Abstract
Adhesion and morphogenesis of many non-muscle cells are guided by contractile actomyosin bundles called ventral stress fibers. While it is well established that stress fibers are mechanosensitive structures, physical mechanisms by which they assemble, align, and mature have remained elusive. Here we show that arcs, which serve as precursors for ventral stress fibers, undergo lateral fusion during their centripetal flow to form thick actomyosin bundles that apply tension to focal adhesions at their ends. Importantly, this myosin II-derived force inhibits vectorial actin polymerization at focal adhesions through AMPK-mediated phosphorylation of VASP, and thereby halts stress fiber elongation and ensures their proper contractility. Stress fiber maturation additionally requires ADF/cofilin-mediated disassembly of non-contractile stress fibers, whereas contractile fibers are protected from severing. Taken together, these data reveal that myosin-derived tension precisely controls both actin filament assembly and disassembly to ensure generation and proper alignment of contractile stress fibers in migrating cells.
Highlights
Cell migration is essential for embryonic development, wound healing, immunological processes and cancer metastasis
We show that arc fusion during centripetal flow is accompanied by increased contractility that inhibits vectorial actin polymerization at focal adhesions through AMPKmediated phosphorylation of vasodilator-stimulated phosphoprotein (VASP), insuring formation of ventral stress fibers
While 89% of cells plated on 64 kPa matrix contained ventral stress fibers, only 10% of cells plated on 0.5 kPa matrix exhibited ventral stress fibers as defined by presence of straight, contractile actin bundles connected to focal adhesions at each end
Summary
Cell migration is essential for embryonic development, wound healing, immunological processes and cancer metastasis. Stress fibers guide adhesion, mechanotransduction, endothelial barrier integrity, myofibril assembly, and receptor clustering in T-lymphocytes (Burridge and Wittchen, 2013; Wong et al, 1983; Sanger et al, 2005; Tojkander et al, 2012; Yi et al, 2012) Due to their intrinsic properties, stress fibers have become an important model system for studying the general principles by which contractile actomyosin bundles are assembled in cells. Dorsal (radial) stress fibers are connected to focal adhesions at their distal ends and rise towards the dorsal surface of the cell at their proximal region (Hotulainen and Lappalainen, 2006) They elongate through vectorial actin polymerization at focal adhesions
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