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网格蛋白包被结构通过局部力传递支持三维定向迁移。

Clathrin-coated structures support 3D directed migration through local force transmission.

作者信息

Bresteau Enzo, Elkhatib Nadia, Baschieri Francesco, Bellec Karen, Guérin Mélanie, Montagnac Guillaume

机构信息

Inserm U1279, Gustave Roussy Institute, Université Paris-Saclay, Villejuif, France.

出版信息

Sci Adv. 2021 Nov 5;7(45):eabf4647. doi: 10.1126/sciadv.abf4647.

Abstract

Migrating cells navigate in complex environments through sensing and interpreting biochemical and/or mechanical cues. Here, we report that recently identified tubular clathrin/AP-2 lattices (TCALs), a subset of clathrin-coated structures (CCSs) that pinch collagen fibers, mechanically control directed migration along fibers decorated with ligands of CCS cargoes in three-dimensional (3D) environments. We observed that epidermal growth factor or low-density lipoprotein bound to collagen fibers leads to increased local nucleation and accumulation of TCALs. By using engineered, mixed collagen networks, we demonstrate that this mechanism selectively increases local forces applied on ligand-decorated fibers. We show that these effects depend on the ligand’s receptors but do not rely on their ability to trigger signaling events. We propose that the preferential accumulation of TCALs along ligand-decorated fibers steers migration in 3D environments. We conclude that ligand-regulated, local TCAL accumulation results in asymmetric force distribution that orients cell migration in 3D environments.

摘要

迁移细胞通过感知和解读生化及/或机械信号线索在复杂环境中导航。在此,我们报告,最近发现的管状网格蛋白/衔接蛋白2晶格(TCALs),作为网格蛋白包被结构(CCSs)的一个子集,可夹捏胶原纤维,在三维(3D)环境中沿着装饰有CCSs货物配体的纤维机械性地控制定向迁移。我们观察到,与胶原纤维结合的表皮生长因子或低密度脂蛋白会导致TCALs的局部成核和积累增加。通过使用工程化的混合胶原网络,我们证明这种机制选择性地增加了施加在配体装饰纤维上的局部力。我们表明,这些效应依赖于配体的受体,但不依赖于它们触发信号事件的能力。我们提出,TCALs沿配体装饰纤维的优先积累在3D环境中引导迁移。我们得出结论,配体调节的局部TCAL积累导致不对称力分布,从而使细胞在3D环境中定向迁移。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64b3/8570598/94d0a7e9e358/sciadv.abf4647-f1.jpg

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