内皮细胞中的自噬可以控制血流介导的血管反应性和重塑,并调节VEGFR2亚细胞定位和信号传导

Pierre-Louis Tharaux, Olivia Lenoir
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引用次数: 0

摘要

旨在增加自噬通量和内皮细胞自噬缺陷的基因工程小鼠的药理学方法表明,自噬对代谢应激和血管老化具有血管保护作用。然而,内皮细胞中自噬控制的特定细胞过程的身份仍不清楚。在这篇文章中,我们讨论了内皮细胞中自噬的多种功能的最新发现。特别是,我们强调自噬控制血流介导的血管反应性和重塑。我们还关注了自噬机制在调节细胞内蛋白质分布中的作用,以及自噬如何调节细胞对微环境变化的反应的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Autophagy in the endothelium commands flow-mediated vascular reactivity and remodelling, and regulates VEGFR2 subcellular localization and signalling
Pharmacological approaches aimed at increasing autophagic flux and genetically engineered mice with autophagy deficiency in the endothelium have demonstrated that autophagy exerts vessel protection against metabolic stresses and vascular aging. However, the identity of the specific cellular processes that autophagy controls in endothelial cells remained unclear. In this punctum, we discuss our recent findings on the multiple functions of autophagy in the endothelium. Particularly, we highlighted that autophagy controls flow-mediated vascular reactivity and remodeling. We have also focused on the role of autophagy machinery in regulating protein distribution within the cell and on the results demonstrating how autophagy modulates the cellular response to the microenvironment changes.
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