, 2019, 74(12): 1608-1617
CrossRef Google scholar
[104]
KhanR, RheaumeE, TardifJC. Examining the Role of and Treatment Directed at IL-1β in Atherosclerosis. Curr Atheroscler Rep, 2018, 20(11): 53
CrossRef Google scholar
[105]
WuQ, HeX, WuLM, et al.. MLKL Aggravates Ox-LDL-Induced Cell Pyroptosis via Activation of NLRP3 Inflammasome in Human Umbilical Vein Endothelial Cells. Inflammation, 2020, 43(6): 2222-2231
CrossRef Google scholar
[106]
HuangP, LiuW, ChenJ, et al.. TRIM31 inhibits NLRP3 inflammasome and pyroptosis of retinal pigment epithelial cells through ubiquitination of NLRP3. Cell Biol Int, 2020, 44(11): 2213-2219
CrossRef Google scholar
[107]
ChenJ, ZhangC, YanT, et al.. Atorvastatin ameliorates early brain injury after subarachnoid hemorrhage via inhibition of pyroptosis and neuroinflammation. J Cell Physiol, 2021, 236(10): 6920-6931
CrossRef Google scholar
[108]
WuLM, WuSG, ChenF, et al.. Atorvastatin inhibits pyroptosis through the lncRNA NEXN-AS1/NEXN pathway in human vascular endothelial cells. Atherosclerosis, 2020, 293: 26-34
CrossRef Google scholar
[109]
MaS, ChenJ, FengJ, et al.. Melatonin Ameliorates the Progression of Atherosclerosis via Mitophagy Activation and NLRP3 Inflammasome Inhibition. Oxid Med Cell Longev, 2018, 2018: 9286458
CrossRef Google scholar
[110]
XingSS, YangJ, LiWJ, et al.. Salidroside Decreases Atherosclerosis Plaque Formation via Inhibiting Endothelial Cell Pyroptosis. Inflammation, 2020, 43(2): 433-440
CrossRef Google scholar
[111]
HanY, QiuH, PeiX, et al.. Low-dose Sinapic Acid Abates the Pyroptosis of Macrophages by Downregulation of lncRNA-MALAT1 in Rats With Diabetic Atherosclerosis. J Cardiovasc Pharmacol, 2018, 71(2): 104-112
CrossRef Google scholar
[112]
HuQ, ZhangT, YiL, et al.. Dihydromyricetin inhibits NLRP3 inflammasome-dependent pyroptosis by activating the Nrf2 signaling pathway in vascular endothelial cells. Biofactors, 2018, 44(2): 123-136
CrossRef Google scholar
[113]
MartinetW, SchrijversDM, HermanAG, et al.. z-VAD-fmk-induced non-apoptotic cell death of macrophages: possibilities and limitations for atherosclerotic plaque stabilization. Autophagy, 2006, 2(4): 312-314
CrossRef Google scholar
[114]
ChenJ, JiangY, ShiH, et al.. The molecular mechanisms of copper metabolism and its roles in human diseases. Pflugers Arch, 2020, 472(10): 1415-1429
CrossRef Google scholar
[115]
TsvetkovP, CoyS, PetrovaB, et al.. Copper induces cell death by targeting lipoylated TCA cycle proteins. Science, 2022, 375(6586): 1254-1261
CrossRef Google scholar
[116]
RuizLM, LibedinskyA, ElorzaAA. Role of Copper on Mitochondrial Function and Metabolism. Front Mol Biosci, 2021, 8: 711227
CrossRef Google scholar
[117]
ZhangZ, WeichenthalS, KwongJC, et al.. A Population-Based Cohort Study of Respiratory Disease and LongTerm Exposure to Iron and Copper in Fine Particulate Air Pollution and Their Combined Impact on Reactive Oxygen Species Generation in Human Lungs. Environ Sci Technol, 2021, 55(6): 3807-3818
CrossRef Google scholar
[118]
KoksalC, ErcanM, BozkurtAK, et al.. Abdominal aortic aneurysm or aortic occlusive disease: role of trace element imbalance. Angiology, 2007, 58(2): 191-195
CrossRef Google scholar
[119]
ItohS, KimHW, NakagawaO, et al.. Novel role of antioxidant-1 (Atox1) as a copper-dependent transcription factor involved in cell proliferation. J Biol Chem, 2008, 283(14): 9157-9167
CrossRef Google scholar
[120]
DasA, SudhaharV, Ushio-FukaiM, et al.. Novel interaction of antioxidant-1 with TRAF4: role in inflammatory responses in endothelial cells. Am J Physiol Cell Physiol, 2019, 317(6): C1161-C1171
CrossRef Google scholar
[121]
WeiH, ZhangWJ, McMillenTS, et al.. Copper chelation by tetrathiomolybdate inhibits vascular inflammation and atherosclerotic lesion development in apolipoprotein E-deficient mice. Atherosclerosis, 2012, 223(2): 306-313
CrossRef Google scholar
[122]
AlvarezHM, XueY, RobinsonCD, et al.. Tetrathiomolybdate inhibits copper trafficking proteins through metal cluster formation. Science, 2010, 327(5963): 331-334
CrossRef Google scholar
[123]
Vieceli Dalla SegaF, FortiniF, AquilaG, et al.. Notch Signaling Regulates Immune Responses in Atherosclerosis. Front Immunol, 2019, 10: 1130
CrossRef Google scholar
[124]
BraySJ. Notch signalling: a simple pathway becomes complex. Nat Rev Mol Cell Biol, 2006, 7(9): 678-689
CrossRef Google scholar
[125]
LiH, ZhaoL, WangT, et al.. Dietary Cholesterol Supplements Disturb Copper Homeostasis in Multiple Organs in Rabbits: Aorta Copper Concentrations Negatively Correlate with the Severity of Atherosclerotic Lesions. Biol Trace Elem Res, 2022, 200(1): 164-171
CrossRef Google scholar
[126]
BügelS, HarperA, RockE, et al.. Effect of copper supplementation on indices of copper status and certain CVD risk markers in young healthy women. Br J Nutr, 2005, 94(2): 231-236
CrossRef Google scholar
[127]
FortiniF, Vieceli Dalla SegaF, CalicetiC, et al.. Estrogen receptor β-dependent Notchl activation protects vascular endothelium against tumor necrosis factor a (TNFa)-induced apoptosis. J Biol Chem, 2017, 292(44): 18178-18191
CrossRef Google scholar
[128]
FortiniF, Vieceli Dalla SegaF, CalicetiC, et al.. Estrogen-mediated protection against coronary heart disease: The role of the Notch pathway. J Steroid Biochem Mol Biol, 2019, 189: 87-100
CrossRef Google scholar
[129]
Martos-RodríguezCJ, Albarrán-JuárezJ, Morales-CanoD, et al.. Fibrous Caps in Atherosclerosis Form by Notch-Dependent Mechanisms Common to Arterial Media Development. Arterioscler Thromb Vasc Biol, 2021, 41(9): e427-e439
CrossRef Google scholar
[130]
GreenDR. The Coming Decade of Cell Death Research: Five Riddles. Cell, 2019, 177(5): 1094-1107
CrossRef Google scholar
[131]
TaoX, WanX, WuD, et al.. A tandem activation of NLRP3 inflammasome induced by copper oxide nanoparticles and dissolved copper ion in J774A.1 macrophage. J Hazard Mater, 2021, 411: 125134
CrossRef Google scholar
[132]
MehrotraP, RavichandranKS. Drugging the efferocytosis process: concepts and opportunities. Nat Rev Drug Discov, 2022, 21(8): 601-620
CrossRef Google scholar
[133]
PertiwiKR, de BoerOJ, MackaaijC, et al.. Extracellular traps derived from macrophages, mast cells, eosinophils and neutrophils are generated in a time-dependent manner during atherothrombosis. J Pathol, 2019, 247(4): 505-512
CrossRef Google scholar
[134]
MitraS, DeshmukhA, SachdevaR, et al.. Oxidized low-density lipoprotein and atherosclerosis implications in antioxidant therapy. Am J Med Sci, 2011, 342(2): 135-142
CrossRef Google scholar
[135]
LeeC, ChengW, ChangM, et al.. Hypoxia-induced apoptosis in endothelial cells and embryonic stem cells. Apoptosis, 2005, 10(4): 887-894
CrossRef Google scholar
[136]
ZhangY, XieY, YouS, et al.. Autophagy and Apoptosis in the Response of Human Vascular Endothelial Cells to Oxidized Low-Density Lipoprotein. Cardiology, 2015, 132(1): 27-33
