Blebs are spherical membrane protrusions often observed during cell migration, cell spreading, cytokinesis, and apoptosis, both in cultured cells and in vivo. Bleb expansion is thought to be driven by the contractile actomyosin cortex, which generates hydrostatic pressure in the cytoplasm and can thus drive herniations of the plasma membrane. However, the role of cortical tension in bleb formation has not been directly tested, and despite the importance of blebbing, little is known about the mechanisms of bleb growth. In order to explore the link between cortical tension and bleb expansion, we induced bleb formation on cells with different tensions. Blebs were nucleated in a controlled manner by laser ablation of the cortex, mimicking endogenous bleb nucleation. Cortical tension was modified by treatments affecting the level of myosin activity or proteins regulating actin turnover. We show that there is a critical tension below which blebs cannot expand. Above this threshold, the maximal size of a bleb strongly depends on tension, and this dependence can be fitted with a model of the cortex as an active elastic material. Together, our observations and model allow us to relate bleb shape parameters to the underlying cellular mechanics and provide insights as to how bleb formation can be biochemically regulated during cell motility.
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London Ctr Nanotechnol, London WC1H 0AH, England
UCL, Dept Cell & Dev Biol, Fac Life Sci, London, EnglandLondon Ctr Nanotechnol, London WC1H 0AH, England
Charras, Guillaume
;
Paluch, Ewa
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Max Planck Inst Cell Biol & Genet, D-01307 Dresden, Germany
Int Inst Mol & Cell Biol, PL-02109 Warsaw, PolandLondon Ctr Nanotechnol, London WC1H 0AH, England
机构:
UCL, Dept Physiol, London, England
Harvard Univ, Sch Med, Dept Syst Biol, Boston, MA USAUCL, Dept Physiol, London, England
Charras, Guillaume T.
;
Coughlin, Margaret
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Harvard Univ, Sch Med, Dept Syst Biol, Boston, MA USAUCL, Dept Physiol, London, England
Coughlin, Margaret
;
Mitchison, Timothy J.
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Harvard Univ, Sch Med, Dept Syst Biol, Boston, MA USAUCL, Dept Physiol, London, England
Mitchison, Timothy J.
;
Mahadevan, L.
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Harvard Univ, Sch Med, Dept Syst Biol, Boston, MA USA
Harvard Univ, Sch Engn & Appl Sci, Cambridge, MA USA
Harvard Univ, Dept Organ & Evolut Biol, Cambridge, MA USAUCL, Dept Physiol, London, England
机构:
London Ctr Nanotechnol, London WC1H 0AH, England
UCL, Dept Cell & Dev Biol, Fac Life Sci, London, EnglandLondon Ctr Nanotechnol, London WC1H 0AH, England
Charras, Guillaume
;
Paluch, Ewa
论文数: 0引用数: 0
h-index: 0
机构:
Max Planck Inst Cell Biol & Genet, D-01307 Dresden, Germany
Int Inst Mol & Cell Biol, PL-02109 Warsaw, PolandLondon Ctr Nanotechnol, London WC1H 0AH, England
机构:
UCL, Dept Physiol, London, England
Harvard Univ, Sch Med, Dept Syst Biol, Boston, MA USAUCL, Dept Physiol, London, England
Charras, Guillaume T.
;
Coughlin, Margaret
论文数: 0引用数: 0
h-index: 0
机构:
Harvard Univ, Sch Med, Dept Syst Biol, Boston, MA USAUCL, Dept Physiol, London, England
Coughlin, Margaret
;
Mitchison, Timothy J.
论文数: 0引用数: 0
h-index: 0
机构:
Harvard Univ, Sch Med, Dept Syst Biol, Boston, MA USAUCL, Dept Physiol, London, England
Mitchison, Timothy J.
;
Mahadevan, L.
论文数: 0引用数: 0
h-index: 0
机构:
Harvard Univ, Sch Med, Dept Syst Biol, Boston, MA USA
Harvard Univ, Sch Engn & Appl Sci, Cambridge, MA USA
Harvard Univ, Dept Organ & Evolut Biol, Cambridge, MA USAUCL, Dept Physiol, London, England