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αvβ3 integrin associates with activated insulin and PDGFβ receptors and potentiates the biological activity of PDGF
Author(s) -
Schneller Maximilian,
Vuori Kristiina,
Ruoslahti Erkki
Publication year - 1997
Publication title -
the embo journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.484
H-Index - 392
eISSN - 1460-2075
pISSN - 0261-4189
DOI - 10.1093/emboj/16.18.5600
Subject(s) - biology , receptor , integrin , alpha (finance) , platelet derived growth factor receptor , microbiology and biotechnology , insulin receptor , insulin , cancer research , biochemistry , endocrinology , growth factor , insulin resistance , medicine , construct validity , nursing , patient satisfaction
Integrin‐mediated cell attachment modulates growth responses and growth factors regulate cell attachment. Moreover, both cell attachment to extracellular matrix and mitogenic signaling by growth factors are necessary for the proliferation of most types of normal cells, suggesting that integrin and growth factor receptor signaling pathways meet at some downstream point. We report here that a small, highly tyrosine‐phosphorylated fraction of PDGFβ and insulin receptors co‐immunoprecipitates with the αvβ3 integrin from cells. The integrin association requires growth factor stimulation of the receptors. Several signaling molecules that are known to be associated with activated growth factor receptors were present in the αvβ3 integrin complexes. Mitogenicity and chemotaxis induced by PDGF‐BB were enhanced in cells plated on the αvβ3 ligand vitronectin compared with cells plated on the β1 integrin ligand collagen. Thus, the engagement of the αvβ3 integrin in cell–matrix interactions appears to coordinate an intense response to growth factors, helping to explain the importance of this integrin for tissue regeneration, angiogenesis and tumor metastasis.