|  Help  |  About  |  Contact Us

Publication : β1- and αv-class integrins cooperate to regulate myosin II during rigidity sensing of fibronectin-based microenvironments.

First Author  Schiller HB Year  2013
Journal  Nat Cell Biol Volume  15
Issue  6 Pages  625-36
PubMed ID  23708002 Mgi Jnum  J:198991
Mgi Id  MGI:5500089 Doi  10.1038/ncb2747
Citation  Schiller HB, et al. (2013) beta1- and alphav-class integrins cooperate to regulate myosin II during rigidity sensing of fibronectin-based microenvironments. Nat Cell Biol 15(6):625-36
abstractText  How different integrins that bind to the same type of extracellular matrix protein mediate specific functions is unclear. We report the functional analysis of beta1- and alphav-class integrins expressed in pan-integrin-null fibroblasts seeded on fibronectin. Reconstitution with beta1-class integrins promotes myosin-II-independent formation of small peripheral adhesions and cell protrusions, whereas expression of alphav-class integrins induces the formation of large focal adhesions. Co-expression of both integrin classes leads to full myosin activation and traction-force development on stiff fibronectin-coated substrates, with alphav-class integrins accumulating in adhesion areas exposed to high traction forces. Quantitative proteomics linked alphav-class integrins to a GEF-H1-RhoA pathway coupled to the formin mDia1 but not myosin II, and alpha5beta1 integrins to a RhoA-Rock-myosin II pathway. Our study assigns specific functions to distinct fibronectin-binding integrins, demonstrating that alpha5beta1integrins accomplish force generation, whereas alphav-class integrins mediate the structural adaptations to forces, which cooperatively enable cells to sense the rigidity of fibronectin-based microenvironments.
Quick Links:
 
Quick Links:
 

Expression

Publication --> Expression annotations

 

Other

4 Bio Entities

Trail: Publication

0 Expression