[1]王文颜,张学东.NLRP3炎症小体在糖尿病视网膜病变中的作用[J].眼科新进展,2018,38(6):587-591.[doi:10.13389/j.cnki.rao.2018.0139]
 WANG Wen-Yan,ZHANG Xue-Dong.The role and research progress of NLRP3 inflammasome in diabetic retinopathy[J].Recent Advances in Ophthalmology,2018,38(6):587-591.[doi:10.13389/j.cnki.rao.2018.0139]
点击复制

NLRP3炎症小体在糖尿病视网膜病变中的作用/HTML
分享到:

《眼科新进展》[ISSN:1003-5141/CN:41-1105/R]

卷:
38卷
期数:
2018年6期
页码:
587-591
栏目:
文献综述
出版日期:
2018-06-05

文章信息/Info

Title:
The role and research progress of NLRP3 inflammasome in diabetic retinopathy
作者:
王文颜张学东
400010 重庆市,重庆医科大学附属第一医院眼科 重庆市眼科研究所 眼科学重庆市市级重点实验室
Author(s):
WANG Wen-YanZHANG Xue-Dong
Ophthalmology,the First Affiliated Hospital of Chongqing Medical University,Chongqing Key Laboratory of Ophthalmology,Chongqing Eye Institute,Chongqing 400010,China
关键词:
糖尿病视网膜病变NLRP3炎症小体治疗靶点
Keywords:
diabetic retinopathy NLRP3 inflammasometargets for therapy
分类号:
R774.1
DOI:
10.13389/j.cnki.rao.2018.0139
文献标志码:
A
摘要:
糖尿病视网膜病变(diabetic retinopathy,DR)是糖尿病导致的严重微血管并发症之一。目前,对于DR确切的发病机制仍无定论。近期研究表明,炎症与自身免疫反应在DR的发生发展中起着重要作用。核苷酸结合寡聚化结构域样受体蛋白3(nucleotide-binding domain and leucine-rich repeat receptor containing a pyrin domain 3,NLRP3)炎症小体能触发各种炎症反应,并在多种慢性炎症性疾病中发挥重要作用。现已有不少研究证实NLRP3炎症小体通过参与多条通路在DR中发挥促炎作用,提示通过抑制NLPR3炎症小体或者其参与的通路或许可成为DR治疗新靶点。本文就NLRP3炎症小体在DR发病中的作用作一综述。
Abstract:
Diabetic retinopathy (DR) is one of the severe microvascular complications caused by diabetes,and the precise pathogenesis of DR is still unsettled now.Recent studies have shown that inflammation and autoimmune responses play important roles in the development of DR.Nucleotide-binding domain and leucine-rich repeat receptor containing a pyrin domain 3 (NLRP3) inflammasome can trigger a variety of inflammatory responses and involves in various chronic inflammatory diseases.At present,a large number of studies have confirmed that NLRP3 inflammasome promotes inflammatory responses in DR through multiple pathways,which have suggested that inhibition of NLPR3 inflammasome or its involved pathways may have therapeutic effects on DR,and the role of NLRP3 inflammasome in DR will be reviewed in this article.

参考文献/References:

[1] NOLAN C J,DAMM P,PRENTKI M.Type 2 diabetes across generations:from pathophysiology to prevention and management[J].Lancet,2011,378(9786):169-181.
[2] SAADDINE J B,HONEYCUTT A A,NARAYAN K M,ZHANG X,KLEIN R,BOYLE J P.Projection of diabetic retinopathy and other major eye diseases among people with diabetes mellitus:United States,2005-2050[J].Arch Ophthalmol,2008,126(12):1740-1747.
[3] GIACCO F,BROWNLE E M.Oxidative stress and diabetic complications[J].Circ Res,2010,107(9):1058-1070.
[4] CHEN M,CURTIS T M,STITT A W.Advanced glycation end products and diabetic retinopathy[J].Curr Med Chem,2013,20(26):3234-3240.
[5] GALVEZ M I.Protein kinase C inhibitors in the treatment of diabetic retinopathy.Review[J].Curr Pharm Biotechnol,2011,12(3):386-391.
[6] TOMIC M,LJUBIC S,KASTELAN S.The role of inflammation and endothelial dysfunction in the pathogenesis of diabetic retinopathy[J].Coll Antropol,2013,37(Suppl 1):51-57.
[7] GUO H,CALLAWAY J B,TING J P Y.Inflammasomes:mechanism of action,role in disease and therapeutics[J].Nat Med,2015,21(7):677-687.
[8] KAUPPINEN A,NISKANEN H,SUURONEN T,KINNUNEN K,SALMINEN A,KAARNIRANTA K.Oxidative stress activates NLRP3 inflammasomes in ARPE-19 cells--implications for age-related macular degeneration(AMD)[J].Immunol Lett,2012,147(1-2):29-33.
[9] YIN Y,CHEN F,WANG W,WANG H,ZHANG X.Resolvin D1 inhibits inflammatory response in STZ-induced diabetic retinopathy rats:Possible involvement of NLRP3 inflammasome and NF-kappaB signaling pathway[J].Mol Vis,2017,23:242-250.
[10] CHEN W,ZHAO M,ZHAO S,LU Q,NI L,ZOU C,et al.Activation of the TXNIP/NLRP3 inflammasome pathway contributes to inflammation in diabetic retinopathy:a novel inhibitory effect of minocycline[J].Inflamm Res,2017,66(2):157-166.
[11] SHI H,ZHANG Z,WANG X,LI R,HOU W,BI W,et al.Inhibition of autophagy induces IL-1beta release from ARPE-19 cells via ROS mediated NLRP3 inflammasome activation under high glucose stress[J].Biochem Biophys Res Commun,2015,463(4):1071-1076.
[12] CHEUNG N,MITCHELL P,WONG T Y.Diabetic retinopathy[J].Lancet,2010,376(9735):124-136.
[13] LOUKOVAARA S,PIIPPO N,KINNUNEN K,HYTTI M,KAARNIRANTA K,KAUPPINEN A.NLRP3 inflammasome activation is associated with proliferative diabetic retinopathy[J].Acta Ophthalmol,2017,95(8):803-808.
[14] ZHANG Y,LV X,HU Z,YE X,ZHENG X,DING Y,et al.Protection of Mcc950 against high-glucose-induced human retinal endothelial cell dysfunction[J].Cell Death Dis,2017,8(7):e2941.
[15] CHAURASIA S S,LIM R R,PARIKH B H,WEY Y S,TUN B B,WONG T Y,et al.The NLRP3 inflammasome may contribute to pathologic neovascularization in the advanced stages of diabetic retinopathy[J].Sci Rep,2018,8(1):2847.
[16] BARBER A J,GARDNER T W,ABCOUWER S F.The significance of vascular and neural apoptosis to the pathology of diabetic retinopathy[J].Invest Ophthalmol Vis Sci,2011,52(2):1156-1163.
[17] DEVI T S,HOSOYA K,TERASAKI T,SINGH L P.Critical role of TXNIP in oxidative stress,DNA damage and retinal pericyte apoptosis under high glucose:implications for diabetic retinopathy[J].Exp Cell Res,2013,319(7):1001-1012.
[18] PERRONE L,DEVI T S,HOSOYA K I,TERASAKI T,SINGH L P.Inhibition of TXNIP expression in vivo blocks early pathologies of diabetic retinopathy[J].Cell Death Dis,2010,1:e65.
[19] LERNER A G,UPTON J P,PRAVEEN P V,GHOSH R,NAKAGAWA Y,IGBARIA A,et al.IRE1alpha induces thioredoxin-interacting protein to activate the NLRP3 inflammasome and promote programmed cell death under irremediable ER stress[J].Cell Metab,2012,16(2):250-264.
[20] ZHOU R,TARDIVEL A,THORENS B,CHOI I,TSCHOPP J.Thioredoxin-interacting protein links oxidative stress to inflammasome activation[J].Nat Immunol,2010,11(2):136-140.
[21] KERN T S.Contributions of inflammatory processes to the development of the early stages of diabetic retinopathy[J].Exp Diabetes Res,2007,2007:95103.
[22] KOWLUR R A,KOPPOLU P,CHAKRABARTI S,CHEN S.Diabetes-induced activation of nuclear transcriptional factor in the retina,and its inhibition by antioxidants[J].Free Radic Res,2003,37(11):1169-1180.
[23] KARBASFOROOSHAN H,KARIMI G.The role of SIRT1 in diabetic retinopathy[J].Biomed Pharmacother,2018,97:190-194.