CrossRef Google scholar
[137]
HensonPM. Cell Removal: Efferocytosis. Annu Rev Cell Dev Biol, 2017, 33: 127-144
CrossRef Google scholar
[138]
MoriokaS, MaueröderC, RavichandranKS. Living on the Edge: Efferocytosis at the Interface of Homeostasis and Pathology. Immunity, 2019, 50(5): 1149-1162
CrossRef Google scholar
[139]
LauberK, BohnE, KröberSM, et al.. Apoptotic cells induce migration of phagocytes via caspase-3-mediated release of a lipid attraction signal. Cell, 2003, 113(6): 717-730
CrossRef Google scholar
[140]
ElliottMR, ChekeniFB, TrampontPC, et al.. Nucleotides released by apoptotic cells act as a find-me signal to promote phagocytic clearance. Nature, 2009, 461(7261): 282-286
CrossRef Google scholar
[141]
SegawaK, KurataS, YanagihashiY, et al.. Caspase-mediated cleavage of phospholipid flippase for apoptotic phosphatidylserine exposure. Science, 2014, 344(6188): 1164-1168
CrossRef Google scholar
[142]
SuzukiJ, DenningDP, ImanishiE, et al.. Xk-related - protein 8 and CED-8 promote phosphatidylserine exposure in apoptotic cells. Science, 2013, 341(6144): 403-406
CrossRef Google scholar
[143]
OkaK, SawamuraT, KikutaK, et al.. Lectin-like oxidized low-density lipoprotein receptor 1 mediates phagocytosis of aged/apoptotic cells in endothelial cells. Proc Natl Acad Sci USA, 1998, 95(16): 9535-9540
CrossRef Google scholar
[144]
ChangMK, BergmarkC, LaurilaA, et al.. Monoclonal antibodies against oxidized low-density lipoprotein bind to apoptotic cells and inhibit their phagocytosis by elicited macrophages: evidence that oxidation-specific epitopes mediate macrophage recognition. Proc Natl Acad Sci USA, 1999, 96(11): 6353-6358
CrossRef Google scholar
[145]
BarclayAN, Van den BergTK. The interaction between signal regulatory protein alpha (SIRPa) and CD47: structure, function, and therapeutic target. Annu Rev Immunol, 2014, 32: 25-50
CrossRef Google scholar
[146]
Nakahashi-OdaC, FujiyamaS, NakazawaY, et al.. CD300a blockade enhances efferocytosis by infiltrating myeloid cells and ameliorates neuronal deficit after ischemic stroke. Sci Immunol, 2021, 6(64): eabe7915
CrossRef Google scholar
[147]
GreenDR, OguinTH, MartinezJ. The clearance of dying cells: table for two. Cell Death Differ, 2016, 23(6): 915-926
CrossRef Google scholar
[148]
HeckmannBL, GreenDR. LC3-associated phagocytosis at a glance. J Cell Sci, 2019, 132(5): jcs222984
CrossRef Google scholar
[149]
ThorpE, VaisarT, SubramanianM, et al.. Shedding of the Mer tyrosine kinase receptor is mediated by ADAM17 protein through a pathway involving reactive oxygen species, protein kinase CS, and p38 mitogen-activated protein kinase (MAPK). J Biol Chem, 2011, 286(38): 33335-33344
CrossRef Google scholar
[150]
KomuraH, MiksaM, WuR, et al.. Milk fat globule epidermal growth factor-factor VIII is down-regulated in sepsis via the lipopolysaccharide-CD14 pathway. J Immunol, 2009, 182(1): 581-587
CrossRef Google scholar
[151]
KawaiT, ElliottKJ, ScaliaR, et al.. Contribution of ADAM17 and related ADAMs in cardiovascular diseases. Cell Mol Life Sci, 2021, 78(9): 4161-4187
CrossRef Google scholar
[152]
ZhangY, WangY, ZhouD, et al.. Angiotensin II deteriorates advanced atherosclerosis by promoting MerTK cleavage and impairing efferocytosis through the AT(1)R/ROS/p38 MAPK/ADAM17 pathway. Am J Physiol Cell Physiol, 2019, 317(4): C776-C787
CrossRef Google scholar
[153]
NandaV, DowningKP, YeJ, et al.. CDKN2B Regulates TGFβ Signaling and Smooth Muscle Cell Investment of Hypoxic Neovessels. Circ Res, 2016, 118(2): 230-240
CrossRef Google scholar
[154]
LeeperNJ, RaiesdanaA, KojimaY, et al.. Loss of CDKN2B promotes p53-dependent smooth muscle cell apoptosis and aneurysm formation. Arterioscler Thromb Vasc Biol, 2013, 33(1): e1-e10
CrossRef Google scholar
[155]
SinglaB, LinHP, AhnW, et al.. Loss of myeloid cell-specific SIRPa, but not CD47, attenuates inflammation and suppresses atherosclerosis. Cardiovasc Res, 2022, 118(15): 3097-3111
CrossRef Google scholar
[156]
SchrijversDM, De MeyerGR, HermanAG, et al.. Phagocytosis in atherosclerosis: Molecular mechanisms and implications for plaque progression and stability. Cardiovasc Res, 2007, 73(3): 470-480
CrossRef Google scholar
[157]
ShawPX, HörkköS, TsimikasS, et al.. Human-derived anti-oxidized LDL autoantibody blocks uptake of oxidized LDL by macrophages and localizes to atherosclerotic lesions in vivo.. Arterioscler Thromb Vasc Biol, 2001, 21(8): 1333-1339
CrossRef Google scholar
[158]
MartinetW, SchrijversDM, De MeyerGR. Necrotic cell death in atherosclerosis. Basic Res Cardiol, 2011, 106(5): 749-760
CrossRef Google scholar
[159]
SchrijversDM, De MeyerGR, KockxMM, et al.. Phagocytosis of apoptotic cells by macrophages is impaired in atherosclerosis. Arterioscler Thromb Vasc Biol, 2005, 25(6): 1256-1261
CrossRef Google scholar
[160]
KojimaY, DowningK, KunduR, et al.. Cyclin-dependent kinase inhibitor 2B regulates efferocytosis and atherosclerosis. J Clin Invest, 2014, 124(3): 1083-1097
CrossRef Google scholar
[161]
ProtoJD, DoranAC, GusarovaG, et al.. Regulatory T Cells Promote Macrophage Efferocytosis during Inflammation Resolution. Immunity, 2018, 49(4): 666-677.e6
CrossRef Google scholar
[162]
WeiYT, WangXR, YanC, et al.. Thymosin a-l Reverses M2 Polarization of Tumor-Associated Macrophages during Efferocytosis. Cancer Res, 2022, 82(10): 1991-2002
CrossRef Google scholar
[163]
ChenW, LiL, WangJ, et al.. The ABCA1-efferocytosis axis: A new strategy to protect against atherosclerosis. Clin Chim Acta, 2021, 518: 1-8
CrossRef Google scholar
[164]
YurdagulAJr.. Crosstalk Between Macrophages and Vascular Smooth Muscle Cells in Atherosclerotic Plaque Stability. Arterioscler Thromb Vasc Biol, 2022, 42(4): 372-380
CrossRef Google scholar
[165]
CaiB, ThorpEB, DoranAC, et al.. MerTK receptor cleavage promotes plaque necrosis and defective resolution in atherosclerosis. J Clin Invest, 2017, 127(2): 564-568
CrossRef Google scholar
[166]
Ait-OufellaH, KinugawaK, ZollJ, et al.. Lactadherin deficiency leads to apoptotic cell accumulation and accelerated atherosclerosis in mice. Circulation, 2007, 115(16): 2168-2177
CrossRef Google scholar
[167]
WeiY, ZhuM, Corbalán-CamposJ, et al.. Regulation of Csf1r and Bcl6 in macrophages mediates the stage-specific effects of microRNA-155 on atherosclerosis. Arterioscler Thromb Vasc Biol, 2015, 35(4): 796-803
CrossRef Google scholar
[168]
KhannaS, BiswasS, ShangY, et al.. Macrophage dysfunction impairs resolution of inflammation in the wounds of diabetic mice. PLoS One, 2010, 5(3): e9539
CrossRef Google scholar
[169]
MahmoudiA, FirouzjaeiAA, DarijaniF, et al.. Effect of diabetes on efferocytosis process. Mol Biol Rep, 2022, 49(11): 10849-10863
CrossRef Google scholar
[170]
