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10.1038/ncb3246

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C4628555!4628555!26414403
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suck abstract from ncbi


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pmid26414403      Nat+Cell+Biol 2015 ; 17 (11): 1435-45
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  • Competition of two distinct actin networks for actin defines a bistable switch for cell polarization #MMPMID26414403
  • Lomakin AJ; Lee KC; Han SJ; Bui DA; Davidson M; Mogilner A; Danuser G
  • Nat Cell Biol 2015[Nov]; 17 (11): 1435-45 PMID26414403show ga
  • Symmetry-breaking polarization enables functional plasticity of cells and tissues and is yet not well understood. Here we show that epithelial cells, hard-wired to maintain a static morphology and to preserve tissue organization, can spontaneously switch to a migratory polarized phenotype upon relaxation of the actomyosin cytoskeleton. We find that myosin-II engages actin in the formation of cortical actomyosin bundles and thus makes it unavailable for deployment in the process of dendritic growth normally driving cell motility. At low contractility regimes epithelial cells polarize in a front-back manner due to emergence of actin retrograde flows powered by dendritic polymerization of actin. Coupled to cell movement, the flows transport myosin-II from the front to the back of the cell, where the motor locally ?locks? actin in contractile bundles. This polarization mechanism could be employed by embryonic and cancer epithelial cells in microenvironments where high contractility-driven cell motion is inefficient.
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