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Título: | Stimulation of c-Src by prolactin is independent of Jak2 |
Autor: | Fresno Vara, Juan Ángel CSIC; Carretero, María Victoria; Gerónimo, Haydée; Ballmer-Hofer, Kurt; Martín-Pérez, Jorge CSIC ORCID | Palabras clave: | Cytokine signalling Prolactin receptor Proto-oncogenes Tyrosine kinases |
Fecha de publicación: | 1-ene-2000 | Editor: | Biochemical Society | Citación: | Biochemical Journal 345(1): 17-24 (2000) | Resumen: | Interaction of prolactin (PRL) with its receptor (PRLR) leads to activation of Jak and Src family tyrosine kinases. The PRL/growth hormone/cytokine receptor family conserves a proline-rich sequence in the cytoplasmic juxtamembrane region (Box 1) required for association and subsequent activation of Jaks. In the present work, we studied the mechanisms underlying c-Src kinase activation by PRL and the role that Jak2 plays in this process. PRL addition to chicken embryo fibroblasts (CEF) expressing the rat PRLR long form resulted in activation of c-Src and Jak2 and in tyrosine phosphorylation of the receptor. Receptor phosphorylation was due to associated Jak2, since in cells expressing either a Box 1 mutated PRLR (PRLR(4P-A)), which is unable to interact with Jak2, or a kinase-domain-deleted Jak2 (Jak2Deltak), PRL did not stimulate receptor phosphorylation. Interestingly, addition of PRL to cells expressing PRLR(4P-A) resulted in an activation of c-Src equivalent to that observed with the wild-type receptor. These findings indicate that PRL-mediated stimulation of c-Src was independent of Jak2 activation and of receptor phosphorylation. Our results suggest that PRL-activated Src could send signals to downstream cellular targets independently of Jak2. | Descripción: | 8 pages, 5 figures. | Versión del editor: | http://www.biochemj.org/bj/345/bj3450017.htm | URI: | http://hdl.handle.net/10261/24315 | ISSN: | 0264-6021 |
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