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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...

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Autores principales: Hu, Shiqiong, Planus, Emmanuelle, Georgess, Dan, Place, Christophe, Wang, Xianghui, Albiges-Rizo, Corinne, Jurdic, Pierre, Géminard, Jean-Christophe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2011
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.
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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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