Basic helix–loop–helix ARNT like 1 regulates the function of immune cells and participates in the development of immune-related diseases

Fanglin Shao , Zhipeng Wang , Luxia Ye , Ruicheng Wu , Jie Wang , Qing-Xin Yu , Dilinaer Wusiman , Zhouting Tuo , Koo Han Yoo , Ziyu Shu , Wuran Wei , Dengxiong Li , William C. Cho , Zhihong Liu , Dechao Feng

Burns & Trauma ›› 2025, Vol. 13 ›› Issue (1) : tkae075

PDF (1479KB)
Burns & Trauma ›› 2025, Vol. 13 ›› Issue (1) :tkae075 DOI: 10.1093/burnst/tkae075
Review
research-article
Basic helix–loop–helix ARNT like 1 regulates the function of immune cells and participates in the development of immune-related diseases
Author information +
History +
PDF (1479KB)

Abstract

The circadian clock is an internal timekeeper system that regulates biological processes through a central circadian clock and peripheral clocks controlling various genes. Basic helix–loop–helix ARNT-like 1 (BMAL1), also known as aryl hydrocarbon receptor nuclear translocator-like protein 1 (ARNTL1), is a key component of the circadian clock. The deletion of BMAL1 alone can abolish the circadian rhythms of the human body. BMAL1 plays a critical role in immune cell function. Dysregulation of BMAL1 is linked to immune-related diseases such as autoimmune diseases, infectious diseases, and cancer, and vice versa. This review highlights the significant role of BMAL1 in governing immune cells, including their development, differentiation, migration, homing, metabolism, and effector functions. This study also explores how dysregulation of BMAL1 can have far-reaching implications and potentially contribute to the onset of immune-related diseases such as autoimmune diseases, infectious diseases, cancer, sepsis, and trauma. Furthermore, this review discusses treatments for immune-related diseases that target BMAL1 disorders. Understanding the impact of BMAL1 on immune function can provide insights into the pathogenesis of immune-related diseases and help in the development of more effective treatment strategies. Targeting BMAL1 has been demonstrated to achieve good efficacy in immune-related diseases, indicating its promising potential as a targetable therapeutic target in these diseases.

Keywords

BMAL1 / ARNTL1 / Immune response / Autoimmune diseases / Infectious diseases / Cancer

Cite this article

Download citation ▾
Fanglin Shao, Zhipeng Wang, Luxia Ye, Ruicheng Wu, Jie Wang, Qing-Xin Yu, Dilinaer Wusiman, Zhouting Tuo, Koo Han Yoo, Ziyu Shu, Wuran Wei, Dengxiong Li, William C. Cho, Zhihong Liu, Dechao Feng. Basic helix–loop–helix ARNT like 1 regulates the function of immune cells and participates in the development of immune-related diseases. Burns & Trauma, 2025, 13 (1) : tkae075 DOI:10.1093/burnst/tkae075

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Patke A, Young MW, Axelrod S. Molecular mechanisms and physiological importance of circadian rhythms. Nat Rev Mol Cell Biol 2020; 21: 67-84. https://doi.org/10.1038/s41580-019-0179-2.

[2]

Zhang X, Pant SM, Ritch CC, Tang HY, Shao H, Dweep H, et al. Cell state dependent effects of Bmal1 on melanoma immunity and tumorigenicity. Nat Commun 2024; 15: 633. https://doi.org/10.1038/s41467-024-44778-2.

[3]

Liang C, Ke Q, Liu Z, Ren J, Zhang W, Hu J, et al. BMAL1 moonlighting as a gatekeeper for LINE1 repression and cellular senescence in primates. Nucleic Acids Res 2022; 50: 3323-47. https://doi.org/10.1093/nar/gkac146.

[4]

Zhou L, Zhang Z, Nice E, Huang C, Zhang W, Tang Y. Circadian rhythms and cancers: the intrinsic links and therapeutic potentials. J Hematol Oncol 2022; 15: 21. https://doi.org/10.1186/s13045-022-01238-y.

[5]

Xiang K, Xu Z, Hu YQ, He YS, Wu GC, Li TY, et al. Circadian clock genes as promising therapeutic targets for autoimmune diseases. Autoimmun Rev 2021; 20: 102866. https://doi.org/10.1016/j.autrev.2021.102866.

[6]

King DP, Takahashi JS. Molecular genetics of circadian rhythms in mammals. Annu Rev Neurosci 2000; 23: 713-42. https://doi.org/10.1146/annurev.neuro.23.1.713.

[7]

Reinke H, Asher G. Crosstalk between metabolism and circadian clocks. Nat Rev Mol Cell Biol 2019; 20: 227-41. https://doi.org/10.1038/s41580-018-0096-9.

[8]

Hood S, Amir S. The aging clock: circadian rhythms and later life. J Clin Invest 2017; 127: 437-46. https://doi.org/10.1172/JCI90328.

[9]

Fagiani F, Di Marino D, Romagnoli A, Travelli C, Voltan D, Di Cesare ML, et al. Molecular regulations of circadian rhythm and implications for physiology and diseases. Signal Transduct Target Ther 2022; 7: 41. https://doi.org/10.1038/s41392-022-00899-y.

[10]

Li E, Li X, Huang J, Xu C, Liang Q, Ren K, et al. BMAL1 regulates mitochondrial fission and mitophagy through mitochondrial protein BNIP3 and is critical in the development of dilated cardiomyopathy. Protein Cell 2020; 11: 661-79. https://doi.org/10.1007/s13238-020-00713-x.

[11]

Fortier EE, Rooney J, Dardente H, Hardy MP, Labrecque N, Cermakian N. Circadian variation of the response of T cells to antigen. J Immunol 2011; 187: 6291-300. https://doi.org/10.4049/jimmunol.1004030.

[12]

Xie M, Tang Q, Nie J, Zhang C, Zhou X, Yu S, et al. BMAL1-downregulation aggravates Porphyromonas gingivalis-induced atherosclerosis by encouraging oxidative stress. Circ Res 2020; 126: e15-29. https://doi.org/10.1161/CIRCRESAHA.119.315502.

[13]

Lavtar P, Rudolf G, Maver A, Hodžić A, Starčević Čizmarević N, Živković M, et al. Association of circadian rhythm genes ARNTL/BMAL1 and CLOCK with multiple sclerosis. PLoS One 2018; 13: e0190601. https://doi.org/10.1371/journal.pone.0190601.

[14]

Nguyen KD, Fentress SJ, Qiu Y, Yun K, Cox JS, Chawla A. Circadian gene Bmal1 regulates diurnal oscillations of Ly6C(hi) inflammatory monocytes. Science 2013; 341: 1483-8. https://doi.org/10.1126/science.1240636.

[15]

Halberg F, Johnson EA, Brown BW, Bittner JJ. Susceptibility rhythm to E. coli endotoxin and bioassay. Proc Soc Exp Biol Med 1960; 103: 142-4. https://doi.org/10.3181/00379727-103-25439.

