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Anti-proliferative effects and cell death mediated by two isoforms of dopamine D2 receptors in pituitary tumor cells

Authors
 Juan Ji An  ;  Sang-Rae Cho  ;  Ja-Hyun Baik  ;  Young Soo Ahn  ;  Kye Won Park  ;  Dae Won Jeong 
Citation
 MOLECULES AND CELLS, Vol.206(1-2) : 49-62, 2003 
Journal Title
 MOLECULES AND CELLS 
ISSN
 1016-8478 
Issue Date
2003
MeSH
Animals ; Apoptosis/drug effects* ; Cell Division/drug effects ; Cell Line, Tumor ; Dopamine/pharmacology ; Dopamine Agonists/pharmacology ; Dopamine Antagonists/pharmacology ; Mitogen-Activated Protein Kinase 3 ; Mitogen-Activated Protein Kinases/metabolism ; Pituitary Neoplasms/pathology* ; Protein Isoforms/physiology ; Rats ; Receptors, Dopamine D2/metabolism ; Receptors, Dopamine D2/physiology* ; Signal Transduction ; p38 Mitogen-Activated Protein Kinases
Keywords
Anti-proliferative effects ; Dopamine D2 receptor ; Pituitary tumor cells
Abstract
Stable rat pituitary tumor cell lines expressing two isoforms of the dopamine D2 receptor, D2L (long) and D2S (short) (the GH3D2L and GH3D2S cell lines, respectively), were established, and the signaling pathway underlying the anti-proliferative and cell death effects of dopaminergic agonists was examined in these cells. After either dopamine or quinpirole treatment, the cell viability decreased significantly only in GH3D2L cells and GH3D2S cells, but not in GH3 cells where D2 receptors are absent. Treatment with haloperidol, a specific D2 receptor antagonist, rescued the dopamine-mediated decreased cell viability in both the GH3D2L and GH3D2S cells. Treatment of these cells with dopamine decreased the DNA synthesis rate, as demonstrated by the incorporation of 5-bromo-2′-deoxyuridine (BrdU). Dopamine-induced cell death was observed in the GH3D2L and GH3D2S cells, and was accompanied by DNA laddering and caspase-3 activation, which were blunted by haloperidol, indicating that dopamine-induced cell death in these cells is mediated by the dopamine D2 receptors. D2 receptor-mediated cell death in these cells correlated with the sustained and enhanced activation of p38 mitogen-activated protein kinase (MAPK) and the extracellular-signal regulated kinase (ERK)1/2 pathways. Treatment with SB203580, which is a specific p38 MAPK inhibitor and PD98059, which is an inhibitor of MEK1/ERK signaling, selectively abrogates dopamine-induced cell death. It was further shown that p38 MAPK and ERK activation was inhibited by the antioxidant, N-acetylcysteine (NAC), and that a treatment with haloperidol completely blocked the p38 and ERK activation induced by dopamine. These results suggest that dopamine induces an anti-proliferative effect and cell death via the dopamine D2 receptors, by means of the p38 MAPK and ERK pathways involving oxidative stress, in the pituitary tumor cells.
Full Text
http://www.sciencedirect.com/science/article/pii/S0303720703002363
DOI
10.1016/S0303-7207(03)00236-3
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pharmacology (약리학교실) > 1. Journal Papers
Yonsei Authors
Ahn, Young Soo(안영수)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/114246
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