4.5 Article

Filamentous network mechanics and active contractility determine cell and tissue shape

期刊

BIOPHYSICAL JOURNAL
卷 95, 期 7, 页码 3488-3496

出版社

BIOPHYSICAL SOC
DOI: 10.1529/biophysj.108.134296

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资金

  1. Emmy Noether program of the German Research Foundation (DFG)
  2. Center for Modelling and Simulation in the Biosciences, Heidelberg, Germany
  3. CellNetworks Cluster of Excellence, Heidelberg, Germany
  4. DFG Research Center for Functional Nanostructures, Karlsruhe, Germany
  5. Karlsruhe Institute of Technology, Germany

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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.

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