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Multiple cAMP-induced signaling cascades regulate prolactin expression in T cells

par Gerlo, Sarah;Verdood, Peggy;Peters, Elisabeth ;Kooijman, Ron
Référence Cellular and molecular life sciences, 63, 1, page (92-99)
Publication Publié, 2006-01

Article révisé par les pairs

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Résumé :

Beside its pivotal role in reproduction, the pituitary hormone prolactin (PRL) has been attributed an immunomodulatory function. Here we report that cAMP is an important stimulator of PRL transcription in primary human T lymphocytes. Inhibition of both protein kinase A (PKA) and p38 MAPK partially abrogated cAMP-induced PRL expression. In addition, cAMP-induced phosphorylation of p38 was shown to occur independently of PKA and could be mimicked by a methylated cAMP analogue which specifically activates the recently discovered cAMP receptor EPAC (exchange protein directly activated by cAMP). Our findings suggest that cAMP induces PRL expression in T lymphocytes via cooperation of at least two different signaling pathways: a PKA-dependent pathway leading to the phosphorylation of cAMP response element-binding protein, and a PKA-independent pathway leading to p38 phosphorylation. © Birkhäuser Verlag, 2006.