Directional control of lamellipodia extension by constraining cell shape and orienting cell tractional forces

被引:358
作者
Parker, KK
Brock, AL
Brangwynne, C
Mannix, RJ
Wang, N
Ostuni, E
Geisse, NA
Adams, JC
Whitesides, GM
Ingber, DE
机构
[1] Harvard Univ, Sch Med, Childrens Hosp, Dept Surg, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Childrens Hosp, Dept Pathol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Publ Hlth, Physiol Program, Boston, MA 02115 USA
[4] Harvard Univ, Dept Chem & Biol Chem, Cambridge, MA 02138 USA
[5] Boston Univ, Dept Phys, Boston, MA 02215 USA
[6] MRC, Mol Cell Biol Lab, London, England
[7] UCL, Dept Biochem & Mol Biol, London, England
关键词
migration; motility; focal adhesion; cell tension; microspike; microcontact printing;
D O I
10.1096/fj.02-0038com
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Directed cell migration is critical for tissue morphogenesis and wound healing, but the mechanism of directional control is poorly understood. Here we show that the direction in which cells extend their leading edge can be controlled by constraining cell shape using micrometer-sized extracellular matrix (ECM) islands. When cultured on square ECM islands in the presence of motility factors, cells preferentially extended lamellipodia, filopodia, and microspikes from their corners. Square cells reoriented their stress fibers and focal adhesions so that tractional forces were concentrated in these corner regions. When cell tension was dissipated, lamellipodia extension ceased. Mechanical interactions between cells and ECM that modulate cytoskeletal tension may therefore play a key role in the control of directional cell motility.
引用
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页码:1195 / 1204
页数:10
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