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周围组织硬度对血管形态发生的生物力学控制

Biomechanical control of vascular morphogenesis by the surrounding stiffness.

作者信息

Hanada Yasuyuki, Halder Semanti, Arima Yuichiro, Haruta Misato, Ogoh Honami, Ogura Shuntaro, Shiraki Yukihiko, Nakano Sota, Ozeki Yuka, Fukuhara Shigetomo, Uemura Akiyoshi, Murohara Toyoaki, Nishiyama Koichi

机构信息

Laboratory for Vascular and Cellular Dynamics, Department of Medical Sciences, University of Miyazaki, Miyazaki, Miyazaki, Japan.

International Research Center for Medical Sciences, Kumamoto University, Kumamoto, Kumamoto, Japan.

出版信息

Nat Commun. 2025 Jul 28;16(1):6788. doi: 10.1038/s41467-025-61804-z.

Abstract

Sprouting angiogenesis is a form of morphogenesis which expands vascular networks from preexisting networks. However, the precise mechanism governing efficient branch elongation driven by directional movement of endothelial cells (ECs), while the lumen develops under the influence of blood inflow, remains unknown. Herein, we show perivascular stiffening to be a major factor that integrates branch elongation and lumen development. The lumen expansion seen during lumen development inhibits directional EC movement driving branch elongation. This process is counter-regulated by the presence of pericytes, which induces perivascular stiffening by promoting the deposition of EC-derived collagen-IV (Col-IV) on the vascular basement membrane (VBM), thereby preventing excessive lumen expansion. Furthermore, inhibition of forward directional movement of the tip EC during lumen development is associated with decreased localization of the F-BAR proteins and Arp2/3 complexes at the leading front. Our results demonstrate how ECs elongate branches, while the lumen develops, by properly building the surrounding physical environment in coordination with pericytes during angiogenesis.

摘要

发芽血管生成是一种形态发生形式,它从预先存在的网络扩展血管网络。然而,在内皮细胞(ECs)定向运动驱动有效分支伸长的精确机制,以及管腔在血流影响下发育的机制,仍然未知。在此,我们表明血管周围硬化是整合分支伸长和管腔发育的主要因素。在管腔发育过程中看到的管腔扩张会抑制驱动分支伸长的ECs定向运动。这个过程受到周细胞的反向调节,周细胞通过促进ECs衍生的IV型胶原(Col-IV)在血管基底膜(VBM)上的沉积来诱导血管周围硬化,从而防止管腔过度扩张。此外,在管腔发育过程中尖端EC向前定向运动的抑制与F-BAR蛋白和Arp2/3复合物在前导前沿的定位减少有关。我们的结果证明了在血管生成过程中,ECs如何通过与周细胞协调构建周围的物理环境来伸长分支,同时管腔发育。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bd4/12304211/e567aff36a2b/41467_2025_61804_Fig1_HTML.jpg

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