PetkovicA, ErcegS, MunjasJ, et al.. LncRNAs as Regulators of Atherosclerotic Plaque Stability. Cells, 2023, 12(14): 1832
CrossRef Google scholar
[171]
YeZM, YangS, XiaYP, et al.. LncRNA MIAT sponges miR-149-5p to inhibit efferocytosis in advanced atherosclerosis through CD47 upregulation. Cell Death Dis, 2019, 10(2): 138
CrossRef Google scholar
[172]
KojimaY, VolkmerJP, McKennaK, et al.. CD47-blocking antibodies restore phagocytosis and prevent atherosclerosis. Nature, 2016, 536(7614): 86-90
CrossRef Google scholar
[173]
GerlachBD, MarinelloM, HeinzJ, et al.. Resolvin D1 promotes the targeting and clearance of necroptotic cells. Cell Death Differ, 2020, 27(2): 525-539
CrossRef Google scholar
[174]
AzcutiaV, RoutledgeM, WilliamsMR, et al.. CD47 plays a critical role in T-cell recruitment by regulation of LFA-1 and VLA-4 integrin adhesive functions. Mol Biol Cell, 2013, 24(21): 3358-3368
CrossRef Google scholar
[175]
Tosello-TrampontAC, Nakada-TsukuiK, RavichandranKS. Engulfment of apoptotic cells is negatively regulated by Rho-mediated signaling. J Biol Chem, 2003, 278(50): 49911-49919
CrossRef Google scholar
[176]
WuDJ, XuJZ, WuYJ, et al.. Effects of fasudil on early atherosclerotic plaque formation and established lesion progression in apolipoprotein E-knockout mice. Atherosclerosis, 2009, 207(1): 68-73
CrossRef Google scholar
[177]
FloresAM, Hosseini-NassabN, JarrKU, et al.. Proefferocytic nanoparticles are specifically taken up by lesional macrophages and prevent atherosclerosis. Nat Nanotechnol, 2020, 15(2): 154-161
CrossRef Google scholar
[178]
DöringY, SoehnleinO, WeberC. Neutrophil Extracellular Traps in Atherosclerosis and Atherothrombosis. Circ Res, 2017, 120(4): 736-743
CrossRef Google scholar
[179]
YippBG, PetriB, SalinaD, et al.. Infection-induced NETosis is a dynamic process involving neutrophil multitasking in vivo.. Nat Med, 2012, 18(9): 1386-1393
CrossRef Google scholar
[180]
PilsczekFH, SalinaD, PoonKK, et al.. A novel mechanism of rapid nuclear neutrophil extracellular trap formation in response to Staphylococcus aureus. J Immunol, 2010, 185(12): 7413-7425
CrossRef Google scholar
[181]
BrinkmannV, ReichardU, GoosmannC, et al.. Neutrophil extracellular traps kill bacteria. Science, 2004, 303(5663): 1532-1535
CrossRef Google scholar
[182]
NakazawaD, DesaiJ, SteigerS, et al.. Activated platelets induce MLKL-driven neutrophil necroptosis and release of neutrophil extracellular traps in venous thrombosis. Cell Death Discov, 2018, 4: 6
CrossRef Google scholar
[183]
SchreiberA, RousselleA, BeckerJU, et al.. Necroptosis controls NET generation and mediates complement activation, endothelial damage, and autoimmune vasculitis. Proc Natl Acad Sci USA, 2017, 114(45): E9618-E9625
CrossRef Google scholar
[184]
ChenKW, MonteleoneM, BoucherD, et al.. Noncanonical inflammasome signaling elicits gasdermin D-dependent neutrophil extracellular traps. Sci Immunol, 2018, 3(26): eaar6676
CrossRef Google scholar
[185]
QuillardT, AraújoHA, FranckG, et al.. TLR2 and neutrophils potentiate endothelial stress, apoptosis and detachment: implications for superficial erosion. Eur Heart J, 2015, 36(22): 1394-1404
CrossRef Google scholar
[186]
PertiwiKR, van der WalAC, PabitteiDR, et al.. Neutrophil Extracellular Traps Participate in All Different Types of Thrombotic and Haemorrhagic Complications of Coronary Atherosclerosis. Thromb Haemost, 2018, 118(6): 1078-1087
CrossRef Google scholar
[187]
Carmona-RiveraC, ZhaoW, YalavarthiS, et al.. Neutrophil extracellular traps induce endothelial dysfunction in systemic lupus erythematosus through the activation of matrix metalloproteinase-2. Ann Rheum Dis, 2015, 74(7): 1417-1424
CrossRef Google scholar
[188]
DöringY, MantheyHD, DrechslerM, et al.. Auto-antigenic protein-DNA complexes stimulate plasmacytoid dendritic cells to promote atherosclerosis. Circulation, 2012, 125(13): 1673-1683
CrossRef Google scholar
[189]
ChenHJ, TasSW, de WintherMPJ. Type-I interferons in atherosclerosis. J Exp Med, 2020, 217(1): e20190459
CrossRef Google scholar
[190]
DingX, XiangW, HeX. IFN-I Mediates Dysfunction of Endothelial Progenitor Cells in Atherosclerosis of Systemic Lupus Erythematosus. Front Immunol, 2020, 11: 581385
CrossRef Google scholar
[191]
BorissoffJI, JoosenIA, VersteylenMO, et al.. Elevated levels of circulating DNA and chromatin are independently associated with severe coronary atherosclerosis and a prothrombotic state. Arterioscler Thromb Vasc Biol, 2013, 33(8): 2032-2040
CrossRef Google scholar
[192]
ZhaiM, GongS, LuanP, et al.. Extracellular traps from activated vascular smooth muscle cells drive the progression of atherosclerosis. Nat Commun, 2022, 13(1): 7500
CrossRef Google scholar
[193]
ZhangYG, SongY, GuoXL, et al.. Exosomes derived from oxLDL-stimulated macrophages induce neutrophil extracellular traps to drive atherosclerosis. Cell Cycle, 2019, 18(20): 2674-2684
CrossRef Google scholar
[194]
WangW, JinY, ZengN, et al.. SOD2 Facilitates the Antiviral Innate Immune Response by Scavenging Reactive Oxygen Species. Viral Immunol, 2017, 30(8): 582-589
CrossRef Google scholar
[195]
ChenL, HuL, LiQ, et al.. Exosome-encapsulated miR-505 from ox-LDL-treated vascular endothelial cells aggravates atherosclerosis by inducing NET formation. Acta Biochim Biophys Sin (Shanghai), 2019, 51(12): 1233-1241
CrossRef Google scholar
[196]
WarnatschA, IoannouM, WangQ, et al.. Inflammation. Neutrophil extracellular traps license macrophages for cytokine production in atherosclerosis. Science, 2015, 349(6245): 316-320
CrossRef Google scholar
[197]
DavisJCJr., ManziS, YarboroC, et al.. Recombinant human Dnase I (rhDNase) in patients with lupus nephritis. Lupus, 1999, 8(1): 68-76
CrossRef Google scholar
[198]
LiN, ZhengX, ChenM, et al.. Deficient DNASE1L3 facilitates neutrophil extracellular traps-induced invasion via cyclic GMP-AMP synthase and the non-canonical NF-κB pathway in diabetic hepatocellular carcinoma. Clin Transl Immunology, 2022, 11(4): e1386
CrossRef Google scholar
[199]
RohrbachAS, SladeDJ, ThompsonPR, et al.. Activation of PAD4 in NET formation. Front Immunol, 2012, 3: 360
CrossRef Google scholar
[200]
KnightJS, LuoW, O’DellAA, et al.. Peptidylargmme deiminase inhibition reduces vascular damage and modulates innate immune responses in murine models of atherosclerosis. Circ Res, 2014, 114(6): 947-956
CrossRef Google scholar
[201]
ChenYR, XiangXD, SunF, et al.. Simvastatin Reduces NETosis to Attenuate Severe Asthma by Inhibiting PAD4 Expression. Oxid Med Cell Longev, 2023, 2023: 1493684
CrossRef Google scholar
[202]
Al-GhoulWM, KimMS, FazalN, et al.. Evidence for simvastatin anti-inflammatory actions based on quantitative analyses of NETosis and other inflam-mation/oxidation markers. Results Immunol, 2014, 4: 14-22
CrossRef Google scholar
[203]
