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血流切应力改变会导致内皮细胞的质膜损伤。

Altered shear stress of blood flow causes plasma membrane damage in endothelial cells.

作者信息

Raj Nikita, Pan Chang, Starke Ann Marleen, Matos Anna L L, Soehnlein Oliver, Gerke Volker

机构信息

Institute of Medical Biochemistry, Centre for Molecular Biology of Inflammation, University of Münster, Münster, Germany.

Multiscale Imaging Centre, Cells in Motion Interfaculty Center, University of Münster, Münster, Germany.

出版信息

Blood Vessel Thromb Hemost. 2024 Dec 13;2(1):100040. doi: 10.1016/j.bvth.2024.100040. eCollection 2025 Feb.

DOI:10.1016/j.bvth.2024.100040
PMID:40766873
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12320452/
Abstract

The endothelial lining of blood vessels faces many mechanical challenges, including the shear stress (SS) of blood flow, which render it prone to cell membrane ruptures. Such ruptures must be repaired efficiently to maintain cellular integrity and proper vascular function. However, whether SS of blood flow can indeed affect plasma membrane integrity of endothelial cells and whether any ruptures occurring are repaired is not understood. Here, we show that alterations in the SS of fluid flow induce membrane damage in human endothelial cells, and membrane ruptures increase with increasing shear alterations. Furthermore, we show that inherent SS disturbances at aortic branches in mice are associated with endothelial membrane wounds, which are not observed in regions of laminar flow. We also show that endothelial membrane damages inflicted by shear stress alterations are repaired by a Ca-dependent process that involves early endosome exocytosis to provide membrane material for wound closure, suggesting conserved and robust membrane repair responses to endothelial damage in vitro and in vivo. Thus, shear stress alterations, which frequently occur at sites of endothelial dysfunction and before associated pathophysiology, cause membrane wounds in the endothelium, which are repaired efficiently to maintain a functional vasculature.

摘要

血管的内皮衬里面临着许多机械挑战,包括血流的剪切应力(SS),这使其容易发生细胞膜破裂。此类破裂必须得到有效修复,以维持细胞完整性和正常的血管功能。然而,血流的剪切应力是否真的会影响内皮细胞的质膜完整性,以及发生的任何破裂是否会得到修复,目前尚不清楚。在这里,我们表明流体流动剪切应力的改变会导致人内皮细胞的膜损伤,并且膜破裂随着剪切改变的增加而增加。此外,我们表明小鼠主动脉分支处固有的剪切应力紊乱与内皮膜伤口有关,而在层流区域未观察到这种情况。我们还表明,由剪切应力改变造成的内皮膜损伤通过一个依赖钙的过程进行修复,该过程涉及早期内体胞吐作用,以提供用于伤口闭合的膜材料,这表明在体外和体内对内皮损伤存在保守且强大的膜修复反应。因此,剪切应力改变经常发生在内皮功能障碍部位且在相关病理生理学出现之前,它会导致内皮中的膜伤口,这些伤口会得到有效修复以维持功能性脉管系统。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0545/12320452/09353f5acf7b/BVTH_VTH-2024-000190-gr2af.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0545/12320452/802465385621/BVTH_VTH-2024-000190-ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0545/12320452/9241c8dcf8c0/BVTH_VTH-2024-000190-gr1ag.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0545/12320452/09353f5acf7b/BVTH_VTH-2024-000190-gr2af.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0545/12320452/802465385621/BVTH_VTH-2024-000190-ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0545/12320452/9241c8dcf8c0/BVTH_VTH-2024-000190-gr1ag.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0545/12320452/09353f5acf7b/BVTH_VTH-2024-000190-gr2af.jpg

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本文引用的文献

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