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
AUTHORS (6)
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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CITATIONS (145)
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