HuangSU, O’SullivanKM. The Expanding Role of Extracellular Traps in Inflammation and Autoimmunity: The New Players in Casting Dark Webs. Int J Mol Sci, 2022, 23(7): 3793
CrossRef Google scholar
[204]
YousefiS, MihalacheC, KozlowskiE, et al.. Viable neutrophils release mitochondrial DNA to form neutrophil extracellular traps. Cell Death Differ, 2009, 16(11): 1438-1444
CrossRef Google scholar
[205]
KeshariRS, JyotiA, DubeyM, et al.. Cytokines induced neutrophil extracellular traps formation: implication for the inflammatory disease condition. PLoS One, 2012, 7(10): e48111
CrossRef Google scholar
[206]
KnightJS, Carmona-RiveraC, KaplanMJ. Proteins derived from neutrophil extracellular traps may serve as self-antigens and mediate organ damage in autoimmune diseases. Front Immunol, 2012, 3: 380
CrossRef Google scholar
[207]
CsomósK, KristófE, JakobB, et al.. Protein cross-linking by chlorinated polyamines and transglutamylation stabilizes neutrophil extracellular traps. Cell Death Dis, 2016, 7(8): e2332
CrossRef Google scholar
[208]
KingPT, SharmaR, O’SullivanK, et al.. Nontypeable Haemophilus influenzae induces sustained lung oxidative stress and protease expression. PLoS One, 2015, 10(3): e0120371
CrossRef Google scholar
[209]
LiuP, WuX, LiaoC, et al.. Escherichia coli and Candida albicans induced macrophage extracellular trap-like structures with limited microbicidal activity. PLoS One, 2014, 9(2): e90042
CrossRef Google scholar
[210]
KingPT, SharmaR, O’SullivanKM, et al.. Deoxyribonuclease 1 reduces pathogenic effects of cigarette smoke exposure in the lung. Sci Rep, 2017, 7(1): 12128
CrossRef Google scholar
[211]
O’SullivanKM, LoCY, SummersSA, et al.. Renal participation of myeloperoxidase in antineutrophil cytoplasmic antibody (ANCA)-associated glomerulonephritis. Kidney Int, 2015, 88(5): 1030-1046
CrossRef Google scholar
[212]
LauthX, von Köckritz-BlickwedeM, McNamaraCW, et al.. M1 protein allows Group A streptococcal survival in phagocyte extracellular traps through cathelicidin inhibition. J Innate Immun, 2009, 1(3): 202-214
CrossRef Google scholar
[213]
Garcia-RodríguezKM, BahriR, SattentauC, et al.. Human mast cells exhibit an individualized pattern of antimicrobial responses. Immun Inflamm Dis, 2020, 8(2): 198-210
CrossRef Google scholar
[214]
von Köckritz-BlickwedeM, GoldmannO, ThulinP, et al.. Phagocytosis-independent antimicrobial activity of mast cells by means of extracellular trap formation. Blood, 2008, 111(6): 3070-3080
CrossRef Google scholar
[215]
NijaRJ, SanjuS, SidharthanN, et al.. Extracellular Trap by Blood Cells: Clinical Implications. Tissue Eng Regen Med, 2020, 17(2): 141-153
CrossRef Google scholar
[216]
LinAM, RubinCJ, KhandpurR, et al.. Mast cells and neutrophils release IL-17 through extracellular trap formation in psoriasis. J Immunol, 2011, 187(1): 490-500
CrossRef Google scholar
[217]
YousefiS, GoldJA, AndinaN, et al.. Catapult-like release of mitochondrial DNA by eosinophils contributes to antibacterial defense. Nat Med, 2008, 14(9): 949-953
CrossRef Google scholar
[218]
UekiS, MeloRC, GhiranI, et al.. Eosinophil extracellular DNA trap cell death mediates lytic release of free secretion-competent eosinophil granules in humans. Blood, 2013, 121(11): 2074-2083
CrossRef Google scholar
[219]
YousefiS, MorshedM, AminiP, et al.. Basophils exhibit antibacterial activity through extracellular trap formation. Allergy, 2015, 70(9): 1184-1188
CrossRef Google scholar
[220]
LouresFV, RöhmM, LeeCK, et al.. Recognition of Aspergillus fumigatus hyphae by human plasmacytoid dendritic cells is mediated by dectin-2 and results in formation of extracellular traps. PLoS Pathog, 2015, 11(2): e1004643
CrossRef Google scholar
[221]
GimbroneMAJr., García-CardeñaG. Endothelial Cell Dysfunction and the Pathobiology of Atherosclerosis. Circ Res, 2016, 118(4): 620-636
CrossRef Google scholar
[222]
SawmaT, ShaitoA, NajmN, et al.. Role of RhoA and Rho-associated kinase in phenotypic switching of vascular smooth muscle cells: Implications for vascular function. Atherosclerosis, 2022, 358: 12-28
CrossRef Google scholar
[223]
MirallesF, PosernG, ZaromytidouAI, et al.. Actin dynamics control SRF activity by regulation of its coactivator MAL. Cell, 2003, 113(3): 329-342
CrossRef Google scholar
[224]
QiY, LiangX, DaiF, et al.. RhoA/ROCK Pathway Activation is Regulated by AT1 Receptor and Participates in Smooth Muscle Migration and Dedifferentiation via Promoting Actin Cytoskeleton Polymerization. Int J Mol Sci, 2020, 21(15): 5398
CrossRef Google scholar
[225]
KlocM, KubiakJZ, GhobrialRM. Macrophage-, Dendritic-, Smooth Muscle-, Endothelium-, and Stem Cells-Derived Foam Cells in Atherosclerosis. Int J Mol Sci, 2022, 23(22): 14154
CrossRef Google scholar
[226]
AllahverdianS, ChehroudiAC, McManusBM, et al.. Contribution of intimal smooth muscle cells to cholesterol accumulation and macrophage-like cells in human atherosclerosis. Circulation, 2014, 129(15): 1551-1559
CrossRef Google scholar
[227]
WangY, DublandJA, AllahverdianS, et al.. Smooth Muscle Cells Contribute the Majority of Foam Cells in ApoE (Apolipoprotein E)-Deficient Mouse Atherosclerosis. Arterioscler Thromb Vasc Biol, 2019, 39(5): 876-887
CrossRef Google scholar
[228]
DublandJA, FrancisGA. So Much Cholesterol: the unrecognized importance of smooth muscle cells in atherosclerotic foam cell formation. Curr Opin Lipidol, 2016, 27(2): 155-161
CrossRef Google scholar
[229]
CostalesP, Fuentes-PriorP, CastellanoJ, et al.. K Domain CR9 of Low Density Lipoprotein (LDL) Receptor-related Protein 1 (LRP1) Is Critical for Aggregated LDL-induced Foam Cell Formation from Human Vascular Smooth Muscle Cells. J Biol Chem, 2015, 290(24): 14852-14865
CrossRef Google scholar
[230]
YinYW, LiaoSQ, ZhangMJ, et al.. TLR4-mediated inflammation promotes foam cell formation of vascular smooth muscle cell by upregulating ACAT1 expression. Cell Death Dis, 2014, 5(12): e1574
CrossRef Google scholar
[231]
ChenZ, XueQ, CaoL, et al.. Toll-Like Receptor 4 Mediated Oxidized Low-Density Lipoprotein-Induced Foam Cell Formation in Vascular Smooth Muscle Cells via Src and Sirt1/3 Pathway. Mediators Inflamm, 2021, 2021: 6639252
CrossRef Google scholar
[232]
GabuniaK, HermanAB, RayM, et al.. Induction of MiR133a expression by IL-19 targets LDLRAP1 and reduces oxLDL uptake in VSMC. J Mol Cell Cardiol, 2017, 105: 38-48
CrossRef Google scholar
[233]
FanY, ZhangJ, ChenCY, et al.. Macrophage migration inhibitory factor triggers vascular smooth muscle cell dedifferentiation by a p68-serum response factor axis. Cardiovasc Res, 2017, 113(5): 519-530
CrossRef Google scholar
[234]
ShankmanLS, GomezD, CherepanovaOA, et al.. KLF4-dependent phenotypic modulation of smooth muscle cells has a key role in atherosclerotic plaque pathogenesis. Nat Med, 2015, 21(6): 628-637
CrossRef Google scholar
[235]
