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Coordinated collective migration and asymmetric cell division in confluent human keratinocytes without wounding

Epithelial sheet spreading is a fundamental cellular process that must be coordinated with cell division and differentiation to restore tissue integrity. Here we use consecutive serum deprivation and re-stimulation to reconstruct biphasic collective migration and proliferation in cultured sheets of...

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Autores principales: Lång, Emma, Połeć, Anna, Lång, Anna, Valk, Marijke, Blicher, Pernille, Rowe, Alexander D., Tønseth, Kim A., Jackson, Catherine J., Utheim, Tor P., Janssen, Liesbeth M. C., Eriksson, Jens, Bøe, Stig Ove
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6131553/
https://www.ncbi.nlm.nih.gov/pubmed/30202009
http://dx.doi.org/10.1038/s41467-018-05578-7
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author Lång, Emma
Połeć, Anna
Lång, Anna
Valk, Marijke
Blicher, Pernille
Rowe, Alexander D.
Tønseth, Kim A.
Jackson, Catherine J.
Utheim, Tor P.
Janssen, Liesbeth M. C.
Eriksson, Jens
Bøe, Stig Ove
author_facet Lång, Emma
Połeć, Anna
Lång, Anna
Valk, Marijke
Blicher, Pernille
Rowe, Alexander D.
Tønseth, Kim A.
Jackson, Catherine J.
Utheim, Tor P.
Janssen, Liesbeth M. C.
Eriksson, Jens
Bøe, Stig Ove
author_sort Lång, Emma
collection PubMed
description Epithelial sheet spreading is a fundamental cellular process that must be coordinated with cell division and differentiation to restore tissue integrity. Here we use consecutive serum deprivation and re-stimulation to reconstruct biphasic collective migration and proliferation in cultured sheets of human keratinocytes. In this system, a burst of long-range coordinated locomotion is rapidly generated throughout the cell sheet in the absence of wound edges. Migrating cohorts reach correlation lengths of several millimeters and display dependencies on epidermal growth factor receptor-mediated signaling, self-propelled polarized migration, and a G(1)/G(0) cell cycle environment. The migration phase is temporally and spatially aligned with polarized cell divisions characterized by pre-mitotic nuclear migration to the cell front and asymmetric partitioning of nuclear promyelocytic leukemia bodies and lysosomes to opposite daughter cells. This study investigates underlying mechanisms contributing to the stark contrast between cells in a static quiescent state compared to the long-range coordinated collective migration seen in contact with blood serum.
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spelling pubmed-61315532018-09-12 Coordinated collective migration and asymmetric cell division in confluent human keratinocytes without wounding Lång, Emma Połeć, Anna Lång, Anna Valk, Marijke Blicher, Pernille Rowe, Alexander D. Tønseth, Kim A. Jackson, Catherine J. Utheim, Tor P. Janssen, Liesbeth M. C. Eriksson, Jens Bøe, Stig Ove Nat Commun Article Epithelial sheet spreading is a fundamental cellular process that must be coordinated with cell division and differentiation to restore tissue integrity. Here we use consecutive serum deprivation and re-stimulation to reconstruct biphasic collective migration and proliferation in cultured sheets of human keratinocytes. In this system, a burst of long-range coordinated locomotion is rapidly generated throughout the cell sheet in the absence of wound edges. Migrating cohorts reach correlation lengths of several millimeters and display dependencies on epidermal growth factor receptor-mediated signaling, self-propelled polarized migration, and a G(1)/G(0) cell cycle environment. The migration phase is temporally and spatially aligned with polarized cell divisions characterized by pre-mitotic nuclear migration to the cell front and asymmetric partitioning of nuclear promyelocytic leukemia bodies and lysosomes to opposite daughter cells. This study investigates underlying mechanisms contributing to the stark contrast between cells in a static quiescent state compared to the long-range coordinated collective migration seen in contact with blood serum. Nature Publishing Group UK 2018-09-10 /pmc/articles/PMC6131553/ /pubmed/30202009 http://dx.doi.org/10.1038/s41467-018-05578-7 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Lång, Emma
Połeć, Anna
Lång, Anna
Valk, Marijke
Blicher, Pernille
Rowe, Alexander D.
Tønseth, Kim A.
Jackson, Catherine J.
Utheim, Tor P.
Janssen, Liesbeth M. C.
Eriksson, Jens
Bøe, Stig Ove
Coordinated collective migration and asymmetric cell division in confluent human keratinocytes without wounding
title Coordinated collective migration and asymmetric cell division in confluent human keratinocytes without wounding
title_full Coordinated collective migration and asymmetric cell division in confluent human keratinocytes without wounding
title_fullStr Coordinated collective migration and asymmetric cell division in confluent human keratinocytes without wounding
title_full_unstemmed Coordinated collective migration and asymmetric cell division in confluent human keratinocytes without wounding
title_short Coordinated collective migration and asymmetric cell division in confluent human keratinocytes without wounding
title_sort coordinated collective migration and asymmetric cell division in confluent human keratinocytes without wounding
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6131553/
https://www.ncbi.nlm.nih.gov/pubmed/30202009
http://dx.doi.org/10.1038/s41467-018-05578-7
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