Mechanism of shape determination in motile cells

被引:573
作者
Keren, Kinneret [1 ,3 ]
Pincus, Zachary [1 ,4 ]
Allen, Greg M. [1 ]
Barnhart, Erin L. [1 ]
Marriott, Gerard [5 ]
Mogilner, Alex [6 ,7 ]
Theriot, Julie A. [1 ,2 ]
机构
[1] Stanford Univ, Sch Med, Dept Biochem, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Microbiol & Immunol, Stanford, CA 94305 USA
[3] Technion Israel Inst Technol, Dept Phys, IL-32000 Haifa, Israel
[4] Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USA
[5] Univ Wisconsin, Dept Physiol, Madison, WI 53706 USA
[6] Univ Calif Davis, Dept Neurobiol Physiol & Behav, Davis, CA 95616 USA
[7] Univ Calif Davis, Dept Math, Davis, CA 95616 USA
关键词
D O I
10.1038/nature06952
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
The shape of motile cells is determined by many dynamic processes spanning several orders of magnitude in space and time, from local polymerization of actin monomers at subsecond timescales to global, cell-scale geometry that may persist for hours. Understanding the mechanism of shape determination in cells has proved to be extremely challenging due to the numerous components involved and the complexity of their interactions. Here we harness the natural phenotypic variability in a large population of motile epithelial keratocytes from fish (Hypsophrys nicaraguensis) to reveal mechanisms of shape determination. We find that the cells inhabit a low-dimensional, highly correlated spectrum of possible functional states. We further show that a model of actin network treadmilling in an inextensible membrane bag can quantitatively recapitulate this spectrum and predict both cell shape and speed. Our model provides a simple biochemical and biophysical basis for the observed morphology and behaviour of motile cells.
引用
收藏
页码:475 / U1
页数:7
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