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Smad Proteins are Targets of Transforming Growth Factor β1 in Immortalised Gonadotrophin‐Releasing Hormone Releasing Neurones
Author(s) -
Galbiati M.,
Saredi S.,
Romanò N.,
Martini L.,
Motta M.,
Melcangi R. C.
Publication year - 2005
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.1365-2826.2005.01366.x
Subject(s) - smad , transforming growth factor , medicine , endocrinology , microbiology and biotechnology , phosphorylation , secretion , receptor , chemistry , signal transduction , intracellular , biology , cell culture , genetics
Transforming growth factor β (TGFβ) is one of the growth factors involved in the neuroendocrine control of the gonadotrophin‐releasing hormone (GnRH) neurones. It is produced and released by the astrocytes surrounding GnRH neurones and directly controls their secretory activity. TGFβ signalling is based on a complex of two receptors that transduces the signal through peculiar intracellular substrates, the Smad proteins, which, upon activation, move into the nucleus, and modify the transcription of TGFβ responsive genes. The present study aimed to verify whether TGFβ1 is able to regulate the Smad pathway in GT1‐1 cells (i.e. an immortalised neuronal cell line releasing GnRH). We show that: (i) GT1‐1 cells express Smad 2, 3, 4, and 7; (ii) TGFβ1 enhances the phosphorylation of Smad 2 and 3 at short times of exposure (15–30 min); (iii) TGFβ1 induces the synthesis of the inhibitory Smad 7 at longer times (60–120–240 min); (iv) the conditioned medium of type 1 astrocytes enhances the phosphorylation of Smad 2 and 3 in GT1‐1 cells and a TGFβ1 neutralising antibody counteracts this effect. The results indicate that Smads are targets of TGFβ1 and that astrocytes are able to modulate Smads proteins in GT1‐1 cells through the release of TGFβ1. Taken together, the data provide new evidence that glial cells are important regulators of the GnRH neuronal activity.