A Nodal- and ALK4-independent signaling pathway activated by Cripto-1 through Glypican-1 and c-Src |
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Authors: | Bianco Caterina Strizzi Luigi Rehman Aasia Normanno Nicola Wechselberger Christian Sun Youping Khan Nadia Hirota Morihisa Adkins Heather Williams Kevin Margolis Richard U Sanicola Michele Salomon David S |
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Affiliation: | Mammary Biology and Tumorigenesis Laboratory, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892, USA. |
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Abstract: | Human Cripto-1 (CR-1) is a member of the epidermal growth factor-Cripto FRL1 Cryptic family that has been shown to function as a coreceptor with the type I Activin serine-threonine kinase receptor ALK4 for the transforming growth factor beta-related peptide Nodal. However, CR-1 can also activate the mitogen-activated protein kinase and Akt pathways independently of Nodal and ALK4 by an unknown mechanism. Here, we demonstrate that CR-1 specifically binds to Glypican-1, a membrane-associated heparan sulfate proteoglycan, and activates the tyrosine kinase c-Src, triggering the mitogen-activated protein kinase and Akt signaling pathways. Finally, an active Src kinase is necessary for CR-1 to induce in vitro transformation and migration in mouse mammary epithelial cells. |
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