VendrovAE, SumidaA, CanugoviC, et al.. NOXA1-dependent NADPH oxidase regulates redox signaling and phenotype of vascular smooth muscle cell during atherogenesis. Redox Biol, 2019, 21: 101063
CrossRef Google scholar
[236]
WuJH, ZhangL, NepliouevI, et al.. Drebrin attenuates atherosclerosis by limiting smooth muscle cell transdifferentiation. Cardiovasc Res, 2022, 118(3): 772-784
CrossRef Google scholar
[237]
ChenC, WangY, YangS, et al.. MiR-320a contributes to atherogenesis by augmenting multiple risk factors and down-regulating SRF. J Cell Mol Med, 2015, 19(5): 970-985
CrossRef Google scholar
[238]
KarolinaDS, TavintharanS, ArmugamA, et al.. Circulating miRNA profiles in patients with metabolic syndrome. J Clin Endocrinol Metab, 2012, 97(12): E2271-E2276
CrossRef Google scholar
[239]
ZhangC, WangX. miR-320a Targeting RGS5 Aggravates Atherosclerosis by Promoting Migration and Proliferation of ox-LDL-Stimulated Vascular Smooth Muscle Cells. J Cardiovasc Pharmacol, 2022, 80(1): 110-117
CrossRef Google scholar
[240]
HakaAS, SinghRK, GroshevaI, et al.. Monocyte-Derived Dendritic Cells Upregulate Extracellular Catabolism of Aggregated Low-Density Lipoprotein on Maturation, Leading to Foam Cell Formation. Arterioscler Thromb Vasc Biol, 2015, 35(10): 2092-2103
CrossRef Google scholar
[241]
StellosK, SeizerP, BigalkeB, et al.. Platelet aggregates-induced human CD34+ progenitor cell proliferation and differentiation to macrophages and foam cells is mediated by stromal cell derived factor 1 in vitro.. Semin Thromb Hemost, 2010, 36(2): 139-145
CrossRef Google scholar
[242]
CorrêaR, SilvaLFF, RibeiroDJS, et al.. Lysophosphatidylcholine Induces NLRP3 Inflammasome-Mediated Foam Cell Formation and Pyroptosis in Human Monocytes and Endothelial Cells. Front Immunol, 2019, 10: 2927
CrossRef Google scholar
[243]
TadaY, YanoS, YamaguchiT, et al.. Advanced glycation end products-induced vascular calcification is mediated by oxidative stress: functional roles of NAD(P) H-oxidase. Horm Metab Res, 2013, 45(4): 267-272
[244]
GoettschC, RaunerM, HamannC, et al.. Nuclear factor of activated T cells mediates oxidised LDL-induced calcification of vascular smooth muscle cells. Diabetologia, 2011, 54(10): 2690-2701
CrossRef Google scholar
[245]
AlencarGF, OwsianyKM, KarnewarS, et al.. Stem Cell Pluripotency Genes Klf4 and Oct4 Regulate Complex SMC Phenotypic Changes Critical in Late-Stage Atherosclerotic Lesion Pathogenesis. Circulation, 2020, 142(21): 2045-2059
CrossRef Google scholar
[246]
ParhamiF, BasseriB, HwangJ, et al.. High-density lipoprotein regulates calcification of vascular cells. Circ Res, 2002, 91(7): 570-576
CrossRef Google scholar
[247]
FochiS, GiuriatoG, De SimoneT, et al.. Regulation of microRNAs in Satellite Cell Renewal, Muscle Function, Sarcopenia and the Role of Exercise. Int J Mol Sci, 2020, 21(18): 6732
CrossRef Google scholar
[248]
ShanahanCM, CrouthamelMH, KapustinA, et al.. Arterial calcification in chronic kidney disease: key roles for calcium and phosphate. Circ Res, 2011, 109(6): 697-711
CrossRef Google scholar
[249]
ZhangF, GuoX, XiaY, et al.. An update on the phenotypic switching of vascular smooth muscle cells in the pathogenesis of atherosclerosis. Cell Mol Life Sci, 2021, 79(1): 6
CrossRef Google scholar
[250]
ShroffRC, ShanahanCM. The vascular biology of calcification. Semin Dial, 2007, 20(2): 103-109
CrossRef Google scholar
[251]
BadiI, MancinelliL, PolizzottoA, et al.. miR-34a Promotes Vascular Smooth Muscle Cell Calcification by Downregulating SIRT1 (Sirturn 1) and Axl (AXL Receptor Tyrosine Kinase). Arterioscler Thromb Vasc Biol, 2018, 38(9): 2079-2090
CrossRef Google scholar
[252]
Di BartoloBA, SchoppetM, MattarMZ, et al.. Calcium and osteoprotegerin regulate IGF1R expression to inhibit vascular calcification. Cardiovasc Res, 2011, 91(3): 537-545
CrossRef Google scholar
[253]
KannoY, IntoT, LowensteinCJ, et al.. Nitric oxide regulates vascular calcification by interfering with TGF- signalling. Cardiovasc Res, 2008, 77(1): 221-230
CrossRef Google scholar
[254]
OhYJ, KimH, KimAJ, et al.. Reduction of Secreted Frizzled-Related Protein 5 Drives Vascular Calcification through Wnt3a-Mediated Rho/ROCK/JNK Signaling in Chronic Kidney Disease. Int J Mol Sci, 2020, 21(10): 3539
CrossRef Google scholar
[255]
NaikV, LeafEM, HuJH, et al.. Sources of cells that contribute to atherosclerotic intimal calcification: an in vivo genetic fate mapping study. Cardiovasc Res, 2012, 94(3): 545-554
CrossRef Google scholar
[256]
AlexopoulosN, RaggiP. Calcification in atherosclerosis. Nat Rev Cardiol, 2009, 6(11): 681-688
CrossRef Google scholar
[257]
HuangH, VirmaniR, YounisH, et al.. The impact of calcification on the biomechanical stability of atherosclerotic plaques. Circulation, 2001, 103(8): 1051-1056
CrossRef Google scholar
[258]
BeckmanJA, GanzJ, CreagerMA, et al.. Relationship of clinical presentation and calcification of culprit coronary artery stenoses. Arterioscler Thromb Vasc Biol, 2001, 21(10): 1618-1622
CrossRef Google scholar
[259]
MosseriM, SatlerLF, PichardAD, et al.. Impact of vessel calcification on outcomes after coronary stenting. Cardiovasc Revasc Med, 2005, 6(4): 147-153
CrossRef Google scholar
[260]
VenkitachalamL, MackeyRH, Sutton-TyrrellK, et al.. Elevated pulse wave velocity increases the odds of coronary calcification in overweight postmenopausal women. Am J Hypertens, 2007, 20(5): 469-475
CrossRef Google scholar
[261]
RamadanMM, MahfouzEM, GomaaGF, et al.. Evaluation of coronary calcium score by multidetector computed tomography in relation to endothelial function and inflammatory markers in asymptomatic individuals. Circ J, 2008, 72(5): 778-785
CrossRef Google scholar
[262]
EharaS, KobayashiY, YoshiyamaM, et al.. Spotty calcification typifies the culprit plaque in patients with acute myocardial infarction: an intravascular ultrasound study. Circulation, 2004, 110(22): 3424-3429
CrossRef Google scholar
[263]
MotoyamaS, KondoT, SaraiM, et al.. Multislice computed tomographic characteristics of coronary lesions in acute coronary syndromes. J Am Coll Cardiol, 2007, 50(4): 319-326
CrossRef Google scholar
[264]
WirkaRC, WaghD, PaikDT, et al.. Atheroprotective roles of smooth muscle cell phenotypic modulation and the TCF21 disease gene as revealed by single-cell analysis. Nat Med, 2019, 25(8): 1280-1289
CrossRef Google scholar
[265]
MillerCL, HaasU, DiazR, et al.. Coronary heart disease-associated variation in TCF21 disrupts a miR-224 binding site and miRNA-mediated regulation. PLoS Genet, 2014, 10(3): e1004263
CrossRef Google scholar
[266]
LeeHN, ChoiYY, KimJW, et al.. Effect of biochemical and biomechanical factors on vascularization of kidney organoid-on-a-chip. Nano Converg, 2021, 8(1): 35
CrossRef Google scholar
[267]
ChandaPK, MengS, LeeJ, et al.. Nuclear S-Nitrosylation Defines an Optimal Zone for Inducing Pluripotency. Circulation, 2019, 140(13): 1081-1099
