Journal
BIOPHYSICAL JOURNAL
Volume 99, Issue 11, Pages 3526-3534Publisher
CELL PRESS
DOI: 10.1016/j.bpj.2010.10.006
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Funding
- National Institutes of Health [GM084204, CA143868, EB008259]
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Upon cortical retraction in mitosis mammalian cells have a dramatically decreased physical association with their environment Hence mechanisms that prevent mitotic detachment and ensure appropriate positioning of the resulting daughter cells are critical for effective tissue morphogenesis and repair and are the subject of this study We find that unlike low motility cells highly motile cells spread isotropically upon division and do not typically reoccupy their mother cell footprint and often even disseminate their mitotic cells To elucidate these different motility based phenotypes we investigated their partial recapitulation and rescue using defined molecular perturbations We show that activated RhoA is localized at the mitotic cell cortex and Rho associated kinase inhibition increases the degree of reoccupation of the mother cell outline in highly motile cells Conversely we show that induction of motility in low motility cells by RasV12 overexpression results in increased isotropic daughter cell spreading We thus propose that a balance between cortical retraction forces which depend in part on RhoA activation and substrate adhesion forces which diminish with increasing motility rates governs the integrity of mitotic actin retraction fibers and influences subsequent daughter cell spreading This balance of forces during mitosis has implications for cancer metastasis
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