Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.isci.2019.02.002
Title: Spatiotemporally Controlled Myosin Relocalization and Internal Pressure Generate Sibling Cell Size Asymmetry
Authors: Pham, T.T.
Monnard, A.
Helenius, J.
Lund, E.
Lee, N. 
Müller, D.J.
Cabernard, C.
Keywords: Biomechanics
Biophysics
Cell Biology
Methodology in Biological Sciences
Issue Date: 2019
Publisher: Elsevier Inc.
Citation: Pham, T.T., Monnard, A., Helenius, J., Lund, E., Lee, N., Müller, D.J., Cabernard, C. (2019). Spatiotemporally Controlled Myosin Relocalization and Internal Pressure Generate Sibling Cell Size Asymmetry. iScience 13 : Sep-19. ScholarBank@NUS Repository. https://doi.org/10.1016/j.isci.2019.02.002
Rights: Attribution-NonCommercial-NoDerivatives 4.0 International
Abstract: Metazoan cells can generate unequal-sized sibling cells during cell division. This form of asymmetric cell division depends on spindle geometry and Myosin distribution, but the underlying mechanics are unclear. Here, we use atomic force microscopy and live cell imaging to elucidate the biophysical forces involved in the establishment of physical asymmetry in Drosophila neural stem cells. We show that initial apical cortical expansion is driven by hydrostatic pressure, peaking shortly after anaphase onset, and enabled by a relief of actomyosin contractile tension on the apical cell cortex. An increase in contractile tension at the cleavage furrow combined with the relocalization of basally located Myosin initiates basal and sustains apical extension. We propose that spatiotemporally controlled actomyosin contractile tension and hydrostatic pressure enable biased cortical expansion to generate sibling cell size asymmetry. However, dynamic cleavage furrow repositioning can compensate for the lack of biased expansion to establish physical asymmetry. Biomechanics; Biophysics; Cell Biology; Methodology in Biological Sciences © 2019 The Author(s)
Source Title: iScience
URI: https://scholarbank.nus.edu.sg/handle/10635/210792
ISSN: 25890042
DOI: 10.1016/j.isci.2019.02.002
Rights: Attribution-NonCommercial-NoDerivatives 4.0 International
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