[16]

Fernandes G, Halberg F, Yunis EJ, Good RA. Circadian rhythmic plaque-forming cell response of spleens from mice immunized with SRBC. J Immunol 1976; 117: 962-6. https://doi.org/10.4049/jimmunol.117.3.962.

[17]

Wyse C, O’Malley G, Coogan AN, McConkey S, Smith DJ. Seasonal and daytime variation in multiple immune parameters in humans: evidence from 329,261 participants of the UK biobank cohort. iScience 2021; 24: 102255. https://doi.org/10.1016/j.isci.2021.102255.

[18]

Timmons GA, O’Siorain JR, Kennedy OD, Curtis AM, Early JO. Innate rhythms: clocks at the center of monocyte and macrophage function. Front Immunol 2020; 11: 1743. https://doi.org/10.3389/fimmu.2020.01743.

[19]

Bollinger T, Leutz A, Leliavski A, Skrum L, Kovac J, Bonacina L, et al. Circadian clocks in mouse and human CD4+ T cells. PLoS One 2011; 6: e29801. https://doi.org/10.1371/journal.pone.0029801.

[20]

Cavadini G, Petrzilka S, Kohler P, Jud C, Tobler I, Birchler T, et al. TNF-alpha suppresses the expression of clock genes by interfering with E-box-mediated transcription. Proc Natl Acad Sci USA 2007; 104: 12843-8. https://doi.org/10.1073/pnas.0701466104.

[21]

Koyanagi S, Ohdo S. Alteration of intrinsic biological rhythms during interferon treatment and its possible mechanism. Mol Pharmacol 2002; 62: 1393-9. https://doi.org/10.1124/mol.62.6.1393.

[22]

Mackey SR.Biological rhythms workshop IA: molecular basis of rhythms generation. Cold Spring Harb Symp Quant Biol 2007; 72: 7-19. https://doi.org/10.1101/sqb.2007.72.060.

[23]

Bunger MK, Wilsbacher LD, Moran SM, Clendenin C, Radcliffe LA, Hogenesch JB, et al. Mop3 is an essential component of the master circadian pacemaker in mammals. Cell 2000; 103: 1009-17. https://doi.org/10.1016/S0092-8674(00)00205-1.

[24]

Hergenhan S, Holtkamp S, Scheiermann C. Molecular interactions between components of the circadian clock and the immune system. J Mol Biol 2020; 432: 3700-13. https://doi.org/10.1016/j.jmb.2019.12.044.

[25]

Spengler ML, Kuropatwinski KK, Comas M, Gasparian AV, Fedtsova N, Gleiberman AS, et al. Core circadian protein CLOCK is a positive regulator of NF-κB-mediated transcription. Proc Natl Acad Sci USA 2012; 109: E2457-65. https://doi.org/10.1073/pnas.1206274109.

[26]

Kawauchi T, Ishimaru K, Nakamura Y, Nakano N, Hara M, Ogawa H, et al. Clock-dependent temporal regulation of IL-33/ST2-mediated mast cell response. Allergol Int 2017; 66: 472-8. https://doi.org/10.1016/j.alit.2017.02.004.

[27]

Ando N, Nakamura Y, Aoki R, Ishimaru K, Ogawa H, Okumura K, et al. Circadian gene clock regulates psoriasis-like skin inflammation in mice. J Invest Dermatol 2015; 135: 3001-8. https://doi.org/10.1038/jid.2015.316.

[28]

Nader N, Chrousos GP, Kino T. Circadian rhythm transcription factor CLOCK regulates the transcriptional activity of the glucocorticoid receptor by acetylating its hinge region lysine cluster: potential physiological implications. FASEB J 2009; 23: 1572-83. https://doi.org/10.1096/fj.08-117697.

[29]

Voigt RM, Summa KC, Forsyth CB, Green SJ, Engen P, Naqib A, et al. The circadian clock mutation promotes intestinal dysbiosis. Alcohol Clin Exp Res 2016; 40: 335-47. https://doi.org/10.1111/acer.12943.

[30]

Narasimamurthy R, Hatori M, Nayak SK, Liu F, Panda S, Verma IM. Circadian clock protein cryptochrome regulates the expression of proinflammatory cytokines. Proc Natl Acad Sci USA 2012; 109: 12662-7. https://doi.org/10.1073/pnas.1209965109.

[31]

Chen K, Wang Y, Li D, Wu R, Wang J, Wei W, et al. Biological clock regulation by the PER gene family: a new perspective on tumor development. Front Cell Dev Biol 2024; 12: 1332506. https://doi.org/10.3389/fcell.2024.1332506.

[32]

Wang T, Wang Z, Yang P, Xia L, Zhou M, Wang S, et al. PER1 prevents excessive innate immune response during endotoxin-induced liver injury through regulation of macrophage recruitment in mice. Cell Death Dis 2016; 7: e2176. https://doi.org/10.1038/cddis.2016.9.

[33]

Ding Z, Ge W, Xu X, Xu X, Wang S, Zhang J. PER2/P65-driven glycogen synthase 1 transcription in macrophages modulates gut inflammation and pathogenesis of rectal prolapse. J Biol Chem 2023; 299: 105219. https://doi.org/10.1016/j.jbc.2023.105219.

[34]

Liu J, Malkani G, Shi X, Meyer M, Cunningham-Runddles S, Ma X, et al. The circadian clock period 2 gene regulates gamma interferon production of NK cells in host response to lipopolysaccharide-induced endotoxic shock. Infect Immun 2006; 74: 4750-6. https://doi.org/10.1128/IAI.00287-06.

[35]

Chen S, Fuller KK, Dunlap JC, Loros JJ. A pro-and anti-inflammatory axis modulates the macrophage circadian clock. Front Immunol 2020; 11: 867. https://doi.org/10.3389/fimmu.2020.00867.

[36]

Wang S, Lin Y, Yuan X, Li F, Guo L, Wu B. REV-ERBα integrates colon clock with experimental colitis through regulation of NF-κB/NLRP3 axis. Nat Commun 2018; 9: 4246. https://doi.org/10.1038/s41467-018-06568-5.

[37]

Pourcet B, Zecchin M, Ferri L, Beauchamp J, Sitaula S, Billon C, et al. Nuclear receptor subfamily 1 group D member 1 regulates circadian activity of NLRP3 inflammasome to reduce the severity of fulminant hepatitis in mice. Gastroenterology 2018; 154: 1449-64.e20. https://doi.org/10.1053/j.gastro.2017.12.019.

[38]

Dzhagalov I, Giguère V, He YW. Lymphocyte development and function in the absence of retinoic acid-related orphan receptor alpha. J Immunol 2004; 173: 2952-9. https://doi.org/10.4049/jimmunol.173.5.2952.

