Literature DB >> 12806180

Involvement of vasoactive intestinal peptide on insulin-like growth factor I-induced proliferation of rat pituitary lactotropes in primary culture: evidence for an autocrine and/or paracrine regulatory system.

Miriam Fernández1, Franco Sánchez-Franco, Nuria Palacios, Isabel Sánchez, Gemma Villuendas, Lucinda Cacicedo.   

Abstract

In previous studies we demonstrated that insulin-like growth factor I (IGF-I) induces pituitary vasoactive intestinal peptide (VIP) gene expression and secretion, and that IGF-I-induced prolactin (PRL) release is mediated by VIP. In this study, we investigate the mitotropic action of IGF-I and VIP on pituitary lactotropes, and their possible interplay in this effect. Cultured male rat pituitary cells were treated with rhIGF-I (10(-7)M) and/or VIP (10(-7)M) for 48 h. 5-Bromo-2'-deoxyuridine (BrdU) (10 microM) was added for labeling proliferation of pituitary cells. BrdU-labeling indices indicative of the proliferation rate of lactotropes were determined by double-labeling immunofluorescence staining for PRL and BrdU. Treatment with either IGF-I or VIP increased BrdU-labeling indices of lactotropes, but there was no further increase upon combined incubation with both factors, suggesting an interaction between the signal transduction pathways of IGF-I and VIP. VIP antiserum partially suppressed IGF-I-induced BrdU-labeling indices of lactotropes. We also investigated the intracellular signal transduction pathways in the action of IGF-I and VIP on the proliferation of lactotropes. Treatment of pituitary cells with an inhibitor of the mitogen-activated protein kinase (MAPK) pathway completely abolished IGF-I-induced lactotrope proliferation, whereas it partially suppressed VIP-induced BrdU-labeling indices. The protein kinase A (PKA) inhibitor, which abolished the mitogenic action of VIP, markedly suppressed IGF-I-induced lactotrope proliferation. These results indicate that both IGF-I and VIP stimulate lactotrope proliferation, and that IGF-I-induced lactotrope proliferation is partially mediated by VIP produced locally. Also, this study suggests that interactions between MAPK and cyclic adenosine 3',5'-monophosphate-PKA signaling pathways are implicated in the lactotrope proliferation induced by IGF-I and VIP. Copyright 2003 S. Karger AG, Basel

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Year:  2003        PMID: 12806180     DOI: 10.1159/000070900

Source DB:  PubMed          Journal:  Neuroendocrinology        ISSN: 0028-3835            Impact factor:   4.914


  4 in total

1.  PI3K/Akt/mTOR pathway involvement in regulating growth hormone secretion in a rat pituitary adenoma cell line.

Authors:  Carmelina Di Pasquale; Erica Gentilin; Simona Falletta; Mariaenrica Bellio; Mattia Buratto; Ettore Degli Uberti; Maria Chiara Zatelli
Journal:  Endocrine       Date:  2017-10-27       Impact factor: 3.633

2.  Anterior pituitary adenomas: inherited syndromes, novel genes and molecular pathways.

Authors:  Paraskevi Xekouki; Monalisa Azevedo; Constantine A Stratakis
Journal:  Expert Rev Endocrinol Metab       Date:  2010-09-01

3.  Antagonic effects of oestradiol in interaction with IGF-1 on proliferation of lactotroph cells in vitro.

Authors:  Silvina Gutiérrez; Juan Pablo Petiti; Ana Lucía De Paul; Jorge Humberto Mukdsi; Agustín Aoki; Alicia Inés Torres; Elsa Margarita Orgnero
Journal:  Histochem Cell Biol       Date:  2005-10-28       Impact factor: 4.304

4.  Differential regulation of gonadotropins and glycoprotein hormone alpha-subunit by IGF-I in anterior pituitary cells from male rats.

Authors:  F Pazos; F Sánchez-Franco; J Balsa; J Escalada; L Cacicedo
Journal:  J Endocrinol Invest       Date:  2004 Jul-Aug       Impact factor: 4.256

  4 in total

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