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Focal adhesions control cleavage furrow shape and spindle tilt during mitosis

The geometry of the cleavage furrow during mitosis is often asymmetric in vivo and plays a critical role in stem cell differentiation and the relative positioning of daughter cells during development. Early observations of adhesive cell lines revealed asymmetry in the shape of the cleavage furrow, w...

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Autores principales: Taneja, Nilay, Fenix, Aidan M., Rathbun, Lindsay, Millis, Bryan A., Tyska, Matthew J., Hehnly, Heidi, Burnette, Dylan T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4949487/
https://www.ncbi.nlm.nih.gov/pubmed/27432211
http://dx.doi.org/10.1038/srep29846
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author Taneja, Nilay
Fenix, Aidan M.
Rathbun, Lindsay
Millis, Bryan A.
Tyska, Matthew J.
Hehnly, Heidi
Burnette, Dylan T.
author_facet Taneja, Nilay
Fenix, Aidan M.
Rathbun, Lindsay
Millis, Bryan A.
Tyska, Matthew J.
Hehnly, Heidi
Burnette, Dylan T.
author_sort Taneja, Nilay
collection PubMed
description The geometry of the cleavage furrow during mitosis is often asymmetric in vivo and plays a critical role in stem cell differentiation and the relative positioning of daughter cells during development. Early observations of adhesive cell lines revealed asymmetry in the shape of the cleavage furrow, where the bottom (i.e., substrate attached side) of the cleavage furrow ingressed less than the top (i.e., unattached side). This data suggested substrate attachment could be regulating furrow ingression. Here we report a population of mitotic focal adhesions (FAs) controls the symmetry of the cleavage furrow. In single HeLa cells, stronger adhesion to the substrate directed less ingression from the bottom of the cell through a pathway including paxillin, focal adhesion kinase (FAK) and vinculin. Cell-cell contacts also direct ingression of the cleavage furrow in coordination with FAs in epithelial cells—MDCK—within monolayers and polarized cysts. In addition, mitotic FAs established 3D orientation of the mitotic spindle and the relative positioning of mother and daughter centrosomes. Therefore, our data reveals mitotic FAs as a key link between mitotic cell shape and spindle orientation, and may have important implications in our understanding stem cell homeostasis and tumorigenesis.
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spelling pubmed-49494872016-07-26 Focal adhesions control cleavage furrow shape and spindle tilt during mitosis Taneja, Nilay Fenix, Aidan M. Rathbun, Lindsay Millis, Bryan A. Tyska, Matthew J. Hehnly, Heidi Burnette, Dylan T. Sci Rep Article The geometry of the cleavage furrow during mitosis is often asymmetric in vivo and plays a critical role in stem cell differentiation and the relative positioning of daughter cells during development. Early observations of adhesive cell lines revealed asymmetry in the shape of the cleavage furrow, where the bottom (i.e., substrate attached side) of the cleavage furrow ingressed less than the top (i.e., unattached side). This data suggested substrate attachment could be regulating furrow ingression. Here we report a population of mitotic focal adhesions (FAs) controls the symmetry of the cleavage furrow. In single HeLa cells, stronger adhesion to the substrate directed less ingression from the bottom of the cell through a pathway including paxillin, focal adhesion kinase (FAK) and vinculin. Cell-cell contacts also direct ingression of the cleavage furrow in coordination with FAs in epithelial cells—MDCK—within monolayers and polarized cysts. In addition, mitotic FAs established 3D orientation of the mitotic spindle and the relative positioning of mother and daughter centrosomes. Therefore, our data reveals mitotic FAs as a key link between mitotic cell shape and spindle orientation, and may have important implications in our understanding stem cell homeostasis and tumorigenesis. Nature Publishing Group 2016-07-19 /pmc/articles/PMC4949487/ /pubmed/27432211 http://dx.doi.org/10.1038/srep29846 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Taneja, Nilay
Fenix, Aidan M.
Rathbun, Lindsay
Millis, Bryan A.
Tyska, Matthew J.
Hehnly, Heidi
Burnette, Dylan T.
Focal adhesions control cleavage furrow shape and spindle tilt during mitosis
title Focal adhesions control cleavage furrow shape and spindle tilt during mitosis
title_full Focal adhesions control cleavage furrow shape and spindle tilt during mitosis
title_fullStr Focal adhesions control cleavage furrow shape and spindle tilt during mitosis
title_full_unstemmed Focal adhesions control cleavage furrow shape and spindle tilt during mitosis
title_short Focal adhesions control cleavage furrow shape and spindle tilt during mitosis
title_sort focal adhesions control cleavage furrow shape and spindle tilt during mitosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4949487/
https://www.ncbi.nlm.nih.gov/pubmed/27432211
http://dx.doi.org/10.1038/srep29846
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