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Cellular Distribution of G Protein Goa in Pituitary Lactotrophs: Effects of Dopamine
Author(s) -
Painson JeanClaude,
Wenger Tibor,
Lagacé Ginette,
Masson Nicole D.,
Collu Robert
Publication year - 1994
Publication title -
journal of neuroendocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.062
H-Index - 116
eISSN - 1365-2826
pISSN - 0953-8194
DOI - 10.1111/j.1365-2826.1994.tb00606.x
Subject(s) - prolactin cell , medicine , endocrinology , prolactin , cytosol , pertussis toxin , g protein , heterotrimeric g protein , biology , endoplasmic reticulum , anterior pituitary , receptor , pituitary gland , microbiology and biotechnology , signal transduction , chemistry , biochemistry , hormone , enzyme
Membrane‐bound GTP‐binding (G) proteins mediate signal transduction in a variety of cell systems. The exact mechanisms of G proteins action are still under investigation but they appear to involve effectors located in the plasma membrane as well as in other parts of the cell. With this study, we investigated the cellular and ultrastructural localization of G protein subunits, and particularly of Goa, in normal rat anterior pituitaries and in estrone‐induced rat adenomatous lactotrophs. We also evaluated the effects of Goα cellular redistribution in rat adenomatous lactotrophs following short‐term exposure to dopamine (DA). Using the Protein A‐gold (PAG) methodology, Goα was found to be present in the cysternae of the endoplasmic reticulum of normal pituitary cells and of adenomatous lactotrophs. In the latter, Goα could be co‐localized with prolactin (PRL). By immunoblots, using specific antisera, significant amounts of Goα and Gs42α, together with smaller amounts of Giα, Gs47α and Gβ were found to be present in the uncontaminated supernatant fraction of adenomatous lactotrophs. Unexpectedly, exposure of the cells to DA induced a rapid and short‐lived decrease in the cytosolic fraction of Goα and Gβ associated with a decrease of PRL release. Since cytosolic Goα can be ADP‐ribosylated by pertussis toxin (PT) and is therefore in a heterotrimeric form, our data suggest that the soluble Go protein may play a role during lactotrophs' exposure to an inhibitor of PRL release, perhaps through its relocalization after being internalized with the D 2 receptor or by being used for interaction with intracellular and/or membrane‐bound effectors.

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