[39]

Shim DW, Eo JC, Kim S, Hwang I, Nam B, Shin JE, et al. Deficiency of circadian clock gene Bmal1 exacerbates noncanonical inflammasome-mediated pyroptosis and lethality via rev-erbα-C/EBPβ-SAA1 axis. Exp Mol Med 2024; 56: 370-82. https://doi.org/10.1038/s12276-024-01162-w.

[40]

Sun Y, Yang Z, Niu Z, Peng J, Li Q, Xiong W, et al. MOP3, a component of the molecular clock, regulates the development of B cells. Immunology 2006; 119: 451-60. https://doi.org/10.1111/j.1365-2567.2006.02456.x.

[41]

Hart AL, Ng SC, Mann E, Al-Hassi HO, Bernardo D, Knight SC. Homing of immune cells: role in homeostasis and intestinal inflammation. Inflamm Bowel Dis 2010; 16: 1969-77. https://doi.org/10.1002/ibd.21304.

[42]

Druzd D, Matveeva O, Ince L, Harrison U, He W, Schmal C, et al. Lymphocyte circadian clocks control lymph node trafficking and adaptive immune responses. Immunity 2017; 46: 120-32. https://doi.org/10.1016/j.immuni.2016.12.011.

[43]

Ella K, Csépányi-Kömi R, Káldi K. Circadian regulation of human peripheral neutrophils. Brain Behav Immun 2016; 57: 209-21. https://doi.org/10.1016/j.bbi.2016.04.016.

[44]

Cox SL, O’Siorain JR, He Y, Lordan R, Naik A, Tang SY, et al. Circadian disruption in lung fibroblasts enhances NF-κB activity to exacerbate neutrophil recruitment. FASEB J 2023; 37: e22753. https://doi.org/10.1096/fj.202201456R.

[45]

Adrover JM, Del Fresno C, Crainiciuc G, Cuartero MI, Casanova-Acebes M, Weiss LA, et al. A neutrophil timer coordinates immune defense and vascular protection. Immunity 2019; 50: 390-402.e10. https://doi.org/10.1016/j.immuni.2019.01.002.

[46]

Xu L, Yang TY, Zhou YW, Wu MF, Shen J, Cheng JL, et al. Bmal1 inhibits phenotypic transformation of hepatic stellate cells in liver fibrosis via IDH1/α-KG-mediated glycolysis. Acta Pharmacol Sin 2022; 43: 316-29. https://doi.org/10.1038/s41401-021-00658-9.

[47]

Zhou Y, Wu M, Xu L, Cheng J, Shen J, Yang T, et al. Bmal1 regulates macrophage polarize through glycolytic pathway in alcoholic liver disease. Front Pharmacol 2021; 12: 640521. https://doi.org/10.3389/fphar.2021.640521.

[48]

Deng W, Zhu S, Zeng L, Liu J, Kang R, Yang M, et al. The circadian clock controls immune checkpoint pathway in sepsis. Cell Rep 2018; 24: 366-78. https://doi.org/10.1016/j.celrep.2018.06.026.

[49]

Timmons GA, Carroll RG, O’Siorain JR, Cervantes-Silva MP, Fagan LE, Cox SL, et al. The circadian clock protein BMAL1 acts as a metabolic sensor in macrophages to control the production of pro IL-1β. Front Immunol 2021; 12: 700431. https://doi.org/10.3389/fimmu.2021.700431.

[50]

Alexander RK, Liou YH, Knudsen NH, Starost KA, Xu C, Hyde AL, et al. Bmal1 integrates mitochondrial metabolism and macrophage activation. elife 2020; 9: e54090. https://doi.org/10.7554/eLife.54090.

[51]

Ma Q. Role of nrf2 in oxidative stress and toxicity. Annu Rev Pharmacol Toxicol 2013; 53: 401-26. https://doi.org/10.1146/annurev-pharmtox-011112-140320.

[52]

Early JO, Menon D, Wyse CA, Cervantes-Silva MP, Zaslona Z, Carroll RG, et al. Circadian clock protein BMAL1 regulates IL-1β in macrophages via NRF2. Proc Natl Acad Sci USA 2018; 115: E8460-e8. https://doi.org/10.1073/pnas.1800431115.

[53]

Xu L, Liu Y, Cheng Q, Shen Y, Yuan Y, Jiang X, et al. Bmal1 downregulation worsens critical limb ischemia by promoting inflammation and impairing angiogenesis. Front Cardiovasc Med 2021; 8: 712903. https://doi.org/10.3389/fcvm.2021.712903.

[54]

Bellet MM, Zocchi L, Sassone-Corsi P. The RelB subunit of NFκB acts as a negative regulator of circadian gene expression. Cell Cycle 2012; 11: 3304-11. https://doi.org/10.4161/cc.21669.

[55]

Silver AC, Arjona A, Walker WE, Fikrig E. The circadian clock controls toll-like receptor 9-mediated innate and adaptive immunity. Immunity 2012; 36: 251-61. https://doi.org/10.1016/j.immuni.2011.12.017.

[56]

Kim E, Mawatari K, Yoo SH, Chen Z. The circadian Nobiletin-ROR axis suppresses adipogenic differentiation and IκBα/NF-κB signaling in adipocytes. Nutrients 2023; 15: 3919. https://doi.org/10.3390/nu15183919.

[57]

Xiao ZX, Miller JS, Zheng SG. An updated advance of autoantibodies in autoimmune diseases. Autoimmun Rev 2021; 20: 102743. https://doi.org/10.1016/j.autrev.2020.102743.

[58]

Radu AF, Bungau SG. Management of rheumatoid arthritis: an overview. Cells 2021; 10: 2857. https://doi.org/10.3390/cells10112857.

[59]

Xu Y, Wu Q. Prevalence trend and disparities in rheumatoid arthritis among US adults, 2005-2018. J Clin Med 2021; 10: 3289. https://doi.org/10.3390/jcm10153289.

[60]

Di Matteo A, Bathon JM, Emery P. Rheumatoid arthritis. Lancet 2023; 402: 2019-33. https://doi.org/10.1016/S0140-6736(23)01525-8.

[61]

Puttonen S, Oksanen T, Vahtera J, Pentti J, Virtanen M, Salo P, et al. Is shift work a risk factor for rheumatoid arthritis? The Finnish public sector study. Ann Rheum Dis 2010; 69: 679-80. https://doi.org/10.1136/ard.2008.099184.

[62]

Spies CM, Hoff P, Mazuch J, Gaber T, Maier B, Strehl C, et al. Circadian rhythms of cellular immunity in rheumatoid arthritis: a hypothesis-generating study. Clin Exp Rheumatol 2015; 33: 34-43.

[63]

Kaneshiro K, Nakagawa K, Tsukamoto H, Matsuoka G, Okuno S, Tateishi K, et al. The clock gene Bmal1 controls inflammatory mediators in rheumatoid arthritis fibroblast-like synoviocytes. Biochem Biophys Res Commun 2024; 691: 149315. https://doi.org/10.1016/j.bbrc.2023.149315.