CrossRef Google scholar
[268]
HongX, MargaritiA, Le BrasA, et al.. Transdifferentiated Human Vascular Smooth Muscle Cells are a New Potential Cell Source for Endothelial Regeneration. Sci Rep, 2017, 7(1): 5590
CrossRef Google scholar
[269]
GrootaertMOJ, BennettMR. Vascular smooth muscle cells in atherosclerosis: time for a re-assessment. Cardiovasc Res, 2021, 117(11): 2326-2339
CrossRef Google scholar
[270]
Nguyen Dinh CatA, BrionesAM, CalleraGE, et al.. Adipocyte-derived factors regulate vascular smooth muscle cells through mineralocorticoid and glucocorticoid receptors. Hypertension, 2011, 58(3): 479-488
CrossRef Google scholar
[271]
ChenPY, QinL, LiG, et al.. Smooth Muscle Cell Reprogramming in Aortic Aneurysms. Cell Stem Cell, 2020, 26(4): 542-557
CrossRef Google scholar
[272]
HergenreiderE, HeydtS, TréguerK, et al.. Atheroprotective communication between endothelial cells and smooth muscle cells through miRNAs. Nat Cell Biol, 2012, 14(3): 249-356
CrossRef Google scholar
[273]
DongK, ShenJ, HeX, et al.. CARMN Is an Evolutionarily Conserved Smooth Muscle Cell-Specific LncRNA That Maintains Contractile Phenotype by Binding Myocardin. Circulation, 2021, 144(23): 1856-1875
CrossRef Google scholar
[274]
HicksCW, DayaNR, BlackJH3rd, et al.. Race and sex-based disparities associated with carotid endarterectomy in the Atherosclerosis Risk in Communities (ARIC) study. Atherosclerosis, 2020, 292: 10-16
CrossRef Google scholar
[275]
SalemiS, PrangeJA, BaumgartnerV, et al.. Adult stem cell sources for skeletal and smooth muscle tissue engineering. Stem Cell Res Ther, 2022, 13(1): 156
CrossRef Google scholar
[276]
PittengerMF, MackayAM, BeckSC, et al.. Multilineage potential of adult human mesenchymal stem cells. Science, 1999, 284(5411): 143-147
CrossRef Google scholar
[277]
JiangY, JahagirdarBN, ReinhardtRL, et al.. Pluripotency of mesenchymal stem cells derived from adult marrow. Nature, 2002, 418(6893): 41-49
CrossRef Google scholar
[278]
HuangP, WangL, LiQ, et al.. Atorvastatin enhances the therapeutic efficacy of mesenchymal stem cells-derived exosomes in acute myocardial infarction via up-regulating long non-coding RNA H19. Cardiovasc Res, 2020, 116(2): 353-367
CrossRef Google scholar
[279]
XiongY, TangR, XuJ, et al.. Sequential transplantation of exosomes and mesenchymal stem cells pretreated with a combination of hypoxia and Tongxinluo efficiently facilitates cardiac repair. Stem Cell Res Ther, 2022, 13(1): 63
CrossRef Google scholar
[280]
NingY, HuangP, ChenG, et al.. Atorvastatin-pretreated mesenchymal stem cell-derived extracellular vesicles promote cardiac repair after myocardial infarction via shifting macrophage polarization by targeting microRNA-139-3p/Stat1 pathway. BMC Med, 2023, 21(1): 96
CrossRef Google scholar
[281]
GeorgeJ, AfekA, AbashidzeA, et al.. Transfer of endothelial progenitor and bone marrow cells influences atherosclerotic plaque size and composition in apolipoprotein E knockout mice. Arterioscler Thromb Vasc Biol, 2005, 25(12): 2636-2641
CrossRef Google scholar
[282]
TousoulisD, BriasoulisA, VogiatziG, et al.. Infusion of lin-/sca-1+ and endothelial progenitor cells improves proinflammatory and oxidative stress markers in atherosclerotic mice. Int J Cardiol, 2013, 167(5): 1900-1905
CrossRef Google scholar
[283]
WeiX, SunG, ZhaoX, et al.. Human amnion mesenchymal stem cells attenuate atherosclerosis by modulating macrophage function to reduce immune response. Int J Mol Med, 2019, 44(4): 1425-1435
[284]
LiQ, SunW, WangX, et al.. Skin-Derived Mesenchymal Stem Cells Alleviate Atherosclerosis via Modulating Macrophage Function. Stem Cells Transl Med, 2015, 4(11): 1294-1301
CrossRef Google scholar
[285]
WangSS, HuSW, ZhangQH, et al.. Mesenchymal Stem Cells Stabilize Atherosclerotic Vulnerable Plaque by Anti-Inflammatory Properties. PLoS One, 2015, 10(8): e0136026
CrossRef Google scholar
[286]
FrodermannV, van DuijnJ, van PelM, et al.. Mesenchymal Stem Cells Reduce Murine Atherosclerosis Development. Sci Rep, 2015, 5: 15559
CrossRef Google scholar
[287]
MuY, XuW, LiuJ, et al.. Mesenchymal stem cells moderate experimental autoimmune uveitis by dynamic regulating Th17 and Breg cells response. J Tissue Eng Regen Med, 2022, 16(1): 26-35
CrossRef Google scholar
[288]
ZhangX, HuangF, LiW, et al.. Human Gingiva-Derived Mesenchymal Stem Cells Modulate Monocytes/Macrophages and Alleviate Atherosclerosis. Front Immunol, 2018, 9: 878
CrossRef Google scholar
[289]
LiJZ, CaoTH, HanJC, et al.. Comparison of adipose- and bone marrow-derived stem cells in protecting against ox-LDL-induced inflammation in M1-macrophage-derived foam cells. Mol Med Rep, 2019, 19(4): 2660-2670
[290]
HongR, WangZ, SuiA, et al.. Gingival mesenchymal stem cells attenuate pro-inflammatory macrophages stimulated with oxidized low-density lipoprotein and modulate lipid metabolism. Arch Oral Biol, 2019, 98: 92-98
CrossRef Google scholar
[291]
SharmaM, SchlegelMP, AfonsoMS, et al.. Regulatory T Cells License Macrophage Pro-Resolving Functions During Atherosclerosis Regression. Circ Res, 2020, 127(3): 335-353
CrossRef Google scholar
[292]
FazioS, BabaevVR, MurrayAB, et al.. Increased atherosclerosis in mice reconstituted with apolipoprotein E null macrophages. Proc Natl Acad Sci USA, 1997, 94(9): 4647-4652
CrossRef Google scholar
[293]
Van EckM, HerijgersN, Vidgeon-HartM, et al.. Accelerated atherosclerosis in C57Bl/6 mice transplanted with ApoE-deficient bone marrow. Atherosclerosis, 2000, 150(1): 71-80
CrossRef Google scholar
[294]
YuB, ChenQ, Le BrasA, et al.. Vascular Stem/Progenitor Cell Migration and Differentiation in Atherosclerosis. Antioxid Redox Signal, 2018, 29(2): 219-235
CrossRef Google scholar
[295]
RauscherFM, Goldschmidt-ClermontPJ, DavisBH, et al.. Aging, progenitor cell exhaustion, and atherosclerosis. Circulation, 2003, 108(4): 457-463
CrossRef Google scholar
[296]
ZhangZ, LiZ, WangY, et al.. PDGF-BB/SA/Dex injectable hydrogels accelerate BMSC-mediated functional full thickness skin wound repair by promoting angiogenesis. J Mater Chem B, 2021, 9(31): 6176-6189
CrossRef Google scholar
[297]
LintonMF, AtkinsonJB, FazioS. Prevention of atherosclerosis in apolipoprotein E-deficient mice by bone marrow transplantation. Science, 1995, 267(5200): 1034-1037
CrossRef Google scholar
[298]
HerijgersN, Van EckM, GrootPH, et al.. Effect of bone marrow transplantation on lipoprotein metabolism and atherosclerosis in LDL receptor-knockout mice. Arterioscler Thromb Vasc Biol, 1997, 17(10): 1995-2003
CrossRef Google scholar
[299]
NelsonWD, ZenovichAG, OttHC, et al.. Sex-dependent attenuation of plaque growth after treatment with bone marrow mononuclear cells. Circ Res, 2007, 101(12): 1319-1327
CrossRef Google scholar
[300]
LiY, ShiG, HanY, et al.. Therapeutic potential of human umbilical cord mesenchymal stem cells on aortic atherosclerotic plaque in a high-fat diet rabbit model. Stem Cell Res Ther, 2021, 12(1): 407
