Nucleoporin93 limits Yap activity to prevent endothelial cell senescence

Tung D. Nguyen, Mihir K. Rao, Shaiva P. Dhyani, Justin M. Banks, Michael A. Winek, Julia Michalkiewicz,Monica Y. Lee

AGING CELL(2024)

引用 0|浏览0
暂无评分
摘要
As the innermost lining of the vasculature, endothelial cells (ECs) are constantly subjected to systemic inflammation and particularly vulnerable to aging. Endothelial health is hence vital to prevent age-related vascular disease. Healthy ECs rely on the proper localization of transcription factors via nuclear pore complexes (NPCs) to govern cellular behavior. Emerging studies report NPC degradation with natural aging, suggesting impaired nucleocytoplasmic transport in age-associated EC dysfunction. We herein identify nucleoporin93 (Nup93), a crucial structural NPC protein, as an indispensable player in vascular protection. Endothelial Nup93 protein levels are significantly reduced in the vasculature of aged mice, paralleling observations of Nup93 loss when using in vitro models of EC senescence. The loss of Nup93 in human ECs induces cell senescence and promotes the expression of inflammatory adhesion molecules, where restoring Nup93 protein in senescent ECs reverses features of endothelial aging. Mechanistically, we find that both senescence and loss of Nup93 impair endothelial NPC transport, leading to nuclear accumulation of Yap and downstream inflammation. Pharmacological studies indicate Yap hyperactivation as the primary consequence of senescence and Nup93 loss in ECs. Collectively, our findings indicate that the maintenance of endothelial Nup93 is a key determinant of EC health, where aging targets endothelial Nup93 levels to impair NPC function as a novel mechanism of EC senescence and vascular aging. Endothelial nucleoporin93 (Nup93) is significantly reduced in both the aged vasculature and in primary cell culture senescence models. Suboptimal levels of Nup93 impair nuclear pore transport properties, leading to aberrant nuclear Yap accumulation and endothelial senescence. Loss of Nup93 in human endothelial cells (ECs) induces cellular senescence and inflammation, where restoring Nup93 protein levels is sufficient for endothelial reprogramming toward healthy ECs.image
更多
查看译文
关键词
endothelial cell inflammation,endothelial cell senescence,nuclear pore complex,vascular aging,Yap
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要