[64]

Yoshida K, Nakai A, Kaneshiro K, Hashimoto N, Suzuki K, Uchida K, et al. TNF-α induces expression of the circadian clock gene Bmal1 via dual calcium-dependent pathways in rheumatoid synovial cells. Biochem Biophys Res Commun 2018; 495: 1675-80. https://doi.org/10.1016/j.bbrc.2017.12.015.

[65]

He X, Yu M, Zhao J, Wang A, Yin J, Wang H, et al. Chronomoxibustion adjusts circadian rhythm of CLOCK and BMAL1 in adjuvant-induced arthritic rats. Am J Transl Res 2022; 14: 4880-97.

[66]

Jahanban-Esfahlan R, Mehrzadi S, Reiter RJ, Seidi K, Majidinia M, Baghi HB, et al. Melatonin in regulation of inflammatory pathways in rheumatoid arthritis and osteoarthritis: involvement of circadian clock genes. Br J Pharmacol 2018; 175: 3230-8. https://doi.org/10.1111/bph.13898.

[67]

Dobson R, Giovannoni G. Multiple sclerosis-a review. Eur J Neurol 2019; 26: 27-40. https://doi.org/10.1111/ene.13819.

[68]

Sutton CE, Finlay CM, Raverdeau M, Early JO, DeCourcey J, Zaslona Z, et al. Loss of the molecular clock in myeloid cells exacerbates T cell-mediated CNS autoimmune disease. Nat Commun 2017; 8: 1923. https://doi.org/10.1038/s41467-017-02111-0.

[69]

Richards J, Diaz AN, Gumz ML. Clock genes in hypertension: novel insights from rodent models. Blood Press Monit 2014; 19: 249-54. https://doi.org/10.1097/MBP.0000000000000060.

[70]

Rojo D, Dal Cengio L, Badner A, Kim S, Sakai N, Greene J, et al. BMAL1 loss in oligodendroglia contributes to abnormal myelination and sleep. Neuron 2023; 111: 3604-18.e11. https://doi.org/10.1016/j.neuron.2023.08.002.

[71]

Nagy AD, Iwamoto A, Kawai M, Goda R, Matsuo H, Otsuka T, et al. Melatonin adjusts the expression pattern of clock genes in the suprachiasmatic nucleus and induces antidepressant-like effect in a mouse model of seasonal affective disorder. Chronobiol Int 2015; 32: 447-57. https://doi.org/10.3109/07420528.2014.992525.

[72]

de Rojas I, Martin-Montero C, Fedetz M, González-Jiménez A, Matesanz F, Urcelay E, et al. Polymorphisms in ARNTL/BMAL1 and CLOCK are not associated with multiple sclerosis in Spanish population. Biology (Basel) 2022; 11: 1417. https://doi.org/10.3390/biology11101417.

[73]

Redondo MJ, Morgan NG. Heterogeneity and endotypes in type 1 diabetes mellitus. Nat Rev Endocrinol 2023; 19: 542-54. https://doi.org/10.1038/s41574-023-00853-0.

[74]

Lebailly B, Boitard C, Rogner UC. Circadian rhythm-related genes: implication in autoimmunity and type 1 diabetes. Diabetes Obes Metab 2015; 17 Suppl 1: 134-8. https://doi.org/10.1111/dom.12525.

[75]

Song F, Xue Y, Dong D, Liu J, Fu T, Xiao C, et al. Insulin restores an altered corneal epithelium circadian rhythm in mice with streptozotocin-induced type 1 diabetes. Sci Rep 2016; 6: 32871. https://doi.org/10.1038/srep32871.

[76]

Vargas-Uricoechea H. Molecular mechanisms in autoimmune thyroid disease. Cells 2023; 12: 918. https://doi.org/10.3390/cells12060918.

[77]

Fu J, Fan Z, He L, Liu Q, Liu H, Li Y, et al. Circadian clock disruption in autoimmune thyroiditis. Eur Thyroid J 2023; 12.

[78]

Kahaly GJ, Frommer L. Polyglandular autoimmune syndromes. J Endocrinol Investig 2018; 41: 91-8. https://doi.org/10.1007/s40618-017-0740-9.

[79]

Angelousi A, Nasiri-Ansari N, Spilioti E, Mantzou E, Kalotyxou V, Chrousos G, et al. Altered expression of circadian clock genes in polyglandular autoimmune syndrome type III. Endocrine 2018; 59: 109-19. https://doi.org/10.1007/s12020-017-1407-1.

[80]

Muratori L, Lohse AW, Lenzi M. Diagnosis and management of autoimmune hepatitis. BMJ 2023; 380: e070201. https://doi.org/10.1136/bmj-2022-070201.

[81]

Liu Z, Zhang J, Li S, Wang H, Ren B, Li J, et al. Circadian control of ConA-induced acute liver injury and inflammatory response via Bmal1 regulation of Junb. JHEP Rep 2023; 5: 100856. https://doi.org/10.1016/j.jhepr.2023.100856.

[82]

Kitchen GB, Cunningham PS, Poolman TM, Iqbal M, Maidstone R, Baxter M, et al. The clock gene Bmal1 inhibits macrophage motility, phagocytosis, and impairs defense against pneumonia. Proc Natl Acad Sci USA 2020; 117: 1543-51. https://doi.org/10.1073/pnas.1915932117.

[83]

Majumdar T, Dhar J, Patel S, Kondratov R, Barik S. Circadian transcription factor BMAL1 regulates innate immunity against select RNA viruses. Innate Immun 2017; 23: 147-54. https://doi.org/10.1177/1753425916681075.

[84]

Edgar RS, Stangherlin A, Nagy AD, Nicoll MP, Efstathiou S, O’Neill JS, et al. Cell autonomous regulation of herpes and influenza virus infection by the circadian clock. Proc Natl Acad Sci USA 2016; 113: 10085-90. https://doi.org/10.1073/pnas.1601895113.

[85]

Kirchner SJ, Lei V, Kim PT, Patel M, Shannon JL, Corcoran D, et al. An aging-susceptible circadian rhythm controls cutaneous antiviral immunity. JCI Insight 2023; 8: e171548. https://doi.org/10.1172/jci.insight.171548.

[86]

Ehlers A, Xie W, Agapov E, Brown S, Steinberg D, Tidwell R, et al. BMAL1 links the circadian clock to viral airway pathology and asthma phenotypes. Mucosal Immunol 2018; 11: 97-111. https://doi.org/10.1038/mi.2017.24.

[87]

Zhuang X, Tsukuda S, Wrensch F, Wing PAC, Schilling M, Harris JM, et al. The circadian clock component BMAL1 regulates SARS-CoV-2 entry and replication in lung epithelial cells. iScience 2021; 24: 103144. https://doi.org/10.1016/j.isci.2021.103144.

