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YAP:代谢与心脏重构之间的联系。

YAP: The nexus between metabolism and cardiac remodeling.

机构信息

Department of Pharmacology and Systems Physiology, University of Cincinnati, Cincinnati, Ohio, USA.

Program in Cardiovascular and Metabolic Diseases, Duke-NUS, Singapore.

出版信息

J Clin Invest. 2022 Mar 15;132(6). doi: 10.1172/JCI157664.

Abstract

Cardiomyocyte hypertrophy is an integral part of cardiac remodeling that occurs under physiological or pathological stresses. It can lead to heart failure in a pathological form or oppose functional deterioration in a compensatory one. The mechanisms underlying an adaptive outcome of hypertrophy are ill defined. In this issue of the JCI, Kashihara et al. explored the role of the Yes-associated protein 1 (YAP) transcription factor in the heart, using cell culturing and mouse models. YAP activity was found to be associated with changes in genes of the glycolytic and auxiliary pathways under stress. Notably, YAP upregulated glucose transporter 1 (GLUT1), and inhibition of GLUT1 blocked YAP-induced hypertrophy but worsened heart function. These findings suggest that YAP is a regulator of metabolic reprogramming in the heart during compensatory hypertrophy. This insight may help in the development of future therapies for heart failure.

摘要

心肌细胞肥大是在生理或病理应激下发生的心脏重构的一个组成部分。它可以导致病理性心力衰竭,或者在代偿性心力衰竭中对抗功能恶化。肥大的适应性结果的机制还不清楚。在本期 JCI 中,Kashihara 等人使用细胞培养和小鼠模型探索了 Yes 相关蛋白 1(YAP)转录因子在心脏中的作用。研究发现,YAP 的活性与应激下糖酵解和辅助途径基因的变化有关。值得注意的是,YAP 上调葡萄糖转运蛋白 1(GLUT1),抑制 GLUT1 阻断了 YAP 诱导的肥大,但恶化了心脏功能。这些发现表明,YAP 是代偿性肥大过程中心脏代谢重编程的调节剂。这一见解可能有助于未来心力衰竭治疗的发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/754e/8920320/e75e66051205/jci-132-157664-g071.jpg

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