[24] SHAO A,WU H,HONG Y,TU S,SUN X,WU Q.Hydrogen-rich saline attenuated subarachnoid hemorrhage-induced early brain injury in rats by suppressing inflammatory response:possible involvement of NF-kappaB pathway and NLRP3 inflammasome[J].Mol Neurobiol,2016,53(5):3462-3476.
[25] SAMRA Y A,SAID H S,ELSHERBINY N M,LIOU G I,El-SHISHTAWY M M,EISSA L A.Cepharanthine and Piperine ameliorate diabetic nephropathy in rats:role of NF-kappaB and NLRP3 inflammasome[J].Life Sci,2016,157:187-199.
[26] YANG S M,KA S M,WU H L,YEH Y C,KUO C H,HUA K F,et al.Thrombomodulin domain 1 ameliorates diabetic nephropathy in mice via anti-NF-kappaB/NLRP3 inflammasome-mediated inflammation,enhancement of NRF2 antioxidant activity and inhibition of apoptosis[J].Diabetologia,2014,57(2):424-434.
[27] CHI W,CHEN H,LI F,ZHU Y,YIN W,ZHUO Y.HMGB1 promotes the activation of NLRP3 and caspase-8 inflammasomes via NF-kappaB pathway in acute glaucoma[J].J Neuroinflammation,2015,12:137.
[28] LIU R T,WANG A,TO E,GAO J,CAO S,CUI J Z,et al.Vinpocetine inhibits amyloid-beta induced activation of NF-kappaB,NLRP3 inflammasome and cytokine production in retinal pigment epithelial cells[J].Exp Eye Res,2014,127:49-58.
[29] RUIZ S,PERGOLA P E,ZAGER R A,VAZIRI N D.Targeting the transcription factor Nrf2 to ameliorate oxidative stress and inflammation in chronic kidney disease[J].Kidney Int,2013,83(6):1029-1041.
[30] CHEN W J,WU C,XU Z,KUSE Y,HARA H,DUH E J.Nrf2 protects photoreceptor cells from photo-oxidative stress induced by blue light[J].Exp Eye Res,2017,154:151-158.
[31] XU Z,WEI Y,GONG J,CHO H,PARK J K,SUNG E R,et al.NRF2 plays a protective role in diabetic retinopathy in mice[J].Diabetologia,2014,57(1):204-213.
[32] CAO Y,LI X,WANG C J,LI P,YANG B,WANG C B,et al.Role of NF-E2-related factor 2 in neuroprotective effect of l-carnitine against high glucose-induced oxidative stress in the retinal ganglion cells[J].Biomed Pharmacother,2015,69:345-348.
[33] LIU X,ZHANG X,DING Y,ZHOU W,TAO L,LU P,et al.Nuclear factor E2-related factor-2 negatively regulates NLRP3 inflammasome activity by inhibiting reactive oxygen species-induced NLRP3 priming[J].Antioxid Redox Signal,2017,26(1):28-43.
[34] LIU Q,ZHANG F,ZHANG X,CHENG R,MA J X,YI J,et al.Fenofibrate ameliorates diabetic retinopathy by modulating Nrf2 signaling and NLRP3 inflammasome activation[J].Mol Cell Biochem,2017.
[35] GUO C X,TRAN H,GREEN C R,DANESH-MEYER H V,ACOSTA M L.Gap junction proteins in the light-damaged albino rat[J].Mol Vis,2014,20:670-682.
[36] MUGISHO O O,GREEN C R,KHO D T,ZHANG J,GRAHAM E S,ACOSTA M L,et al.The inflammasome pathway is amplified and perpetuated in an autocrine manner through connexin43 hemichannel mediated ATP release[J].Biochim Biophys Acta,2018,1862(3):385-393.
[37] CHEN Y S,GREEN C R,TEAGUE R,ZHANG J,GRAHAM E S,ACOSTA M L,et al.Intravitreal injection of lipoamino acid-modified connexin43 mimetic peptide enhances neuroprotection after retinal ischemia[J].Drug Deliv Transl Res,2015,5(5):480-488.
[38] JO E K,KIM J K,SHIN D M,SASAKAWA C.Molecular mechanisms regulating NLRP3 inflammasome activation[J].Cell Mol Immunol,2016,13(2):148-159.
[39] KIM Y,DAVIDSON J O,GUNN K C,PHILLIPS A R,GREEN C R,GUNN A J.Role of hemichannels in CNS inflammation and the inflammasome pathway[J].Adv Protein Chem Struct Biol,2016,104:1-37.
[40] ZHOU L,WANG Z,XU X,WAN Y,QU K,FAN H,et al.Nek7 is overexpressed in hepatocellular carcinoma and promotes hepatocellular carcinoma cell proliferation in vitro and in vivo[J].Oncotarget,2016,7(14):18620-18630.
[41] SHI H,WANG Y,LI X,ZHAN X,TANG M,FINA M,et al.NLRP3 activation and mitosis are mutually exclusive events coordinated by NEK7,a new inflammasome component[J].Nat Immunol,2016,17(3):250-258.
[42] HE Y,ZENG M Y,YANG D,MOTRO B,NUNEZ G.NEK7 is an essential mediator of NLRP3 activation downstream of potassium efflux[J].Nature,2016,530(7590):354-357.
[43] WANG C,PAN Y,ZHANG Q Y,WANG F M,KONG L D.Quercetin and allopurinol ameliorate kidney injury in STZ-treated rats with regulation of renal NLRP3 inflammasome activation and lipid accumulation[J].PLoS One,2012,7(6):e38285.
[44] RAN Y,CHEN J Z,The research progress of NLRP3 inflammasome and type 2 diabetes [J].Chin J Cell Mol Immunol,2013,(12):1327-1329.