[88]

Zhuang X, Forde D, Tsukuda S, D’Arienzo V, Mailly L, Harris JM, et al. Circadian control of hepatitis B virus replication. Nat Commun 2021; 12: 1658. https://doi.org/10.1038/s41467-021-21821-0.

[89]

Zhuang X, Magri A, Hill M, Lai AG, Kumar A, Rambhatla SB, et al. The circadian clock components BMAL1 and REV-ERBα regulate flavivirus replication. Nat Commun 2019; 10: 377. https://doi.org/10.1038/s41467-019-08299-7.

[90]

Chang CC, Naranbhai V, Stern J, Roche M, Dantanarayana A, Ke R, et al. Variation in cell-associated unspliced HIV RNA on antiretroviral therapy is associated with the circadian regulator brain-and-muscle-ARNT-like-1. AIDS 2018; 32: 2119-28. https://doi.org/10.1097/QAD.0000000000001937.

[91]

Li T, Shao W, Li S, Ma L, Zheng L, Shang W, et al. H. pylori infection induced BMAL1 expression and rhythm disorder aggravate gastric inflammation. EBioMedicine 2019; 39: 301-14. https://doi.org/10.1016/j.ebiom.2018.11.043.

[92]

Sulli G, Lam MTY, Panda S. Interplay between circadian clock and cancer: new frontiers for cancer treatment. Trends Cancer 2019; 5: 475-94. https://doi.org/10.1016/j.trecan.2019.07.002.

[93]

Straif K, Baan R, Grosse Y, Secretan B, El Ghissassi F, Bouvard V, et al. Carcinogenicity of shift-work, painting, and fire-fighting. Lancet Oncol 2007; 8: 1065-6. https://doi.org/10.1016/S1470-2045(07)70373-X.

[94]

de Assis LVM, Kinker GS, Moraes MN, Markus RP, Fernandes PA, Castrucci AML. Expression of the circadian clock gene BMAL1 positively correlates with antitumor immunity and patient survival in metastatic melanoma. Front Oncol 2018; 8: 185. https://doi.org/10.3389/fonc.2018.00185.

[95]

Pereira MA, Pertille Ramos MFK, Dias AR, Cardili L, de Moraes RDR, Ribeiro RRE, et al. Prognostic implications of tumor-infiltrating lymphocytes in association with programmed cell death ligand 1 expression in remnant gastric cancer. Chin J Cancer Res 2022; 34: 612-22. https://doi.org/10.21147/j.issn.1000-9604.2022.06.09.

[96]

Pei B, Ma X, Wu N, Wang C, Yang W. Effect of microbiome group on immune checkpoint inhibitors in treatment of gastrointestinal tumors. Chin J Cancer Res 2023; 35: 252-65. https://doi.org/10.21147/j.issn.1000-9604.2023.03.05.

[97]

Chen P, Hsu WH, Chang A, Tan Z, Lan Z, Zhou A, et al. Circadian regulator CLOCK recruits immune-suppressive microglia into the GBM tumor microenvironment. Cancer Discov 2020; 10: 371-81. https://doi.org/10.1158/2159-8290.CD-19-0400.

[98]

Xuan W, Hsu WH, Khan F, Dunterman M, Pang L, Wainwright DA, et al. Circadian regulator CLOCK drives immunosuppression in glioblastoma. Cancer Immunol Res 2022; 10: 770-84. https://doi.org/10.1158/2326-6066.CIR-21-0559.

[99]

Pang K, Shi ZD, Wei LY, Dong Y, Ma YY, Wang W, et al. Research progress of therapeutic effects and drug resistance of immunotherapy based on PD-1/PD-L1 blockade. Drug Resist Updat 2023; 66: 100907. https://doi.org/10.1016/j.drup.2022.100907.

[100]

Zhu P, Li SY, Ding J, Fei Z, Sun SN, Zheng ZH, et al. Combination immunotherapy of glioblastoma with dendritic cell cancer vaccines, anti-PD-1 and poly I:C. J Pharm Anal 2023; 13: 616-24. https://doi.org/10.1016/j.jpha.2023.04.012.

[101]

Yeh CM, Shay J, Zeng TC, Chou JL, Huang TH, Lai HC, et al. Epigenetic silencing of ARNTL, a circadian gene and potential tumor suppressor in ovarian cancer. Int J Oncol 2014; 45: 2101-7. https://doi.org/10.3892/ijo.2014.2627.

[102]

Kuo SJ, Chen ST, Yeh KT, Hou MF, Chang YS, Hsu NC, et al. Disturbance of circadian gene expression in breast cancer. Virchows Arch 2009; 454: 467-74. https://doi.org/10.1007/s00428-009-0761-7.

[103]

Kwon YJ, Seo EB, Kwon SH, Lee SH, Kim SK, Park SK, et al. Extracellular acidosis promotes metastatic potency via decrease of the BMAL1 circadian clock gene in breast cancer. Cells 2020; 9: 989. https://doi.org/10.3390/cells9040989.

[104]

Korkmaz T, Aygenli F, Emisoglu H, Ozcelik G, Canturk A, Yilmaz S, et al. Opposite carcinogenic effects of circadian clock gene BMAL1. Sci Rep 2018; 8: 16023. https://doi.org/10.1038/s41598-018-34433-4.

[105]

Saeed H, Leibowitz BJ, Zhang L, Yu J. Targeting Myc-driven stress addiction in colorectal cancer. Drug Resist Updat 2023; 69: 100963. https://doi.org/10.1016/j.drup.2023.100963.

[106]

Papagiannakopoulos T, Bauer MR, Davidson SM, Heimann M, Subbaraj L, Bhutkar A, et al. Circadian rhythm disruption promotes lung tumorigenesis. Cell Metab 2016; 24: 324-31. https://doi.org/10.1016/j.cmet.2016.07.001.

[107]

Bu Y, Yoshida A, Chitnis N, Altman BJ, Tameire F, Oran A, et al. A PERK-miR-211 axis suppresses circadian regulators and protein synthesis to promote cancer cell survival. Nat Cell Biol 2018; 20: 104-15. https://doi.org/10.1038/s41556-017-0006-y.

[108]

Taniguchi H, Fernández AF, Setién F, Ropero S, Ballestar E, Villanueva A, et al. Epigenetic inactivation of the circadian clock gene BMAL1 in hematologic malignancies. Cancer Res 2009; 69: 8447-54. https://doi.org/10.1158/0008-5472.CAN-09-0551.

[109]

Abreu M, Basti A, Genov N, Mazzoccoli G, Relógio A. The reciprocal interplay between TNFα and the circadian clock impacts on cell proliferation and migration in Hodgkin lymphoma cells. Sci Rep 2018; 8: 11474. https://doi.org/10.1038/s41598-018-29847-z.

