Tea Polyphenols Reduce Inflammation of Orbital Fibroblasts in Graves’ Ophthalmopathy via the NF-κB/NLRP3 Pathway

Wei Liu , Chao Ma , Hao-yu Li , Shan-si Yuan , Kai-jun Li

Current Medical Science ›› 2023, Vol. 43 ›› Issue (1) : 123 -129.

PDF
Current Medical Science ›› 2023, Vol. 43 ›› Issue (1) : 123 -129. DOI: 10.1007/s11596-023-2708-7
Article

Tea Polyphenols Reduce Inflammation of Orbital Fibroblasts in Graves’ Ophthalmopathy via the NF-κB/NLRP3 Pathway

Author information +
History +
PDF

Abstract

Objective

This study aimed to explore the effects of tea polyphenols (TP) on inflammation of orbital fibroblasts in Graves’ ophthalmopathy (GO) and to provide new ideas for GO treatment.

Methods

Primary orbital fibroblasts were extracted from orbital adipose/connective tissues of patients with and without GO. Real-time quantitative PCR (RT-qPCR) was used to detect the expression of interleukin (IL)-6, IL-1β, and monocyte chemotactic protein (MCP)-1 in non-GO and GO orbital fibroblasts. The CCK-8 assay was used to determine the appropriate concentration of TP for subsequent experiments. RT-qPCR and enzyme-linked immunosorbent assay (ELISA) were performed to investigate the effects of TP on lipopolysaccharide (LPS)-induced production of inflammatory cytokines. Nuclear factor-κB (NF-κB) expression was measured using Western blotting analysis. NOD-like receptor 3 (NLRP3) expression was detected using both Western blotting analysis and immunofluorescence staining.

Results

The mRNA levels of IL-6, IL-1β, and MCP-1 in GO orbital fibroblasts were significantly higher than those in non-GO cells. TP treatment significantly inhibited LPS-induced production of inflammatory factors, including IL-6, IL-1β, and MCP-1. TP also inhibited the expression levels of NF-κB and NLRP3. Inflammation in the GO orbital fibroblasts was higher than that in non-GO cells. TP inhibited the production of inflammatory cytokines in GO orbital fibroblasts in vitro through the NF-κB/NLRP3 pathway.

Conclusion

These findings suggest that TP may have a potential role in GO treatment.

Keywords

tea polyphenols / Graves’ ophthalmopathy / inflammation

Cite this article

Download citation ▾
Wei Liu, Chao Ma, Hao-yu Li, Shan-si Yuan, Kai-jun Li. Tea Polyphenols Reduce Inflammation of Orbital Fibroblasts in Graves’ Ophthalmopathy via the NF-κB/NLRP3 Pathway. Current Medical Science, 2023, 43(1): 123-129 DOI:10.1007/s11596-023-2708-7

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

JangSY, ParkSJ, ChaeMK, et al.. Role of microRNA-146a in regulation of fibrosis in orbital fibroblasts from patients with Graves’ orbitopathy. Br J Ophthalmol, 2018, 102(3): 407-414

[2]

SmithTJ. Pathogenesis of Graves’ orbitopathy: A 2010 update. J Endocrinol Invest, 2010, 33(6): 414-421

[3]

McLachlanSM, PrummelMF, RapoportB. Cell-mediated or humoral immunity in Graves’ ophthalmopathy? Profiles of T-cell cytokines amplified by polymerase chain reaction from orbital tissue. J Clin Endocrinol Metab, 1994, 78(5): 1070-1074

[4]

LeeJS, KimJ, LeeEJ, et al.. Therapeutic Effect of Curcumin, a Plant Polyphenol Extracted From Curcuma longae, in Fibroblasts From Patients With Graves’ Orbitopathy. Invest Ophthalmol Vis Sci, 2019, 60(13): 4129

[5]

YoonJS, ChaeMK, LeeSY, et al.. Anti-inflammatory effect of quercetin in a whole orbital tissue culture of Graves’ orbitopathy. Br J Ophthalmol, 2012, 96(8): 1117-1121

[6]

FangS, HuangY, LiuX, et al.. Interaction Between CCR6 + Th17 Cells and CD34 + Fibrocytes Promotes Inflammation: Implications in Graves’ Orbitopathy in Chinese Population. Invest Ophthalmol Vis Sci, 2018, 59(6): 2604

[7]

NiyazogluM, BaykaraO, KocA, et al.. Association of PARP-1, NF-κB, NF-κBIA and IL-6, IL-1β and TNF-α with Graves Disease and Graves Ophthalmopathy. Gene, 2014, 547(2): 226-232

[8]

CawoodTJ, MoriartyP, O’FarrellyC, et al.. The effects of tumour necrosis factor-α and interleukin1 on an in vitro model of thyroid-associated ophthalmopathy; contrasting effects on adipogenesis. Eur J Endocrinol, 2006, 155(3): 395-403

[9]

HiromatsuY, YangD, BednarczukT, et al.. Cytokine Profiles in Eye Muscle Tissue and Orbital Fat Tissue from Patients with Thyroid-Associated Ophthalmopathy. J Clin Endocrinol Metabol, 2000, 85(3): 1194-1199

