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Title: | Comparative dynamics of retrograde actin flow and focal adhesions: Formation of nascent adhesions triggers transition from fast to slow flow | Authors: | Alexandrova A.Y. Arnold K. Schaub S. Vasiliev J.M. Meister J.-J. Bershadsky A.D. Verkhovsky A.B. |
Keywords: | actin cell marker cytochalasin D polylysine animal cell article comparative study controlled study cytoskeleton dissolution dynamics extracellular matrix fibroblast culture focal adhesion lamellipodium melanoma cell microscopy mouse nonhuman phase contrast microscopy rat velocity animal cell motion cell strain 3T3 chemistry experimental melanoma metabolism methodology microfilament 3T3 Cells Actins Animals Cell Movement Cytochalasin D Cytoskeleton Extracellular Matrix Focal Adhesions Melanoma, Experimental Mice Microfilaments Microscopy Microscopy, Phase-Contrast Polylysine Rats |
Issue Date: | 2008 | Citation: | Alexandrova A.Y., Arnold K., Schaub S., Vasiliev J.M., Meister J.-J., Bershadsky A.D., Verkhovsky A.B. (2008). Comparative dynamics of retrograde actin flow and focal adhesions: Formation of nascent adhesions triggers transition from fast to slow flow. PLoS ONE 3 (9) : e3234. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0003234 | Rights: | Attribution 4.0 International | Abstract: | 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. � 2008 Alexandrova et al. | Source Title: | PLoS ONE | URI: | https://scholarbank.nus.edu.sg/handle/10635/161848 | ISSN: | 19326203 | DOI: | 10.1371/journal.pone.0003234 | Rights: | Attribution 4.0 International |
Appears in Collections: | Staff Publications Elements |
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