[110]

Tang Q, Cheng B, Xie M, Chen Y, Zhao J, Zhou X, et al. Circadian clock gene Bmal1 inhibits tumorigenesis and increases paclitaxel sensitivity in tongue squamous cell carcinoma. Cancer Res 2017; 77: 532-44. https://doi.org/10.1158/0008-5472.CAN-16-1322.

[111]

Zeng ZL, Luo HY, Yang J, Wu WJ, Chen DL, Huang P, et al. Overexpression of the circadian clock gene Bmal1 increases sensitivity to oxaliplatin in colorectal cancer. Clin Cancer Res 2014; 20: 1042-52. https://doi.org/10.1158/1078-0432.CCR-13-0171.

[112]

Yoon J, Kym D, Hur J, Park J, Kim M, Cho YS, et al. The clinical differentiation of blood culture-positive and-negative sepsis in burn patients: a retrospective cohort study. Burns Trauma 2023; 11: tkad031. https://doi.org/10.1093/burnst/tkad031.

[113]

Geiger SS, Traba J, Richoz N, Farley TK, Brooks SR, Petermann F, et al. Feeding-induced resistance to acute lethal sepsis is dependent on hepatic BMAL1 and FXR signalling. Nat Commun 2021; 12: 2745. https://doi.org/10.1038/s41467-021-22961-z.

[114]

Lin H, Ji F, Lin KQ, Zhu YT, Yang W, Zhang LH, et al. LPS-aggravated ferroptosis via disrupting circadian rhythm by Bmal1/AKT/p53 in sepsis-induced myocardial injury. Inflammation 2023; 46: 1133-43. https://doi.org/10.1007/s10753-023-01804-7.

[115]

Zeng T, Liang L, Deng W, Xie M, Zhao M, Wang S, et al. BMAL1 plays a crucial role in immune homeostasis during sepsis-induced acute lung injury. Biochem Pharmacol 2024; 226: 116379. https://doi.org/10.1016/j.bcp.2024.116379.

[116]

Zhao ZA, Yan L, Wen J, Satyanarayanan SK, Yu F, Lu J, et al. Cellular and molecular mechanisms in vascular repair after traumatic brain injury: a narrative review. Burns Trauma 2023; 11: tkad033. https://doi.org/10.1093/burnst/tkad033.

[117]

Korthas HT, Main BS, Harvey AC, Buenaventura RG, Wicker E, Forcelli PA, et al. The effect of traumatic brain injury on sleep architecture and circadian rhythms in mice-a comparison of high-frequency head impact and controlled cortical injury. Biology (Basel) 2022; 11: 11. https://doi.org/10.3390/biology11071031.

[118]

Zhanfeng N, Hechun X, Zhijun Z, Hongyu X, Zhou F. Regulation of circadian clock genes on sleep disorders in traumatic brain injury patients. World Neurosurg 2019; 130: e475-86. https://doi.org/10.1016/j.wneu.2019.06.122.

[119]

Kuo LT, Lu HY, Chen YH. Traumatic brain injury-induced disruption of the circadian clock. J Mol Med (Berl) 2024; 102: 403-14. https://doi.org/10.1007/s00109-024-02416-w.

[120]

Li B, Li D, Ni H, Liu C, Xiong J, Liu H, et al. The circadian clock regulator Bmal1 affects traumatic brain injury in rats through the p38 MAPK signalling pathway. Brain Res Bull 2022; 178: 17-28. https://doi.org/10.1016/j.brainresbull.2021.11.003.

[121]

Kroetsch JT, Lidington D, Alibhai FJ, Reitz CJ, Zhang H, Dinh DD, et al. Disrupting circadian control of peripheral myogenic reactivity mitigates cardiac injury following myocardial infarction. Cardiovasc Res 2023; 119: 1403-15. https://doi.org/10.1093/cvr/cvac174.

[122]

Slomnicki LP, Myers SA, Saraswat Ohri S, Parsh MV, Andres KR, Chariker JH, et al. Improved locomotor recovery after contusive spinal cord injury in Bmal1(−/−) mice is associated with protection of the blood spinal cord barrier. Sci Rep 2020; 10: 14212. https://doi.org/10.1038/s41598-020-71131-6.

[123]

Tani N, Ikeda T, Aoki Y, Shida A, Oritani S, Ishikawa T. Pathophysiological significance of clock genes BMAL1 and PER2 as erythropoietin-controlling factors in acute blood hemorrhage. Hum Cell 2019; 32: 275-84. https://doi.org/10.1007/s13577-019-00248-2.

[124]

Dakup PP, Porter KI, Gaddameedhi S. The circadian clock protects against acute radiation-induced dermatitis. Toxicol Appl Pharmacol 2020; 399: 115040. https://doi.org/10.1016/j.taap.2020.115040.

[125]

Dakup PP, Porter KI, Gajula RP, Goel PN, Cheng Z, Gaddameedhi S. The circadian clock protects against ionizing radiation-induced cardiotoxicity. FASEB J 2020; 34: 3347-58. https://doi.org/10.1096/fj.201901850RR.

[126]

Alekya T, Narendar D, Mahipal D, Arjun N, Nagaraj B. Design and evaluation of chronomodulated drug delivery of tramadol hydrochloride. Drug Res (Stuttg) 2018; 68: 174-80. https://doi.org/10.1055/s-0043-119072.

[127]

Wang F, Liao W, Li C, Zhu L. Silencing BMAL1 promotes M1/M2 polarization through the LDHA/lactate axis to promote GBM sensitivity to bevacizumab. Int Immunopharmacol 2024; 134: 112187. https://doi.org/10.1016/j.intimp.2024.112187.

[128]

Wang J, Huang Q, Hu X, Zhang S, Jiang Y, Yao G, et al. Disrupting circadian rhythm via the PER1-HK2 axis reverses trastuzumab resistance in gastric cancer. Cancer Res 2022; 82: 1503-17. https://doi.org/10.1158/0008-5472.CAN-21-1820.

[129]

Teixeira AAS, Biondo LA, Silveira LS, Lima EA, Batatinha HA, Diniz TA, et al. Doxorubicin modulated clock genes and cytokines in macrophages extracted from tumor-bearing mice. Cancer Biol Ther 2020; 21: 344-53. https://doi.org/10.1080/15384047.2019.1702400.

[130]

Feng D, Xiao Y, Wang J, Wu R, Tuo Z, Yoo KH, et al. Unraveling links between aging, circadian rhythm and cancer: insights from evidence-based analysis. Chin J Cancer Res 2024; 36: 341-50.

[131]

Pawelec G.Age and immunity: what is "immunosenescence"? Exp Gerontol 2018; 105: 4-9. https://doi.org/10.1016/j.exger.2017.10.024.

[132]

Shen W, He J, Hou T, Si J, Chen S. Common pathogenetic mechanisms underlying aging and tumor and means of interventions. Aging Dis 2022; 13: 1063-91. https://doi.org/10.14336/AD.2021.1208.

