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细胞焦亡新机制及其在糖尿病肾病中的作用。

New Insights into the Mechanisms of Pyroptosis and Implications for Diabetic Kidney Disease.

机构信息

ZJU-UoE Institute, International Campus, Zhejiang University, Haining 314400, China.

Kidney Disease Center, The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou 310003, China.

出版信息

Int J Mol Sci. 2020 Sep 25;21(19):7057. doi: 10.3390/ijms21197057.

Abstract

Pyroptosis is one special type of lytic programmed cell death, featured in cell swelling, rupture, secretion of cell contents and remarkable proinflammation effect. In the process of pyroptosis, danger signalling and cellular events are detected by inflammasome, activating caspases and cleaving Gasdermin D (GSDMD), along with the secretion of IL-18 and IL-1β. Pyroptosis can be divided into canonical pathway and non-canonical pathway, and NLRP3 inflammasome is the most important initiator. Diabetic kidney disease (DKD) is one of the most serious microvascular complications in diabetes. Current evidence reported the stimulatory role of hyperglycaemia-induced cellular stress in renal cell pyroptosis, and different signalling pathways have been shown to regulate pyroptosis initiation. Additionally, the inflammation and cellular injury caused by pyroptosis are tightly implicated in DKD progression, aggravating renal fibrosis, glomerular sclerosis and tubular injury. Some registered hypoglycaemia agents exert suppressive activity in pyroptosis regulation pathway. Latest studies also reported some potential approaches to target the pyroptosis pathway, which effectively inhibits renal cell pyroptosis and alleviates DKD in in vivo or in vitro models. Therefore, comprehensively compiling the information associated with pyroptosis regulation in DKD is the main aim of this review, and we try to provide new insights for researchers to dig out more potential therapies of DKD.

摘要

细胞焦亡是一种特殊的细胞程序性死亡方式,其特征为细胞肿胀、破裂,细胞内容物的释放,并伴有明显的促炎作用。在细胞焦亡过程中,危险信号和细胞事件被炎性小体检测到,激活半胱天冬酶并切割 Gasdermin D(GSDMD),同时释放白细胞介素-18(IL-18)和白细胞介素-1β(IL-1β)。细胞焦亡可分为经典途径和非经典途径,NLRP3 炎性小体是最重要的起始因子。糖尿病肾病(DKD)是糖尿病最严重的微血管并发症之一。目前的证据表明,高血糖诱导的细胞应激在肾脏细胞焦亡中具有刺激作用,不同的信号通路已被证明可调节细胞焦亡的发生。此外,细胞焦亡引起的炎症和细胞损伤与 DKD 的进展密切相关,加重了肾纤维化、肾小球硬化和肾小管损伤。一些已注册的降血糖药物在细胞焦亡调节途径中具有抑制作用。最新的研究还报道了一些针对细胞焦亡途径的潜在方法,这些方法在体内或体外模型中有效抑制了肾脏细胞焦亡,减轻了 DKD。因此,全面编译与 DKD 中细胞焦亡调节相关的信息是本综述的主要目的,我们试图为研究人员提供新的见解,以挖掘出更多 DKD 的潜在治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0bc/7583981/91a404488ef9/ijms-21-07057-g001.jpg

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