CrossRef Google scholar
[301]
BromageDI, DavidsonSM, YellonDM. Stromal derived factor la: a chemokine that delivers a two-pronged defence of the myocardium. Pharmacol Ther, 2014, 143(3): 305-315
CrossRef Google scholar
[302]
LawsonC, WolfS. ICAM-1 signaling in endothelial cells. Pharmacol Rep, 2009, 61(1): 22-32
CrossRef Google scholar
[303]
MerckelbachS, van der VorstEPC, KallmayerM, et al.. Expression and Cellular Localization of CXCR4 and CXCL12 in Human Carotid Atherosclerotic Plaques. Thromb Haemost, 2018, 118(1): 195-206
CrossRef Google scholar
[304]
ChatterjeeM, von Ungern-SternbergSN, SeizerP, et al.. Platelet-derived CXCL12 regulates monocyte function, survival, differentiation into macrophages and foam cells through differential involvement of CXCR4-CXCR7. Cell Death Dis, 2015, 6(11): e1989
CrossRef Google scholar
[305]
NahrendorfM, JafferFA, KellyKA, et al.. Noninvasive vascular cell adhesion molecule-1 imaging identifies inflammatory activation of cells in atherosclerosis. Circulation, 2006, 114(14): 1504-1511
CrossRef Google scholar
[306]
HassanzadehA, ShamlouS, YousefiN, et al.. Genetically-modified Stem Cell in Regenerative Medicine and Cancer Therapy; A New Era. Curr Gene Ther, 2022, 22(1): 23-39
[307]
ChengG, WangX, LiY, et al.. Let-7a-transfected mesenchymal stem cells ameliorate monocrotaline-induced pulmonary hypertension by suppressing pulmonary artery smooth muscle cell growth through STAT3-BMPR2 signaling. Stem Cell Res Ther, 2017, 8(1): 34
CrossRef Google scholar
[308]
TaoX, SunM, ChenM, et al.. HMGB1-modified mesenchymal stem cells attenuate radiation-induced vascular injury possibly via their high motility and facilitation of endothelial differentiation. Stem Cell Res Ther, 2019, 10(1): 92
CrossRef Google scholar
[309]
TianXQ, YangYJ, LiQ, et al.. Combined therapy with atorvastatin and atorvastatin-pretreated mesenchymal stem cells enhances cardiac performance after acute myocardial infarction by activating SDF-1/CXCR4 axis. Am J Transl Res, 2019, 11(7): 4214-4231
[310]
Shafei AE, Ali MA, Ghanem HG, et al. Mesenchymal stem cell therapy: A promising cell-based therapy for treatment of myocardial infarction. J Gene Med, 2017,19(12). doi: https://doi.org/10.1002/jgm.2995
[311]
MaedaT, MandaiM, SugitaS, et al.. Strategies of pluripotent stem cell-based therapy for retinal degeneration: update and challenges. Trends Mol Med, 2022, 28(5): 388-404
CrossRef Google scholar
[312]
LinY, LiuM, ChenE, et al.. Bone marrow-derived mesenchymal stem cells microvesicles stabilize atherosclerotic plaques by inhibiting NLRP3-mediated macrophage pyroptosis. Cell Biol Int, 2021, 45(4): 820-830
CrossRef Google scholar
[313]
GaoH, YuZ, LiY, et al.. miR-100-5p in human umbilical cord mesenchymal stem cell-derived exosomes mediates eosinophilic inflammation to alleviate atherosclerosis via the FZD5/Wnt/β-catenin pathway. Acta Biochim Biophys Sin (Shanghai), 2021, 53(9): 1166-1176
CrossRef Google scholar
[314]
MaJ, ChenL, ZhuX, et al.. Mesenchymal stem cell-derived exosomal miR-21a-5p promotes M2 macrophage polarization and reduces macrophage infiltration to attenuate atherosclerosis. Acta Biochim Biophys Sin (Shanghai), 2021, 53(9): 1227-1236
CrossRef Google scholar
[315]
YangW, YinR, ZhuX, et al.. Mesenchymal stem-cell-derived exosomal miR-145 inhibits atherosclerosis by targeting JAM-A. Mol Ther Nucleic Acids, 2021, 23: 119-131
CrossRef Google scholar
[316]
XiaoX, XuM, YuH, et al.. Mesenchymal stem cell-derived small extracellular vesicles mitigate oxidative stress-induced senescence in endothelial cells via regulation of miR-146a/Src. Signal Transduct Target Ther, 2021, 6(1): 354
CrossRef Google scholar
[317]
Emini VeseliB, PerrottaP, De MeyerGRA, et al.. Animal models of atherosclerosis. Eur J Pharmacol, 2017, 816: 3-13
CrossRef Google scholar
[318]
PanQ, XuJ, WenCJ, et al.. Nanoparticles: Promising Tools for the Treatment and Prevention of Myocardial Infarction. Int J Nanomedicine, 2021, 16: 6719-6747
CrossRef Google scholar
[319]
PechanovaO, BartaA, KonerackaM, et al.. Protective Effects of Nanoparticle-Loaded Aliskiren on Cardiovascular System in Spontaneously Hypertensive Rats. Molecules, 2019, 24(15): 2710
CrossRef Google scholar
[320]
YuanLF, ShengJ, LuP, et al.. Nanoparticle-mediated RNA interference of angiotensinogen decreases blood pressure and improves myocardial remodeling in spontaneously hypertensive rats. Mol Med Rep, 2015, 12(3): 4657-4663
CrossRef Google scholar
[321]
Czyzynska-CichonI, Janik-HazukaM, Szafraniec-SzczęsnyJ, et al.. Low Dose Curcumin Administered in Hyaluronic Acid-Based Nanocapsules Induces Hypotensive Effect in Hypertensive Rats. Int J Nanomedicine, 2021, 16: 1377-1390
CrossRef Google scholar
[322]
Martín GiménezVM, Díaz-RodríguezP, SanzRL, et al.. Anandamide-nanoformulation obtained by electrospraying for cardiovascular therapy. Int J Pharm, 2019, 566: 1-10
CrossRef Google scholar
[323]
JinY, SongY, ZhuX, et al.. Goblet cell-targeting nanoparticles for oral insulin delivery and the influence of mucus on insulin transport. Biomaterials, 2012, 33(5): 1573-1582
CrossRef Google scholar
[324]
HasanAA, MadkorH, WagehS. Formulation and evaluation of metformin hydrochloride-loaded niosomes as controlled release drug delivery system. Drug Deliv, 2013, 20(3–4): 120-126
CrossRef Google scholar
[325]
MaoY, HuY, FengW, et al.. Effects and mechanisms of PSS-loaded nanoparticles on coronary microcirculation dysfunction in streptozotocin-induced diabetic cardio-myopathy rats. Biomed Pharmacother, 2020, 121: 109280
CrossRef Google scholar
[326]
ChenY, ZengY, ZhuX, et al.. Significant difference between sirolimus and paclitaxel nanoparticles in anti-proliferation effect in normoxia and hypoxia: The basis of better selection of atherosclerosis treatment. Bioact Mater, 2021, 6(3): 880-889
[327]
AhnS, LeeIH, LeeE, et al.. Oral delivery of an antidiabetic peptide drug via conjugation and complexation with low molecular weight chitosan. J Control Release, 2013, 170(2): 226-232
CrossRef Google scholar
[328]
BoadaC, ZingerA, TsaoC, et al.. Rapamycin-Loaded Biomimetic Nanoparticles Reverse Vascular Inflammation. Circ Res, 2020, 126(1): 25-37
CrossRef Google scholar
[329]
MaS, TianXY, ZhangY, et al.. E-selectin-targeting delivery of microRNAs by microparticles ameliorates endothelial inflammation and atherosclerosis. Sci Rep, 2016, 6: 22910
CrossRef Google scholar
[330]
SeijkensTTP, van TielCM, KustersPJH, et al.. Targeting CD40-Induced TRAF6 Signaling in Macrophages Reduces Atherosclerosis. J Am Coll Cardiol, 2018, 71(5): 527-542
CrossRef Google scholar
[331]
JiJ, YangJA, HeX, et al.. Cardiac-targeting transfection of tissue-type plasminogen activator gene to prevent the graft thrombosis and vascular anastomotic restenosis after coronary bypass. Thromb Res, 2014, 134(2): 440-448
