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PMID: 10550057 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Focal adhesion motility revealed in stationary fibroblasts.

Science (New York, N.Y.) ·Vol. 286 ·No. 5442 ·1999-11-05 ·Pages 1172-4

Smilenov LB, Mikhailov A, Pelham RJ, Marcantonio EE, Gundersen GG

Abstract

Focal adhesions (FAs) are clustered integrins and associated proteins that mediate cell adhesion and signaling. A green fluorescent protein-beta1 integrin chimera was used to label FAs in living cells. In stationary cells, FAs were highly motile, moving linearly for several plaque lengths toward the cell center. FA motility was independent of cell density and resulted from contraction of associated actin fibers. In migrating cells, FAs were stationary and only moved in the tail. FA motility in stationary cells suggests that cell movement may be regulated by a clutch-like mechanism by which the affinity of integrins to substrate may be altered in response to migratory cues.

MeSH Terms
3T3 Cells Actins/physiology Animals Cell Adhesion Cell Count Cell Line Cell Movement Fibroblasts/cytology,metabolism Fluorescence Green Fluorescent Proteins Integrin beta1/metabolism Luminescent Proteins Mice Microscopy, Interference Rats Recombinant Fusion Proteins/metabolism
Chemicals
Actins Integrin beta1 Luminescent Proteins Recombinant Fusion Proteins Green Fluorescent Proteins
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Smilenov L B
Department of Pathology, Columbia University, New York, NY 10032, USA.
Mikhailov A
Pelham R J
Marcantonio E E
Gundersen G G
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1999-11-05
Pages
1172-4
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NIGMS NIH HHS · GM42026 · United States
NIGMS NIH HHS · GM44585 · United States
Corrections
CommentIn
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