Molecular clutch drives cell response to surface viscosity

0301 basic medicine Molecular biology Surface Properties Lipid Bilayers Cell Cycle Proteins Microscopy, Atomic Force Cell Line Myoblasts Mice 03 medical and health sciences Animals surface viscosity Cell Shape mechanotransduction Biologia molecular Teixits (Histologia) Adaptor Proteins, Signal Transducing Microscopy Focal Adhesions Viscosity Signal Transducing Adaptor Proteins Atomic Force YAP-Signaling Proteins Phosphoproteins Actins matrix rigidity Extracellular Matrix Fibronectins cell differentiation Tissues Focal Adhesion Kinase 1 Physical Sciences Viscositat Phosphatidylcholines molecular clutch Oligopeptides
DOI: 10.1073/pnas.1710653115 Publication Date: 2018-01-22T20:07:12Z
ABSTRACT
Cell response to matrix rigidity has been explained by the mechanical properties of actin-talin-integrin-fibronectin clutch. Here molecular clutch model is extended account for cell interactions with purely viscous surfaces (i.e., without an elastic component). Supported lipid bilayers present idealized and controllable system through which study this concept. Using lipids different diffusion coefficients, mobility surface viscosity) presented ligands (in case RGD) was altered order magnitude. size cytoskeletal organization were proportional viscosity. Furthermore, there a higher number focal adhesions phosphorylation FAK on less-mobile (more-viscous) surfaces. Actin retrograde flow, indicator force exerted surfaces, also seen be faster more mobile This consequential effects downstream molecules; mechanosensitive YAP protein localized nucleus differentiation myoblast cells enhanced behavior within framework model, lower viscosity leading low loading rate, preventing exposure proteins, causing rate exposing these sites, activating pathways. Consequently, understanding how (regardless stiffness) influences adds further tool engineer materials that control behavior.
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