Crawling from soft to stiff matrix polarizes the cytoskeleton and phosphoregulates myosin-II heavy chain

被引:224
|
作者
Raab, Matthew [1 ]
Swift, Joe [1 ]
Dingal, P. C. Dave P. [1 ]
Shah, Palak [1 ]
Shin, Jae-Won [1 ]
Discher, Dennis E. [1 ,2 ]
机构
[1] Univ Penn, Mol & Cell Biophys Lab, Philadelphia, PA 19104 USA
[2] Univ Penn, Cell & Mol Biol Grad Grp, Philadelphia, PA 19104 USA
来源
JOURNAL OF CELL BIOLOGY | 2012年 / 199卷 / 04期
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
MESENCHYMAL STEM-CELLS; DIFFERENTIAL LOCALIZATION; MIGRATING CELLS; SUBSTRATE; PHOSPHORYLATION; 3D; ELASTICITY; MORPHOLOGY; ISOFORMS; RIGIDITY;
D O I
10.1083/jcb.201205056
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
On rigid surfaces, the cytoskeleton of migrating cells is polarized, but tissue matrix is normally soft. We show that nonmuscle MIIB (myosin-IIB) is unpolarized in cells on soft matrix in 2D and also within soft 3D collagen, with rearward polarization of MIIB emerging only as cells migrate from soft to stiff matrix. Durotaxis is the tendency of cells to crawl from soft to stiff matrix, and durotaxis of primary mesenchymal stem cells (MSCs) proved more sensitive to MIIB than to the more abundant and persistently unpolarized nonmuscle MIIA (myosin-IIA). However, MIIA has a key upstream role: in cells on soft matrix, MIIA appeared diffuse and mobile, whereas on stiff matrix, MIIA was strongly assembled in oriented stress fibers that MIIB then polarized. The difference was caused in part by elevated phospho-S1943-MIIA in MSCs on soft matrix, with site-specific mutants revealing the importance of phosphomoderated assembly of MIIA. Polarization is thus shown to be a highly regulated compass for mechanosensitive migration.
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页码:669 / 683
页数:15
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