Suppr超能文献

2型糖尿病中的未折叠蛋白反应及协调的未折叠蛋白反应

UPR and coordinated UPR in type 2 diabetes.

作者信息

Kang Zhanfang, Chen Feng, Wu Wanhui, Liu Rui, Chen Tianda, Xu Fang

机构信息

Department of Basic Medical Research, Qingyuan People's Hospital, The Sixth Affiliated Hospital of Guangzhou Medical University, Qingyuan, China.

Guangzhou Municipal and Guangdong Provincial Key Laboratory of Protein Modification and Degradation, School of Basic Medical Sciences, Guangzhou Medical University, Guangzhou, China.

出版信息

Front Cell Dev Biol. 2022 Sep 16;10:974083. doi: 10.3389/fcell.2022.974083. eCollection 2022.

Abstract

The mitochondrial unfolded protein response (UPR) is a molecular mechanism that maintains mitochondrial proteostasis under stress and is closely related to various metabolic diseases, such as type 2 diabetes (T2D). Similarly, the unfolded protein response of the endoplasmic reticulum (UPR) is responsible for maintaining proteomic stability in the endoplasmic reticulum (ER). Since the mitochondria and endoplasmic reticulum are the primary centers of energy metabolism and protein synthesis in cells, respectively, a synergistic mechanism must exist between UPR and UPR to cooperatively resist stresses such as hyperglycemia in T2D. Increasing evidence suggests that the protein kinase RNA (PKR)-like endoplasmic reticulum kinase (PERK) signaling pathway is likely an important node for coordinating UPR and UPR. The PERK pathway is activated in both UPR and UPR, and its downstream molecules perform important functions. In this review, we discuss the mechanisms of UPR, UPR and their crosstalk in T2D.

摘要

线粒体未折叠蛋白反应(UPR)是一种在应激状态下维持线粒体蛋白质稳态的分子机制,与2型糖尿病(T2D)等多种代谢性疾病密切相关。同样,内质网未折叠蛋白反应(UPR)负责维持内质网(ER)中的蛋白质组稳定性。由于线粒体和内质网分别是细胞中能量代谢和蛋白质合成的主要中心,因此UPR和UPR之间必然存在一种协同机制,以协同抵抗T2D中的高血糖等应激。越来越多的证据表明,蛋白激酶RNA(PKR)样内质网激酶(PERK)信号通路可能是协调UPR和UPR的重要节点。PERK通路在UPR和UPR中均被激活,其下游分子发挥重要作用。在本综述中,我们讨论了UPR、UPR的机制及其在T2D中的相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2597/9523447/7448ca7d5f9b/fcell-10-974083-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验