Filamentous network mechanics and active contractility determine cell and tissue shape

被引:122
作者
Bischofs, Ilka B. [2 ,3 ]
Klein, Franziska [1 ]
Lehnert, Dirk [1 ]
Bastmeyer, Martin [1 ]
Schwarz, Ulrich S. [2 ,4 ]
机构
[1] Univ Karlsruhe TH, Inst Zool Cell & Neurobiol, D-76131 Karlsruhe, Germany
[2] Univ Heidelberg, D-69120 Heidelberg, Germany
[3] Univ Calif Berkeley, Dept Bioengn, Berkeley, CA 94710 USA
[4] Univ Karlsruhe TH, Inst Zool, D-76131 Karlsruhe, Germany
关键词
D O I
10.1529/biophysj.108.134296
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
For both cells and tissues, shape is closely correlated with function presumably via geometry-dependent distribution of tension. In this study, we identify common shape determinants spanning cell and tissue scales. For cells whose sites of adhesion are restricted to small adhesive islands on a micropatterned substrate, shape resembles a sequence of inward-curved circular arcs. The same shape is observed for. broblast-populated collagen gels that are pinned to a. at substrate. Quantitative image analysis reveals that, in both cases, arc radii increase with the spanning distance between the pinning points. Although the Laplace law for interfaces under tension predicts circular arcs, it cannot explain the observed dependence on the spanning distance. Computer simulations and theoretical modeling demonstrate that filamentous network mechanics and contractility give rise to a modified Laplace law that quantitatively explains our experimental findings on both cell and tissue scales. Our model in conjunction with actomyosin inhibition experiments further suggests that cell shape is regulated by two different control modes related to motor contractility and structural changes in the actin cytoskeleton.
引用
收藏
页码:3488 / 3496
页数:9
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