CrossRef Google scholar
[332]
PanH, PalekarRU, HouKK, et al.. Anti-JNK2 peptide-siRNA nanostructures improve plaque endothelium and reduce thrombotic risk in atherosclerotic mice. Int J Nanomedicine, 2018, 13: 5187-5205
CrossRef Google scholar
[333]
SagerHB, DuttaP, DahlmanJE, et al.. RNAi targeting multiple cell adhesion molecules reduces immune cell recruitment and vascular inflammation after myocardial infarction. Sci Transl Med, 2016, 8(342): 342ra80
CrossRef Google scholar
[334]
Di FrancescoV, GurgoneD, PalombaR, et al.. Modulating Lipoprotein Transcellular Transport and Atherosclerotic Plaque Formation in ApoE(–/–) Mice via Nanoformulated Lipid-Methotrexate Conjugates. ACS Appl Mater Interfaces, 2020, 12(34): 37943-37956
CrossRef Google scholar
[335]
MishraS, BedjaD, AmuzieC, et al.. Improved intervention of atherosclerosis and cardiac hypertrophy through biodegradable polymer-encapsulated delivery of glycosphingolipid inhibitor. Biomaterials, 2015, 64: 125-135
CrossRef Google scholar
[336]
BarbieriLR, Lourenço-FilhoDD, TavaresER, et al.. Influence of Drugs Carried in Lipid Nanoparticles in Coronary Disease of Rabbit Transplanted Heart. Ann Thorac Surg, 2017, 104(2): 577-583
CrossRef Google scholar
[337]
GomesFLT, MaranhãoRC, TavaresER, et al.. Regression of Atherosclerotic Plaques of Cholesterol-Fed Rabbits by Combined Chemotherapy With Paclitaxel and Methotrexate Carried in Lipid Core Nanoparticles. J Cardiovasc Pharmacol Ther, 2018, 23(6): 561-569
CrossRef Google scholar
[338]
DaminelliEN, MartinelliAE, BulgarelliA, et al.. Reduction of Atherosclerotic Lesions by the Chemotherapeutic Agent Carmustine Associated to Lipid Nanoparticles. Cardiovasc Drugs Ther, 2016, 30(5): 433-443
CrossRef Google scholar
[339]
NingB, ChenY, WaqarAB, et al.. Hypertension Enhances Advanced Atherosclerosis and Induces Cardiac Death in Watanabe Heritable Hyperlipidemic Rabbits. Am J Pathol, 2018, 188(12): 2936-2947
CrossRef Google scholar
[340]
MairKM, RobinsonE, KaneKA, et al.. Interaction between anandamide and sphingosine-1-phosphate in mediating vasorelaxation in rat coronary artery. Br J Pharmacol, 2010, 161(1): 176-192
CrossRef Google scholar
[341]
WuZH, PingQN, WeiY, et al.. Hypoglycemic efficacy of chitosan-coated insulin liposomes after oral administration in mice. Acta Pharmacol Sin, 2004, 25(7): 966-972
[342]
García-DíazM, FogedC, NielsenHM. Improved insulin loading in poly(lactic-co-glycolic) acid (PLGA) nanoparticles upon self-assembly with lipids. Int J Pharm, 2015, 482(1–2): 84-91
CrossRef Google scholar
[343]
LuoXM, YanC, FengYM. Nanomedicine for the treatment of diabetes-associated cardiovascular diseases and fibrosis. Adv Drug Deliv Rev, 2021, 172: 234-248
CrossRef Google scholar
[344]
NakashiroS, MatobaT, UmezuR, et al.. Pioglitazone-Incorporated Nanoparticles Prevent Plaque Destabilization and Rupture by Regulating Monocyte/Macrophage Differentiation in ApoE–/–Mice. Arterioscler Thromb Vasc Biol, 2016, 36(3): 491-500
CrossRef Google scholar
[345]
AillonKL, XieY, El-GendyN, et al.. Effects of nanomaterial physicochemical properties on in vivo toxicity. Adv Drug Deliv Rev, 2009, 61(6): 457-466
CrossRef Google scholar
[346]
MarkovskyE, Baabur-CohenH, Eldar-BoockA, et al.. Administration, distribution, metabolism and elimination of polymer therapeutics. J Control Release, 2012, 161(2): 446-460
CrossRef Google scholar
[347]
FengL, YangX, LiangS, et al.. Silica nanoparticles trigger the vascular endothelial dysfunction and prethrombotic state via miR-451 directly regulating the IL6R signaling pathway. Part Fibre Toxicol, 2019, 16(1): 16
CrossRef Google scholar
[348]
DuanJ, YuY, YuY, et al.. Silica nanoparticles enhance autophagic activity, disturb endothelial cell homeostasis and impair angiogenesis. Part Fibre Toxicol, 2014, 11: 50
CrossRef Google scholar
[349]
DuanJ, LiangS, YuY, et al.. Inflammation-coagulation response and thrombotic effects induced by silica nanoparticles in zebrafish embryos. Nanotoxicology, 2018, 12(5): 470-484
CrossRef Google scholar
[350]
MaranhãoRC, GuidoMC, de LimaAD, et al.. Methotrexate carried in lipid core nanoparticles reduces myocardial infarction size and improves cardiac function in rats. Int J Nanomedicine, 2017, 12: 3767-3784
CrossRef Google scholar
[351]
DongZ, GuoJ, XingX, et al.. RGD modified and PEGylated lipid nanoparticles loaded with puerarin: Formulation, characterization and protective effects on acute myocardial ischemia model. Biomed Pharmacother, 2017, 89: 297-304
CrossRef Google scholar
[352]
NemmarA, BeegamS, YuvarajuP, et al.. Ultrasmall superparamagnetic iron oxide nanoparticles acutely promote thrombosis and cardiac oxidative stress and DNA damage in mice. Part Fibre Toxicol, 2016, 13(1): 22
CrossRef Google scholar
[353]
El-Hussainy elHM, HusseinAM, Abdel-AzizA, et al.. Effects of aluminum oxide (Al2O3) nanoparticles on ECG, myocardial inflammatory cytokines, redox state, and connexin 43 and lipid profile in rats: possible cardioprotective effect of gallic acid. Can J Physiol Pharmacol, 2016, 94(8): 868-878
CrossRef Google scholar
[354]
GuoB, YangF, ZhangL, et al.. Cuproptosis Induced by ROS Responsive Nanoparticles with Elesclomol and Copper Combined with aPD-Ll for Enhanced Cancer Immunotherapy. Adv Mater, 2023, 35(22): e2212267
CrossRef Google scholar
[355]
ChenW, LiD. Reactive Oxygen Species (ROS)-Responsive Nanomedicine for Solving Ischemia-Reperfusion Injury. Front Chem, 2020, 8: 732
CrossRef Google scholar
[356]
DengZ, LiuS. Inflammation-responsive delivery systems for the treatment of chronic inflammatory diseases. Drug Deliv Transl Res, 2021, 11(4): 1475-1497
CrossRef Google scholar
[357]
HuS, WangX, LiZ, et al.. Platelet membrane and stem cell exosome hybrid enhances cellular uptake and targeting to heart injury. Nano Today, 2021, 39: 101210
CrossRef Google scholar
[358]
LiangD, FengY, ZandkarimiF, et al.. Ferroptosis surveillance independent of GPX4 and differentially regulated by sex hormones. Cell, 2023, 86(13): 2748-2764.e22
CrossRef Google scholar
[359]
YalcinkayaM, FotakisP, LiuW, et al.. Cholesterol accumulation in macrophages drives NETosis in atherosclerotic plaques via IL-lβ secretion. Cardiovasc Res, 2023, 119(4): 969-981
CrossRef Google scholar
[360]
LibbyP. The changing landscape of atherosclerosis. Nature, 2021, 592(7855): 524-533
CrossRef Google scholar
[361]
van HasseltJGC, IyengarR. Systems Pharmacology: Defining the Interactions of Drug Combinations. Annu Rev Pharmacol Toxicol, 2019, 59: 21-40
CrossRef Google scholar
[362]
GuptaV, DattaP. Next-generation strategy for treating drug resistant bacteria: Antibiotic hybrids. Indian J Med Res, 2019, 149(2): 97-106
CrossRef Google scholar
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