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

被引:5
作者
Bresteau, Enzo [1 ]
Elkhatib, Nadia [1 ]
Baschieri, Francesco [1 ]
Bellec, Karen [1 ,2 ]
Guerin, Melanie [1 ]
Montagnac, Guillaume [1 ]
机构
[1] Univ Paris Saclay, Gustave Roussy Inst, INSERM, U1279, Villejuif, France
[2] Univ Glasgow, Wolfson Wohl Canc Res Ctr, Inst Canc Sci, Glasgow G61 1QH, Lanark, Scotland
关键词
ENDOCYTOSIS; DIMERIZATION; RECRUITMENT; RECEPTORS; CELLS; PITS;
D O I
10.1126/sciadv.abf4647
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页数:11
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