相似文献/References:

[1]杜玮 刘子扬 周艳艳 雒雷鸣.糖尿病视网膜病变与血清胆红素水平的关系[J].眼科新进展,2012,32(5):000.
[2]范松涛 卢建民.阿司匹林与糖尿病患者玻璃体出血以及玻璃体切割术疗效的相关性研究[J].眼科新进展,2012,32(11):000.
[3]李艳 李筱荣 袁佳琴 潘斌.糖尿病大鼠视网膜中VEGF、PEDF的表达与血-视网膜屏障损伤[J].眼科新进展,2013,33(1):000.
[4]李朝晖 崔治华 胡晓英 孟丽珠 张敬维.糖尿病视网膜病变激光面积与疗效的分析[J].眼科新进展,2013,33(2):000.
[5]冯冬梅 朱鸿 施彩虹.CXC趋化因子及其受体在糖尿病视网膜病变中的作用[J].眼科新进展,2013,33(6):000.
[6]牛淑玲.糖尿病视网膜病变患者HbAlc、FPG与血小板参数的变化及危险因素分析[J].眼科新进展,2013,33(7):000.
[7]毕春潮 王睿 王建洲 雷春灵 董晓娟 王小莉 薛晓辉.Ad-PEDF对糖尿病视网膜病变大鼠视网膜新生血管的抑制作用[J].眼科新进展,2013,33(8):000.
[8]杨萍 孙书明 李晓鹏.辛伐他汀对糖尿病视网膜病变和炎症因子的影响[J].眼科新进展,2013,33(8):000.
[9]罗文婷 孙大卫.血管黏附蛋白-1在眼科疾病中的研究进展[J].眼科新进展,2013,33(8):000.
[10]李小璐 马雅玲.糖尿病视网膜病变大鼠视网膜VEGF和PEDF的动态表达[J].眼科新进展,2013,33(9):000.
[11]姚国敏,李蓉,闫红林,等.高糖诱导的视网膜新生血管形成中NLRP3炎症小体与自噬的关系研究[J].眼科新进展,2020,40(8):706.[doi:10.13389/j.cnki.rao.2020.0161]
 YAO Guomin,LI Rong,YAN Honglin,et al.Relationship between NLRP3 inflammasome and autophagy in high-glucose induced retinal angiogenesis[J].Recent Advances in Ophthalmology,2020,40(6):706.[doi:10.13389/j.cnki.rao.2020.0161]
[12]黎晓冬,谢学军,宿晓娟,等.GSDMD介导的细胞焦亡在糖尿病视网膜病变中的研究进展[J].眼科新进展,2021,41(12):1187.[doi:10.13389/j.cnki.rao.2021.0248]
 LI Xiaodong,XIE Xuejun,SU Xiaojuan,et al.Advances in the treatment of diabetic retinopathy by gasdermin D mediated pyroptosis[J].Recent Advances in Ophthalmology,2021,41(6):1187.[doi:10.13389/j.cnki.rao.2021.0248]

备注/Memo

备注/Memo:
国家自然科学基金资助(编号:81371843)
更新日期/Last Update: 2018-07-10