[133]

Yu J, Li T, Zhu J. Gene therapy strategies targeting aging-related diseases. Aging Dis 2023; 14: 398-417. https://doi.org/10.14336/AD.2022.00725.

[134]

Li D, Yu Q, Wu R, Tuo Z, Wang J, Ye L, et al. Interactions between oxidative stress and senescence in cancer: mechanisms, therapeutic implications, and future perspectives. Redox Biol 2024; 73: 103208. https://doi.org/10.1016/j.redox.2024.103208.

[135]

Martinez-Ruiz L, Florido J, Rodriguez-Santana C, López-Rodríguez A, Guerra-Librero A, Fernández-Gil BI, et al. Intratumoral injection of melatonin enhances tumor regression in cell line-derived and patient-derived xenografts of head and neck cancer by increasing mitochondrial oxidative stress. Biomed Pharmacother 2023; 167: 115518. https://doi.org/10.1016/j.biopha.2023.115518.

[136]

Feng DC, Zhu WZ, Wang J, Li DX, Shi X, Xiong Q, et al. The implications of single-cell RNA-seq analysis in prostate cancer: unraveling tumor heterogeneity, therapeutic implications and pathways towards personalized therapy. Mil Med Res 2024; 11: 21. https://doi.org/10.1186/s40779-024-00526-7.

[137]

An Z, Liu W, Li W, Wei M, An C, et al. Application of single-cell RNA sequencing in head and neck squamous cell carcinoma. Chin J Cancer Res 2023; 35: 331-42. https://doi.org/10.21147/j.issn.1000-9604.2023.04.01.

[138]

Zhou B, Guo W, Guo L, Li Y, Zheng Z, Huai Q, et al. Single-cell RNA-sequencing data reveals the genetic source of extracellular vesicles in esophageal squamous cell carcinoma. Pharmacol Res 2023; 192: 106800. https://doi.org/10.1016/j.phrs.2023.106800.

[139]

He L, Fan Y, Zhang Y, Tu T, Zhang Q, Yuan F, et al. Single-cell transcriptomic analysis reveals circadian rhythm disruption associated with poor prognosis and drug-resistance in lung adenocarcinoma. J Pineal Res 2022; 73: e12803. https://doi.org/10.1111/jpi.12803.

[140]

Wang G, Mao X, Wang W, Wang X, Li S, Wang Z. Bioprinted research models of urological malignancy. Exploration 2024; 4: 2023126. https://doi.org/10.1002/EXP.20230126.

[141]

Zienolddiny S, Haugen A, Lie JA, Kjuus H, Anmarkrud KH, Kjærheim K. Analysis of polymorphisms in the circadian-related genes and breast cancer risk in Norwegian nurses working night shifts. Breast Cancer Res 2013; 15: R53. https://doi.org/10.1186/bcr3445.

[142]

Xiao T, Dong X, Lu Y, Zhou W. High-resolution and multidimensional phenotypes can complement genomics data to diagnose diseases in the neonatal population. Phenomics 2023; 3: 204-15. https://doi.org/10.1007/s43657-022-00071-0.

[143]

Wei J, Montalvo-Ortiz W, Yu L, Krasco A, Ebstein S, Cortez C, et al. Sequence of αPD-1 relative to local tumor irradiation determines the induction of abscopal antitumor immune responses. Sci Immunol 2021; 6: eabg0117. https://doi.org/10.1126/sciimmunol.abg0117.

[144]

Stump CT, Roehle K, Manjarrez Orduno N, Dougan SK. Radiation combines with immune checkpoint blockade to enhance T cell priming in a murine model of poorly immunogenic pancreatic cancer. Open Biol 2021; 11: 210245. https://doi.org/10.1098/rsob.210245.

[145]

Patrizia G, Ilaria P, Orazio F, Francesca P. Immunomodulatory role of EV-derived non-coding RNA in lung cancer. Extracell Vesicles Circ Nucl Acids 2023; 4: 44-56. https://doi.org/10.20517/evcna.2022.42.

[146]

Xia Y, Zhang J. Leveraging biomimetic synthesis strategy for next-generation dendritic cell nanovaccines. Extracell Vesicles Circ Nucl Acids 2022; 3: 301-5. https://doi.org/10.20517/evcna.2022.35.

[147]

Butler CT, Rodgers AM, Curtis AM, Donnelly RF. Chrono-tailored drug delivery systems: recent advances and future directions. Drug Deliv Transl Res 2024; 14: 1756-75. https://doi.org/10.1007/s13346-024-01539-4.

[148]

Weng T, Wang J, Yang M, Zhang W, Wu P, You C, et al. Nanomaterials for the delivery of bioactive factors to enhance angiogenesis of dermal substitutes during wound healing. Burns Trauma 2022; 10: tkab049. https://doi.org/10.1093/burnst/tkab049.

[149]

Johnson RP, Ratnacaram CK, Kumar L, Jose J. Combinatorial approaches of nanotherapeutics for inflammatory pathway targeted therapy of prostate cancer. Drug Resist Updat 2022; 64: 100865. https://doi.org/10.1016/j.drup.2022.100865.

[150]

Li J, Zhu L, Kwok HF. Nanotechnology-based approaches overcome lung cancer drug resistance through diagnosis and treatment. Drug Resist Updat 2023; 66: 100904. https://doi.org/10.1016/j.drup.2022.100904.

[151]

Xue X, Qu H, Li Y. Stimuli-responsive crosslinked nanomedicine for cancer treatment. Exploration (Beijing) 2022; 2: 20210134. https://doi.org/10.1002/EXP.20210134.

[152]

Kubiatowicz LJ, Mohapatra A, Krishnan N, Fang RH, Zhang L. mRNA nanomedicine: design and recent applications. Exploration (Beijing) 2022; 2: 20210217. https://doi.org/10.1002/EXP.20210217.

[153]

Yao L, Bojic D, Liu M. Applications and safety of gold nanoparticles as therapeutic devices in clinical trials. J Pharm Anal 2023; 13: 960-7. https://doi.org/10.1016/j.jpha.2023.06.001.

[154]

Chen B, Guo K, Zhao X, Liu Z, Xu C, Zhao N, et al. Tumor microenvironment-responsive delivery nanosystems reverse immunosuppression for enhanced CO gas/immunotherapy. Exploration (Beijing) 2023; 3: 20220140. https://doi.org/10.1002/EXP.20220140.

[155]

Parimi DS, Gupta Y, Marpu S, Bhatt CS, Bollu TK, Suresh AK. Nanomagnet-facilitated pharmaco-compatibility for cancer diagnostics: underlying risks and the emergence of ultrasmall nanomagnets. J Pharm Anal 2022; 12: 365-79. https://doi.org/10.1016/j.jpha.2021.11.002.

