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观点:线粒体 STAT3 在心脏保护中的作用。

Perspective: mitochondrial STAT3 in cardioprotection.

机构信息

Institute for Pathophysiology, West German Heart and Vascular Center, University of Essen Medical School, Hufelandstr. 55, 45122, Essen, Germany.

出版信息

Basic Res Cardiol. 2023 Aug 24;118(1):32. doi: 10.1007/s00395-023-01003-3.

Abstract

Activation of signal transducer and activator of transcription 3 (STAT3) has been identified as a key cardioprotective signal not only in animal studies but also in humans-in animals, STAT3 is causally involved in cardioprotection. In response to late ischemic conditioning, canonical function of STAT3 activation upregulates the expression of cardioprotective and anti-apoptotic proteins. In its non-canonical function, STAT3 is activated during ischemic conditioning and is part of the cardioprotective cytosolic survival activating factor enhancement pathway. Activated STAT3 is imported and localized to the mitochondria. Mitochondrial STAT3 stimulates the activity of mitochondrial electron transport chain complex I, reduces mitochondrial reactive oxygen species production and mitochondrial permeability transition pore opening. Finally, two novel aspects of STAT activation in cardioprotection are discussed: a genetic variance of the STAT encoding region as a potential primordial confounding variable for cardioprotection, and the cardioprotective potential of sodium-glucose cotransporter 2 inhibitors through STAT3 activation.

摘要

信号转导子和转录激活子 3(STAT3)的激活已被确定为不仅在动物研究中,而且在人类中也是一种关键的心脏保护信号——在动物中,STAT3 因果关系地参与心脏保护。针对晚期缺血性预处理,STAT3 激活的经典功能上调心脏保护和抗细胞凋亡蛋白的表达。在其非经典功能中,STAT3 在缺血性预处理期间被激活,并且是心脏保护细胞质存活激活因子增强途径的一部分。激活的 STAT3 被导入并定位于线粒体。线粒体 STAT3 刺激线粒体电子传递链复合物 I 的活性,减少线粒体活性氧物质的产生和线粒体通透性转换孔的开放。最后,讨论了 STAT 激活在心脏保护中的两个新方面:STAT 编码区的遗传变异作为心脏保护的潜在原始混杂变量,以及钠-葡萄糖共转运蛋白 2 抑制剂通过 STAT3 激活的心脏保护潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd8d/10449977/c595a78143c5/395_2023_1003_Fig1_HTML.jpg

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