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Podosome rings generate forces that drive saltatory osteoclast migration
Podosomes are dynamic, actin-containing adhesion structures that collectively self-organize as rings. In this study, we first show by observing osteoclasts plated on bead-seeded soft substrates that podosome assemblies, such as rings, are involved in tension forces. During the expansion of a podosom...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3164459/ https://www.ncbi.nlm.nih.gov/pubmed/21737683 http://dx.doi.org/10.1091/mbc.E11-01-0086 |
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author | Hu, Shiqiong Planus, Emmanuelle Georgess, Dan Place, Christophe Wang, Xianghui Albiges-Rizo, Corinne Jurdic, Pierre Géminard, Jean-Christophe |
author_facet | Hu, Shiqiong Planus, Emmanuelle Georgess, Dan Place, Christophe Wang, Xianghui Albiges-Rizo, Corinne Jurdic, Pierre Géminard, Jean-Christophe |
author_sort | Hu, Shiqiong |
collection | PubMed |
description | Podosomes are dynamic, actin-containing adhesion structures that collectively self-organize as rings. In this study, we first show by observing osteoclasts plated on bead-seeded soft substrates that podosome assemblies, such as rings, are involved in tension forces. During the expansion of a podosome ring, substrate displacement is oriented outward, suggesting that podosomal structures push the substrate away. To further elucidate the function of forces generated by podosomes, we analyze osteoclast migration. Determining the centers of mass of the whole cell (G) and of actin (P), we demonstrate that osteoclasts migrate by “jumps” and that the trajectories of G and P are strongly correlated. The velocity of the center of mass as a function of time reveals that osteoclasts rapidly catch up with podosomal structures in a periodic pattern. We conclude that actin dynamics inside the cell are not only correlated with cell migration, but drive it. |
format | Online Article Text |
id | pubmed-3164459 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-31644592011-11-16 Podosome rings generate forces that drive saltatory osteoclast migration Hu, Shiqiong Planus, Emmanuelle Georgess, Dan Place, Christophe Wang, Xianghui Albiges-Rizo, Corinne Jurdic, Pierre Géminard, Jean-Christophe Mol Biol Cell Articles Podosomes are dynamic, actin-containing adhesion structures that collectively self-organize as rings. In this study, we first show by observing osteoclasts plated on bead-seeded soft substrates that podosome assemblies, such as rings, are involved in tension forces. During the expansion of a podosome ring, substrate displacement is oriented outward, suggesting that podosomal structures push the substrate away. To further elucidate the function of forces generated by podosomes, we analyze osteoclast migration. Determining the centers of mass of the whole cell (G) and of actin (P), we demonstrate that osteoclasts migrate by “jumps” and that the trajectories of G and P are strongly correlated. The velocity of the center of mass as a function of time reveals that osteoclasts rapidly catch up with podosomal structures in a periodic pattern. We conclude that actin dynamics inside the cell are not only correlated with cell migration, but drive it. The American Society for Cell Biology 2011-09-01 /pmc/articles/PMC3164459/ /pubmed/21737683 http://dx.doi.org/10.1091/mbc.E11-01-0086 Text en © 2011 Hu et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society of Cell Biology. |
spellingShingle | Articles Hu, Shiqiong Planus, Emmanuelle Georgess, Dan Place, Christophe Wang, Xianghui Albiges-Rizo, Corinne Jurdic, Pierre Géminard, Jean-Christophe Podosome rings generate forces that drive saltatory osteoclast migration |
title | Podosome rings generate forces that drive saltatory osteoclast migration |
title_full | Podosome rings generate forces that drive saltatory osteoclast migration |
title_fullStr | Podosome rings generate forces that drive saltatory osteoclast migration |
title_full_unstemmed | Podosome rings generate forces that drive saltatory osteoclast migration |
title_short | Podosome rings generate forces that drive saltatory osteoclast migration |
title_sort | podosome rings generate forces that drive saltatory osteoclast migration |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3164459/ https://www.ncbi.nlm.nih.gov/pubmed/21737683 http://dx.doi.org/10.1091/mbc.E11-01-0086 |
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