Dynamic cytoskeletal regulation of cell shape supports resilience of lymphatic endothelium

细胞骨架 细胞生物学 板层 肌动蛋白 肌动蛋白细胞骨架 化学 淋巴管内皮 生物物理学 生物 淋巴系统 细胞 生物化学 免疫学
作者
Hans Schoofs,Nina Daubel,Sarah Schnabellehner,Max L.B. Grönloh,Sebastián Palacios Martínez,A. Halme,Amanda Marks,Marie Jeansson,Sara Barcos,Cord Brakebusch,Rui Benedito,Britta Engelhardt,Dietmar Vestweber,Konstantin Gaengel,Fabian Linsenmeier,Sebastian Schürmann,Pipsa Saharinen,Jaap D. van Buul,Oliver Friedrich,Richard S. Smith
出处
期刊:Nature [Nature Portfolio]
卷期号:641 (8062): 465-475 被引量:19
标识
DOI:10.1038/s41586-025-08724-6
摘要

Abstract Lymphatic capillaries continuously take up interstitial fluid and adapt to resulting changes in vessel calibre 1–3 . The mechanisms by which the permeable monolayer of loosely connected lymphatic endothelial cells (LECs) 4 maintains mechanical stability remain elusive. Here we identify dynamic cytoskeletal regulation of LEC shape, induced by isotropic stretch, as crucial for the integrity and function of dermal lymphatic capillaries. We found that the oak leaf-shaped LECs showed a spectrum of VE-cadherin-based junctional configurations at the lobular intercellular interface and a unique cytoskeletal organization, with microtubules at concave regions and F-actin at convex lobes. Multispectral and longitudinal intravital imaging of capillary LEC shape and actin revealed dynamic remodelling of cellular overlaps in vivo during homeostasis and in response to interstitial fluid volume increase. Akin to puzzle cells of the plant epidermis 5,6 , LEC shape was controlled by Rho GTPase CDC42-regulated cytoskeletal dynamics, enhancing monolayer stability. Moreover, cyclic isotropic stretch increased cellular overlaps and junction curvature in primary LECs. Our findings indicate that capillary LEC shape results from continuous remodelling of cellular overlaps that maintain vessel integrity while preserving permeable cell–cell contacts compatible with vessel expansion and fluid uptake. We propose a bellows-like fluid propulsion mechanism, in which fluid-induced lumen expansion and shrinkage of LEC overlaps are countered by actin-based lamellipodia-like overlap extension to aid vessel constriction.
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