Cargando…

Comparative Dynamics of Retrograde Actin Flow and Focal Adhesions: Formation of Nascent Adhesions Triggers Transition from Fast to Slow Flow

Dynamic actin network at the leading edge of the cell is linked to the extracellular matrix through focal adhesions (FAs), and at the same time it undergoes retrograde flow with different dynamics in two distinct zones: the lamellipodium (peripheral zone of fast flow), and the lamellum (zone of slow...

Descripción completa

Detalles Bibliográficos
Autores principales: Alexandrova, Antonina Y., Arnold, Katya, Schaub, Sébastien, Vasiliev, Jury M., Meister, Jean-Jacques, Bershadsky, Alexander D., Verkhovsky, Alexander B.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2535565/
https://www.ncbi.nlm.nih.gov/pubmed/18800171
http://dx.doi.org/10.1371/journal.pone.0003234
_version_ 1782159063259283456
author Alexandrova, Antonina Y.
Arnold, Katya
Schaub, Sébastien
Vasiliev, Jury M.
Meister, Jean-Jacques
Bershadsky, Alexander D.
Verkhovsky, Alexander B.
author_facet Alexandrova, Antonina Y.
Arnold, Katya
Schaub, Sébastien
Vasiliev, Jury M.
Meister, Jean-Jacques
Bershadsky, Alexander D.
Verkhovsky, Alexander B.
author_sort Alexandrova, Antonina Y.
collection PubMed
description Dynamic actin network at the leading edge of the cell is linked to the extracellular matrix through focal adhesions (FAs), and at the same time it undergoes retrograde flow with different dynamics in two distinct zones: the lamellipodium (peripheral zone of fast flow), and the lamellum (zone of slow flow located between the lamellipodium and the cell body). Cell migration involves expansion of both the lamellipodium and the lamellum, as well as formation of new FAs, but it is largely unknown how the position of the boundary between the two flow zones is defined, and how FAs and actin flow mutually influence each other. We investigated dynamic relationship between focal adhesions and the boundary between the two flow zones in spreading cells. Nascent FAs first appeared in the lamellipodium. Within seconds after the formation of new FAs, the rate of actin flow decreased locally, and the lamellipodium/lamellum boundary advanced towards the new FAs. Blocking fast actin flow with cytochalasin D resulted in rapid dissolution of nascent FAs. In the absence of FAs (spreading on poly-L-lysine-coated surfaces) retrograde flow was uniform and the velocity transition was not observed. We conclude that formation of FAs depends on actin dynamics, and in its turn, affects the dynamics of actin flow by triggering transition from fast to slow flow. Extension of the cell edge thus proceeds through a cycle of lamellipodium protrusion, formation of new FAs, advance of the lamellum, and protrusion of the lamellipodium from the new base.
format Text
id pubmed-2535565
institution National Center for Biotechnology Information
language English
publishDate 2008
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-25355652008-09-18 Comparative Dynamics of Retrograde Actin Flow and Focal Adhesions: Formation of Nascent Adhesions Triggers Transition from Fast to Slow Flow Alexandrova, Antonina Y. Arnold, Katya Schaub, Sébastien Vasiliev, Jury M. Meister, Jean-Jacques Bershadsky, Alexander D. Verkhovsky, Alexander B. PLoS One Research Article Dynamic actin network at the leading edge of the cell is linked to the extracellular matrix through focal adhesions (FAs), and at the same time it undergoes retrograde flow with different dynamics in two distinct zones: the lamellipodium (peripheral zone of fast flow), and the lamellum (zone of slow flow located between the lamellipodium and the cell body). Cell migration involves expansion of both the lamellipodium and the lamellum, as well as formation of new FAs, but it is largely unknown how the position of the boundary between the two flow zones is defined, and how FAs and actin flow mutually influence each other. We investigated dynamic relationship between focal adhesions and the boundary between the two flow zones in spreading cells. Nascent FAs first appeared in the lamellipodium. Within seconds after the formation of new FAs, the rate of actin flow decreased locally, and the lamellipodium/lamellum boundary advanced towards the new FAs. Blocking fast actin flow with cytochalasin D resulted in rapid dissolution of nascent FAs. In the absence of FAs (spreading on poly-L-lysine-coated surfaces) retrograde flow was uniform and the velocity transition was not observed. We conclude that formation of FAs depends on actin dynamics, and in its turn, affects the dynamics of actin flow by triggering transition from fast to slow flow. Extension of the cell edge thus proceeds through a cycle of lamellipodium protrusion, formation of new FAs, advance of the lamellum, and protrusion of the lamellipodium from the new base. Public Library of Science 2008-09-18 /pmc/articles/PMC2535565/ /pubmed/18800171 http://dx.doi.org/10.1371/journal.pone.0003234 Text en Alexandrova et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Alexandrova, Antonina Y.
Arnold, Katya
Schaub, Sébastien
Vasiliev, Jury M.
Meister, Jean-Jacques
Bershadsky, Alexander D.
Verkhovsky, Alexander B.
Comparative Dynamics of Retrograde Actin Flow and Focal Adhesions: Formation of Nascent Adhesions Triggers Transition from Fast to Slow Flow
title Comparative Dynamics of Retrograde Actin Flow and Focal Adhesions: Formation of Nascent Adhesions Triggers Transition from Fast to Slow Flow
title_full Comparative Dynamics of Retrograde Actin Flow and Focal Adhesions: Formation of Nascent Adhesions Triggers Transition from Fast to Slow Flow
title_fullStr Comparative Dynamics of Retrograde Actin Flow and Focal Adhesions: Formation of Nascent Adhesions Triggers Transition from Fast to Slow Flow
title_full_unstemmed Comparative Dynamics of Retrograde Actin Flow and Focal Adhesions: Formation of Nascent Adhesions Triggers Transition from Fast to Slow Flow
title_short Comparative Dynamics of Retrograde Actin Flow and Focal Adhesions: Formation of Nascent Adhesions Triggers Transition from Fast to Slow Flow
title_sort comparative dynamics of retrograde actin flow and focal adhesions: formation of nascent adhesions triggers transition from fast to slow flow
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2535565/
https://www.ncbi.nlm.nih.gov/pubmed/18800171
http://dx.doi.org/10.1371/journal.pone.0003234
work_keys_str_mv AT alexandrovaantoninay comparativedynamicsofretrogradeactinflowandfocaladhesionsformationofnascentadhesionstriggerstransitionfromfasttoslowflow
AT arnoldkatya comparativedynamicsofretrogradeactinflowandfocaladhesionsformationofnascentadhesionstriggerstransitionfromfasttoslowflow
AT schaubsebastien comparativedynamicsofretrogradeactinflowandfocaladhesionsformationofnascentadhesionstriggerstransitionfromfasttoslowflow
AT vasilievjurym comparativedynamicsofretrogradeactinflowandfocaladhesionsformationofnascentadhesionstriggerstransitionfromfasttoslowflow
AT meisterjeanjacques comparativedynamicsofretrogradeactinflowandfocaladhesionsformationofnascentadhesionstriggerstransitionfromfasttoslowflow
AT bershadskyalexanderd comparativedynamicsofretrogradeactinflowandfocaladhesionsformationofnascentadhesionstriggerstransitionfromfasttoslowflow
AT verkhovskyalexanderb comparativedynamicsofretrogradeactinflowandfocaladhesionsformationofnascentadhesionstriggerstransitionfromfasttoslowflow