Modulation of FAK and Src adhesion signaling occurs independently of adhesion complex composition.
J Cell Biol
; 212(3): 349-64, 2016 Feb 01.
Article
em En
| MEDLINE
| ID: mdl-26833789
ABSTRACT
Integrin adhesion complexes (IACs) form mechanochemical connections between the extracellular matrix and actin cytoskeleton and mediate phenotypic responses via posttranslational modifications. Here, we investigate the modularity and robustness of the IAC network to pharmacological perturbation of the key IAC signaling components focal adhesion kinase (FAK) and Src. FAK inhibition using AZ13256675 blocked FAK(Y397) phosphorylation but did not alter IAC composition, as reported by mass spectrometry. IAC composition was also insensitive to Src inhibition using AZD0530 alone or in combination with FAK inhibition. In contrast, kinase inhibition substantially reduced phosphorylation within IACs, cell migration and proliferation. Furthermore using fluorescence recovery after photobleaching, we found that FAK inhibition increased the exchange rate of a phosphotyrosine (pY) reporter (dSH2) at IACs. These data demonstrate that kinase-dependent signal propagation through IACs is independent of gross changes in IAC composition. Together, these findings demonstrate a general separation between the composition of IACs and their ability to relay pY-dependent signals.
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Transdução de Sinais
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Adesão Celular
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Quinases da Família src
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Adesões Focais
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Quinase 1 de Adesão Focal
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Fibroblastos
Limite:
Animals
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Humans
Idioma:
En
Revista:
J Cell Biol
Ano de publicação:
2016
Tipo de documento:
Article
País de afiliação:
Reino Unido