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Cited by 317

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

c-Src enhances the spreading of src-/- fibroblasts on fibronectin by a kinase-independent mechanism.

Open access
Kaplan, K B, Swedlow, J R, Morgan, D O, Varmus, H E·1995·Genes & Development

Abstract

We have explored the role of the tyrosine kinase c-Src in cellular adhesion. Fibroblasts derived from src-/- mice (src-/- fibroblasts) exhibit a reduced rate of spreading on fibronectin. These defect is rescued by expression of wild-type chicken c-Src. Analyses of mutants suggest that c-Src increases the rate of cell spreading in src-/- fibroblasts through a kinase-independent mechanism requiring both the SH3 and SH2 domains. To further address the role of c-Src in adhesion, we examined the activity and subcellular distribution of c-Src during the adhesion of fibroblasts on fibronectin. We observed a transient increase in the specific kinase activity of c-Src accompanied by the partial dephosphorylation of the negative regulatory site Y527. Activation of c-Src is followed by its redistribution to newly formed focal adhesions. These results suggest that the enzymatic activity and subcellular distribution of c-Src are coordinately regulated during cellular adhesion and that c-Src can affect adhesion by a kinase-independent mechanism.

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Metadata

Authors
Kaplan, K. B., Swedlow, J. R., Morgan, D. O., & Varmus, H. E.
Venue
Genes & Development
Published
1995-06-15
Volume
9
Issue
12
Pages
1505-1517
ISSN
  • 0890-9369 (ISSN-L)
  • 1549-5477
OpenAlex
W1982849870
Cited by
317
References
1
Type
posted content
Language
en
Open access
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CoChat. (2026). Citation check: c-Src enhances the spreading of src-/- fibroblasts on fibronectin by a kinase-independent mechanism. https://app.cochat.ai/papers/10.1101/gad.9.12.1505
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Kaplan, K. B., Swedlow, J. R., Morgan, D. O., & Varmus, H. E. (1995). c-Src enhances the spreading of src-/- fibroblasts on fibronectin by a kinase-independent mechanism. Genes & Development. https://doi.org/10.1101/gad.9.12.1505

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