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试验与肾脏疾病。

Trail and kidney disease.

作者信息

Lorz Corina, Benito Alberto, Ucero Alvaro C, Santamaría Beatriz, Ortiz Alberto

机构信息

Renal and Vascular Research Laboratory, Fundacion Jimenez Diaz-UAM, Madrid, Spain.

出版信息

Front Biosci (Landmark Ed). 2009 Jan 1;14(10):3740-9. doi: 10.2741/3485.

Abstract

TNF-related apoptosis-inducing ligand (TRAIL, TNFSF10) is a cytokine belonging to the TNF superfamily that has been recently linked to the pathogenesis of diabetic nephropathy. TRAIL may modulate cell survival and proliferation through interaction with two different receptors, TRAIL-R1 and TRAIL-R2, and the actions of TRAIL are regulated by three decoy receptors, TRAIL-R3, TRAIL-R4 and osteoprotegerin. Both TRAIL and their receptors are expressed by renal cells. In diabetic nephropathy the glomerular and tubulointerstitial expression of TRAIL is increased, and in tubular cells proinflammatory cytokines enhance TRAIL expression. Additionally, a high glucose microenvironment sensitizes tubular cells to apoptosis induced by TRAIL. Renal expression of OPG is increased in diabetic nephropathy and OPG counteracts the actions of TRAIL in cultured cells. Overall these data point to a role of TRAIL in the pathogenesis of diabetic nephropathy through interactions with other cytokines and hyperglycemia.

摘要

肿瘤坏死因子相关凋亡诱导配体(TRAIL,TNFSF10)是一种属于肿瘤坏死因子超家族的细胞因子,最近被认为与糖尿病肾病的发病机制有关。TRAIL可通过与两种不同受体TRAIL-R1和TRAIL-R2相互作用来调节细胞存活和增殖,而TRAIL的作用则受三种诱饵受体TRAIL-R3、TRAIL-R4和骨保护素的调控。TRAIL及其受体均在肾细胞中表达。在糖尿病肾病中,肾小球和肾小管间质中TRAIL的表达增加,并且在肾小管细胞中促炎细胞因子可增强TRAIL的表达。此外,高糖微环境使肾小管细胞对TRAIL诱导的凋亡敏感。糖尿病肾病中骨保护素的肾脏表达增加,且骨保护素可在培养细胞中抵消TRAIL的作用。总体而言,这些数据表明TRAIL通过与其他细胞因子和高血糖的相互作用在糖尿病肾病发病机制中发挥作用。

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