[10]

PritchardJ, HorstN, CruikshankW, et al.. Igs from patients with Graves’ disease induce the expression of T cell chemoattractants in their fibroblasts. J Immunol, 2002, 168(2): 942-950

[11]

DikWA, VirakulS, van SteenselL. Current perspectives on the role of orbital fibroblasts in the pathogenesis of Graves’ ophthalmopathy. Exper Eye Res, 2016, 142: 83-91

[12]

LiH, ZhangY, MinJ, et al.. Astragaloside IV attenuates orbital inflammation in Graves’ orbitopathy through suppression of autophagy. Inflamm Res, 2018, 67(2): 117-127

[13]

OzHS, McClainCJ, NagasawaHT, et al.. Diverse antioxidants protect against acetaminophen hepatotoxicity. J Biochem Mol Toxicol, 2005, 18(6): 361-368

[14]

OzHS, ChenTS, McClainCJ, et al.. Antioxidants as novel therapy in a murine model of colitis. J Nutrit Biochem, 2005, 16(5): 297-304

[15]

CabreraC, ArtachoR, GiménezR. Beneficial Effects of Green Tea—A Review. J Am Coll Nutrit, 2006, 25(2): 79-99

[16]

MarinovicMP, MorandiAC, OttonR. Green tea catechins alone or in combination alter functional parameters of human neutrophils via suppressing the activation of TLR-4/NFκB p65 signal pathway. Toxicol In Vitro, 2015, 29(7): 1766-1778

[17]

KaroriSM, NgureRM, WachiraFN, et al.. Different types of tea products attenuate inflammation induced in Trypanosoma brucei infected mice. Parasitol Int, 2008, 57(3): 325-333

[18]

LiH, MaC, LiuW, et al.. Gypenosides Protect Orbital Fibroblasts in Graves Ophthalmopathy via Anti-Inflammation and Anti-Fibrosis Effects. Invest Ophthalmol Vis Sci, 2020, 61(5): 64

[19]

LiyanageNM, LeeH-G, NagahawattaDP, et al.. Characterization and therapeutic effect of Sargassum coreanum fucoidan that inhibits lipopolysaccharide-induced inflammation in RAW 264.7 macrophages by blocking NF-kB signaling. Int J Biol Macromol, 2022, 223: 500-510 PtA

[20]

YiW-S, XuX-L. Effects of LPS-induced inflammation on differentiation of orbital pre-adipocytes in thyroid-associated ophthalmopathy. Zhonghua Yan Ke Za Zhi (China), 2011, 47(2): 156-161

[21]

LuoLH, LiDM, WangYL, et al.. Tim3/galectin-9 alleviates the inflammation of TAO patients via suppressing Akt/NF-kB signaling pathway. Biochem Biophys Res Commun, 2017, 491(4): 966-972

[22]

ChengYC, SheenJM, HuWL, et al.. Polyphenols and Oxidative Stress in Atherosclerosis-Related Ischemic Heart Disease and Stroke. Oxid Med Cell Longev, 2017, 2017: 1-16

[23]

ZhangS, LiuX, MeiL, et al.. Epigallocatechin-3-gallate (EGCG) inhibits imiquimod-induced psoriasis-like inflammation of BALB/c mice. BMC Complement Altern Med, 2016, 16(1): 334

[24]

BachmaierK, ToyaS, GaoX, et al.. E3 ubiquitin ligase Cblb regulates the acute inflammatory response underlying lung injury. Nat Med, 2007, 13(8): 920-926

[25]

CaoB, WangT, QuQ, et al.. Long Noncoding RNA SNHG1 Promotes Neuroinflammation in Parkinson’s Disease via Regulating miR-7/NLRP3 Pathway. Neuroscience, 2018, 388: 118-127

[26]

WangY, CuiY, CaoF, et al.. Ganglioside GD1a suppresses LPS-induced pro-inflammatory cytokines in RAW264.7 macrophages by reducing MAPKs and NF-κB signaling pathways through TLR4. Int Immunopharmacol, 2015, 28(1): 136-145

[27]

XiangP, ChenT, MouY, et al.. NZ suppresses TLR4/NF-κB signalings and NLRP3 inflammasome activation in LPS-induced RAW264.7 macrophages. Inflamm Res, 2015, 64(10): 799-808

[28]

LatzE, XiaoTS, StutzA. Activation and regulation of the inflammasomes. Nat Rev Immunol, 2013, 13(6): 397-411

[29]

WuX, DongL, LinX, et al.. Relevance of the NLRP3 Inflammasome in the Pathogenesis of Chronic Liver Disease. Front Immunol, 2017, 8: 1728

[30]

WangD, ZhangM, WangT, et al.. Green tea polyphenols prevent lipopolysaccharide-induced inflammatory liver injury in mice by inhibiting NLRP3 inflammasome activation. Food Funct, 2019, 10(7): 3898-3908

AI Summary AI Mindmap
PDF

82

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/