Litcius/Paper detail

YAP accelerates vascular senescence via blocking autophagic flux and activating mTOR

Xianmei Pan, Bo Wu, Xianglin Fan, Guanghui Xu, Caiwen Ou, Minsheng Chen

2020Journal of Cellular and Molecular Medicine51 citationsDOIOpen Access PDF

Abstract

Yes-associated protein (YAP), a major effector of the Hippo signalling pathway, is widely implicated in vascular pathophysiology processes. Here, we identify a new role of YAP in the regulation of vascular senescence. The inhibition or deficiency and overexpression of YAP were performed in human umbilical vein endothelial cells (HUVECs) and isolated vascular tissues. Cellular and vascular senescence was assessed by analysis of the senescence-associated β-galactosidase (SA-β-gal) and expression of senescence markers P16, P21, P53, TERT and TRF1. We found that YAP was highly expressed in old vascular tissues, inhibition and knockdown of YAP decreased senescence, while overexpression of YAP increased the senescence in both HUVECs and vascular tissues. In addition, autophagic flux blockage and mTOR pathway activation were observed during YAP-induced HUVECs and vascular senescence, which could be relieved by the inhibition and knockdown of YAP. Moreover, YAP-promoted cellular and vascular senescence could be relieved by mTOR inhibition. Collectively, our findings indicate that YAP may serve as a potential therapeutic target for ageing-associated cardiovascular disease.

Topics & Concepts

SenescenceAutophagyCell biologyPI3K/AKT/mTOR pathwayGene knockdownBiologyUmbilical veinEffectorVascular smooth muscleMechanistic target of rapamycinCancer researchSignal transductionCell cultureEndocrinologyApoptosisBiochemistryIn vitroGeneticsSmooth muscleHippo pathway signaling and YAP/TAZLipid metabolism and biosynthesisAutophagy in Disease and Therapy