| Literature DB >> 27864362 |
Naoto Kajitani1, Kanako Miyano2, Mami Okada-Tsuchioka1, Hiromi Abe1, Kei Itagaki1,3, Kazue Hisaoka-Nakashima4, Norimitsu Morioka4, Yasuhito Uezono2,5, Minoru Takebayashi6,3.
Abstract
Preclinical and clinical evidence suggests that glial cell line-derived neurotrophic factor (GDNF) is important in the therapeutic effect of antidepressants. A previous study demonstrated that the tricyclic antidepressant amitriptyline induces Gαi/o activation, which leads to GDNF expression in astrocytes. However, the specific target expressed in astrocytes that mediates antidepressant-evoked Gαi/o activation has yet to be identified. Thus, the current study explored the possibility that antidepressant-induced Gαi/o activation depends on lysophosphatidic acid receptor 1 (LPAR1), a Gαi/o-coupled receptor. GDNF mRNA expression was examined using real-time PCR and Gαi/o activation was examined using the cell-based receptor assay system CellKeyTM in rat C6 astroglial cells and rat primary cultured astrocytes. LPAR1 antagonists blocked GDNF mRNA expression and Gαi/o activation evoked by various classes of antidepressants (amitriptyline, nortriptyline, mianserin, and fluoxetine). In addition, deletion of LPAR1 by RNAi suppressed amitriptyline-evoked GDNF mRNA expression. Treatment of astroglial cells with the endogenous LPAR agonist LPA increased GDNF mRNA expression through LPAR1, whereas treatment of primary cultured neurons with LPA failed to affect GDNF mRNA expression. Astrocytic GDNF expression evoked by either amitriptyline or LPA utilized, in part, transactivation of fibroblast growth factor receptor and a subsequent ERK cascade. The current results suggest that LPAR1 is a novel, specific target of antidepressants that leads to GDNF expression in astrocytes.Entities:
Keywords: G protein-coupled receptor (GPCR); antidepressants; astrocyte; depression; drug action; glial cell line-derived neurotrophic factor; lipid signaling; lysophosphatidic acid receptor 1; transactivation
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Year: 2016 PMID: 27864362 PMCID: PMC5207162 DOI: 10.1074/jbc.M116.753871
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157