[156]

Nakamura Y, Nakano N, Ishimaru K, Hara M, Ikegami T, Tahara Y, et al. Circadian regulation of allergic reactions by the mast cell clock in mice. J Allergy Clin Immunol 2014; 133: 568-575.e12. https://doi.org/10.1016/j.jaci.2013.07.040.

[157]

Pan X, Jiang XC, Hussain MM. Impaired cholesterol metabolism and enhanced atherosclerosis in clock mutant mice. Circulation 2013; 128: 1758-69. https://doi.org/10.1161/CIRCULATIONAHA.113.002885.

[158]

Rey-Serra C, Tituaña J, Lin T, Herrero JI, Miguel V, Barbas C, et al. Reciprocal regulation between the molecular clock and kidney injury. Life Sci Alliance 2023; 6: 6. https://doi.org/10.26508/lsa.202201886.

[159]

Bellet MM, Deriu E, Liu JZ, Grimaldi B, Blaschitz C, Zeller M, et al. Circadian clock regulates the host response to salmonella. Proc Natl Acad Sci USA 2013; 110: 9897-902. https://doi.org/10.1073/pnas.1120636110.

[160]

Hashiramoto A, Yamane T, Tsumiyama K, Yoshida K, Komai K, Yamada H, et al. Mammalian clock gene Cryptochrome regulates arthritis via proinflammatory cytokine TNF-alpha. J Immunol 2010; 184: 1560-5. https://doi.org/10.4049/jimmunol.0903284.

[161]

Logan RW, Wynne O, Levitt D, Price D, Sarkar DK. Altered circadian expression of cytokines and cytolytic factors in splenic natural killer cells of Per1(−/−) mutant mice. J Interf Cytokine Res 2013; 33: 108-14. https://doi.org/10.1089/jir.2012.0092.

[162]

Luo Y, Tian W, Cai L, Wang Y, Zhang J, Teng H, et al. Expression profiling reveals a positive regulation by mPer2 on circadian rhythm of cytotoxicity receptors: Ly49C and Nkg2d. Chronobiol Int 2009; 26: 1514-44. https://doi.org/10.3109/07420520903553435.

[163]

Han Y, Meng F, Venter J, Wu N, Wan Y, Standeford H, et al. miR-34a-dependent overexpression of Per1 decreases cholangiocarcinoma growth. J Hepatol 2016; 64: 1295-304. https://doi.org/10.1016/j.jhep.2016.02.024.

[164]

He R, Zhang S, Yu J, Yu X, Wang J, Qiu Y, et al. Per1/Per2 knockout affects spleen immune function in elderly mice via inducing spleen lymphocyte ferroptosis. Int J Mol Sci 2022; 23: 12962. https://doi.org/10.3390/ijms232112962.

[165]

Arjona A, Sarkar DK. The circadian gene mPer2 regulates the daily rhythm of IFN-gamma. J Interf Cytokine Res 2006; 26: 645-9. https://doi.org/10.1089/jir.2006.26.645.

[166]

Gibbs JE, Blaikley J, Beesley S, Matthews L, Simpson KD, Boyce SH, et al. The nuclear receptor REV-ERBα mediates circadian regulation of innate immunity through selective regulation of inflammatory cytokines. Proc Natl Acad Sci USA 2012; 109: 582-7. https://doi.org/10.1073/pnas.1106750109.

[167]

Sun L, Huang K, Deng Q, Zhu Y, Cao Y, Dong K, et al. REV-ERBα negatively regulates NLRP6 transcription and reduces the severity of salmonella infection in mice. Heliyon 2024; 10: e28432. https://doi.org/10.1016/j.heliyon.2024.e28432.

[168]

Sato S, Sakurai T, Ogasawara J, Takahashi M, Izawa T, Imaizumi K, et al. A circadian clock gene, rev-erbα, modulates the inflammatory function of macrophages through the negative regulation of Ccl2 expression. J Immunol 2014; 192: 407-17. https://doi.org/10.4049/jimmunol.1301982.

[169]

Abo SMC, Layton AT. Modeling the circadian regulation of the immune system: sexually dimorphic effects of shift work. PLoS Comput Biol 2021; 17: e1008514. https://doi.org/10.1371/journal.pcbi.1008514.

[170]

Cui L, Xu F, Wang S, Li X, Lin H, Ding Y, et al. Pharmacological activation of rev-erbα suppresses LPS-induced macrophage M1 polarization and prevents pregnancy loss. BMC Immunol 2021; 22: 57. https://doi.org/10.1186/s12865-021-00438-4.

[171]

Hong H, Cheung YM, Cao X, Wu Y, Li C, Tian XY. REV-ERBα agonist SR9009 suppresses IL-1β production in macrophages through BMAL1-dependent inhibition of inflammasome. Biochem Pharmacol 2021; 192: 114701. https://doi.org/10.1016/j.bcp.2021.114701.

[172]

Ishimaru K, Nakajima S, Yu G, Nakamura Y, Nakao A. The putatively specific synthetic REV-ERB agonist SR9009 inhibits IgE-and IL-33-mediated mast cell activation independently of the circadian clock. Int J Mol Sci 2019; 20: 6320. https://doi.org/10.3390/ijms20246320.

[173]

Pariollaud M, Gibbs JE, Hopwood TW, Brown S, Begley N, Vonslow R, et al. Circadian clock component REV-ERBα controls homeostatic regulation of pulmonary inflammation. J Clin Invest 2018; 128: 2281-96. https://doi.org/10.1172/JCI93910.

[174]

Popov D, Jain L, Alhilali M, Dalbeth N, Poulsen RC. Monosodium urate crystals alter the circadian clock in macrophages leading to loss of NLRP3 inflammasome repression: implications for timing of the gout flare. FASEB J 2023; 37: e22940. https://doi.org/10.1096/fj.202202035R.

[175]

Gagnidze K, Hajdarovic KH, Moskalenko M, Karatsoreos IN, McEwen BS, Bulloch K. Nuclear receptor REV-ERBα mediates circadian sensitivity to mortality in murine vesicular stomatitis virus-induced encephalitis. Proc Natl Acad Sci USA 2016; 113: 5730-5. https://doi.org/10.1073/pnas.1520489113.

[176]

Delerive P, Monté D, Dubois G, Trottein F, Fruchart-Najib J, Mariani J, et al. The orphan nuclear receptor ROR alpha is a negative regulator of the inflammatory response. EMBO Rep 2001; 2: 42-8. https://doi.org/10.1093/embo-reports/kve007.

[177]

Stapleton CM, Jaradat M, Dixon D, Kang HS, Kim SC, Liao G, et al. Enhanced susceptibility of staggerer (RORalphasg/sg) mice to lipopolysaccharide-induced lung inflammation. Am J Physiol Lung Cell Mol Physiol 2005; 289: L144-52. https://doi.org/10.1152/ajplung.00348.2004.

PDF (1479KB)

0

Accesses

0

Citation

Detail

Sections
Recommended

/

〈 〉