Vasopressin up-regulates the expression of growth-related immediate-early genes via two distinct EGF receptor transactivation pathways
Abstract
Activation of V1a receptor triggers the expression of growth-related immediate-early genes (IEGs), including c-Fos and Egr-1. We found that pre-treatment of rat vascular smooth muscle A-10 cell line with the EGF receptor inhibitor AG1478 or the over-expression of an EGFR dominant negative mutant (HEBCD533) blocked the vasopressin-induced expression of IEGs, suggesting that activation of these early genes mediated by V1a receptor is via transactivation of the EGF receptor. Importantly, the inhibition of the metalloproteinases, which catalyzed the shedding of the EGF receptor agonist HB-EGF, selectively blocked the vasopressin-induced expression c-Fos. On the other hand, the inhibition of c-Src selectively blocked the vasopressin-induced expression of Egr-1. Interestingly, in contrast to the expression of c-Fos, the expression of Egr-1 was mediated via the Ras/MEK/MAPK-dependent signalling pathway. Vasopressin-triggered expression of both genes required the release of intracellular calcium, activation of PKC and β-arrestin 2. These findings demonstrated that vasopressin up-regulated the expression of c-Fos and Erg-1 via transactivation of two distinct EGF receptor-dependent signalling pathways. © 2008 Elsevier Inc. All rights reserved.
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Título según WOS: | Vasopressin up-regulates the expression of growth-related immediate-early genes via two distinct EGF receptor transactivation pathways |
Título según SCOPUS: | Vasopressin up-regulates the expression of growth-related immediate-early genes via two distinct EGF receptor transactivation pathways |
Título de la Revista: | CELLULAR SIGNALLING |
Volumen: | 20 |
Número: | 9 |
Editorial: | Elsevier Science Inc. |
Fecha de publicación: | 2008 |
Página de inicio: | 1642 |
Página final: | 1650 |
Idioma: | English |
URL: | http://linkinghub.elsevier.com/retrieve/pii/S0898656808001538 |
DOI: |
10.1016/j.cellsig.2008.05.009 |
Notas: | ISI, SCOPUS |