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Mitotic cells form actin-based bridges with adjacent cells to provide intercellular communication during rounding
In order to achieve accurate chromosome segregation, eukaryotic cells undergo a dramatic change in morphology to obtain a spherical shape during mitosis. Interphase cells communicate directly with each other by exchanging ions and small molecules via gap junctions, which have important roles in cont...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5105929/ https://www.ncbi.nlm.nih.gov/pubmed/27625181 http://dx.doi.org/10.1080/15384101.2016.1231280 |
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author | Fykerud, Tone A. Knudsen, Lars M. Totland, Max Z. Sørensen, Vigdis Dahal-Koirala, Shiva Lothe, Ragnhild A. Brech, Andreas Leithe, Edward |
author_facet | Fykerud, Tone A. Knudsen, Lars M. Totland, Max Z. Sørensen, Vigdis Dahal-Koirala, Shiva Lothe, Ragnhild A. Brech, Andreas Leithe, Edward |
author_sort | Fykerud, Tone A. |
collection | PubMed |
description | In order to achieve accurate chromosome segregation, eukaryotic cells undergo a dramatic change in morphology to obtain a spherical shape during mitosis. Interphase cells communicate directly with each other by exchanging ions and small molecules via gap junctions, which have important roles in controlling cell growth and differentiation. As cells round up during mitosis, the gap junctional communication between mitotic cells and adjacent interphase cells ceases. Whether mitotic cells use alternative mechanisms for mediating direct cell-cell communication during rounding is currently unknown. Here, we have studied the mechanisms involved in the remodeling of gap junctions during mitosis. We further demonstrate that mitotic cells are able to form actin-based plasma membrane bridges with adjacent cells during rounding. These structures, termed “mitotic nanotubes,” were found to be involved in mediating the transport of cytoplasm, including Rab11-positive vesicles, between mitotic cells and adjacent cells. Moreover, a subpool of the gap-junction channel protein connexin43 localized in these intercellular bridges during mitosis. Collectively, the data provide new insights into the mechanisms involved in the remodeling of gap junctions during mitosis and identify actin-based plasma membrane bridges as a novel means of communication between mitotic cells and adjacent cells during rounding. |
format | Online Article Text |
id | pubmed-5105929 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-51059292016-11-21 Mitotic cells form actin-based bridges with adjacent cells to provide intercellular communication during rounding Fykerud, Tone A. Knudsen, Lars M. Totland, Max Z. Sørensen, Vigdis Dahal-Koirala, Shiva Lothe, Ragnhild A. Brech, Andreas Leithe, Edward Cell Cycle Report In order to achieve accurate chromosome segregation, eukaryotic cells undergo a dramatic change in morphology to obtain a spherical shape during mitosis. Interphase cells communicate directly with each other by exchanging ions and small molecules via gap junctions, which have important roles in controlling cell growth and differentiation. As cells round up during mitosis, the gap junctional communication between mitotic cells and adjacent interphase cells ceases. Whether mitotic cells use alternative mechanisms for mediating direct cell-cell communication during rounding is currently unknown. Here, we have studied the mechanisms involved in the remodeling of gap junctions during mitosis. We further demonstrate that mitotic cells are able to form actin-based plasma membrane bridges with adjacent cells during rounding. These structures, termed “mitotic nanotubes,” were found to be involved in mediating the transport of cytoplasm, including Rab11-positive vesicles, between mitotic cells and adjacent cells. Moreover, a subpool of the gap-junction channel protein connexin43 localized in these intercellular bridges during mitosis. Collectively, the data provide new insights into the mechanisms involved in the remodeling of gap junctions during mitosis and identify actin-based plasma membrane bridges as a novel means of communication between mitotic cells and adjacent cells during rounding. Taylor & Francis 2016-09-13 /pmc/articles/PMC5105929/ /pubmed/27625181 http://dx.doi.org/10.1080/15384101.2016.1231280 Text en © 2016 The Author(s). Published with license by Taylor & Francis http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted. |
spellingShingle | Report Fykerud, Tone A. Knudsen, Lars M. Totland, Max Z. Sørensen, Vigdis Dahal-Koirala, Shiva Lothe, Ragnhild A. Brech, Andreas Leithe, Edward Mitotic cells form actin-based bridges with adjacent cells to provide intercellular communication during rounding |
title | Mitotic cells form actin-based bridges with adjacent cells to provide intercellular communication during rounding |
title_full | Mitotic cells form actin-based bridges with adjacent cells to provide intercellular communication during rounding |
title_fullStr | Mitotic cells form actin-based bridges with adjacent cells to provide intercellular communication during rounding |
title_full_unstemmed | Mitotic cells form actin-based bridges with adjacent cells to provide intercellular communication during rounding |
title_short | Mitotic cells form actin-based bridges with adjacent cells to provide intercellular communication during rounding |
title_sort | mitotic cells form actin-based bridges with adjacent cells to provide intercellular communication during rounding |
topic | Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5105929/ https://www.ncbi.nlm.nih.gov/pubmed/27625181 http://dx.doi.org/10.1080/15384101.2016.1231280 |
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