TY - JOUR
T1 - Clathrin-coated structures support 3D directed migration through local force transmission
AU - Bresteau, Enzo
AU - Elkhatib, Nadia
AU - Baschieri, Francesco
AU - Bellec, Karen
AU - Guérin, Mélanie
AU - Montagnac, Guillaume
N1 - Publisher Copyright:
Copyright © 2021 The Authors, some rights reserved;
PY - 2021/11/1
Y1 - 2021/11/1
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85118627383&partnerID=8YFLogxK
U2 - 10.1126/sciadv.abf4647
DO - 10.1126/sciadv.abf4647
M3 - Article
C2 - 34739323
AN - SCOPUS:85118627383
SN - 2375-2548
VL - 7
JO - Science Advances
JF - Science Advances
IS - 45
M1 - eabf4647
ER -