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Cell migration: Fibroblasts find a new way to get ahead
Fibroblasts migrate on two-dimensional (2D) surfaces by forming lamellipodia—actin-rich extensions at the leading edge of the cell that have been well characterized. In this issue, Petrie et al. (2012. J. Cell Biol. http://dx.doi.org/10.1083/jcb.201201124) show that in some 3D environments, includin...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Rockefeller University Press
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3341167/ https://www.ncbi.nlm.nih.gov/pubmed/22547405 http://dx.doi.org/10.1083/jcb.201204039 |
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author | Sixt, Michael |
author_facet | Sixt, Michael |
author_sort | Sixt, Michael |
collection | PubMed |
description | Fibroblasts migrate on two-dimensional (2D) surfaces by forming lamellipodia—actin-rich extensions at the leading edge of the cell that have been well characterized. In this issue, Petrie et al. (2012. J. Cell Biol. http://dx.doi.org/10.1083/jcb.201201124) show that in some 3D environments, including tissue explants, fibroblasts project different structures, termed lobopodia, at the leading edge. Lobopodia still assemble focal adhesions; however, similar to membrane blebs, they are driven by actomyosin contraction and do not accumulate active Rac, Cdc42, and phosphatidylinositol 3-kinases. |
format | Online Article Text |
id | pubmed-3341167 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-33411672012-10-30 Cell migration: Fibroblasts find a new way to get ahead Sixt, Michael J Cell Biol Reviews Fibroblasts migrate on two-dimensional (2D) surfaces by forming lamellipodia—actin-rich extensions at the leading edge of the cell that have been well characterized. In this issue, Petrie et al. (2012. J. Cell Biol. http://dx.doi.org/10.1083/jcb.201201124) show that in some 3D environments, including tissue explants, fibroblasts project different structures, termed lobopodia, at the leading edge. Lobopodia still assemble focal adhesions; however, similar to membrane blebs, they are driven by actomyosin contraction and do not accumulate active Rac, Cdc42, and phosphatidylinositol 3-kinases. The Rockefeller University Press 2012-04-30 /pmc/articles/PMC3341167/ /pubmed/22547405 http://dx.doi.org/10.1083/jcb.201204039 Text en © 2012 Sixt This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Reviews Sixt, Michael Cell migration: Fibroblasts find a new way to get ahead |
title | Cell migration: Fibroblasts find a new way to get ahead |
title_full | Cell migration: Fibroblasts find a new way to get ahead |
title_fullStr | Cell migration: Fibroblasts find a new way to get ahead |
title_full_unstemmed | Cell migration: Fibroblasts find a new way to get ahead |
title_short | Cell migration: Fibroblasts find a new way to get ahead |
title_sort | cell migration: fibroblasts find a new way to get ahead |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3341167/ https://www.ncbi.nlm.nih.gov/pubmed/22547405 http://dx.doi.org/10.1083/jcb.201204039 |
work_keys_str_mv | AT sixtmichael cellmigrationfibroblastsfindanewwaytogetahead |