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The Journal of Neuroscience, May 15, 1999, 19(10):3674-3680
Region-Specific Regulation of RGS4 (Regulator of
G-Protein-Signaling Protein Type 4) in Brain by Stress and
Glucocorticoids: In Vivo and In Vitro
Studies
Yan G.
Ni,
Stephen J.
Gold,
Philip A.
Iredale,
Rose Z.
Terwilliger,
Ronald S.
Duman, and
Eric J.
Nestler
Laboratory of Molecular Psychiatry and Departments of Psychiatry
and Neurobiology, Yale University School of Medicine, New Haven,
Connecticut 06508
The present study demonstrates that the regulator of
G-protein-signaling protein type 4 (RGS4) is differentially regulated in the locus coeruleus (LC) and the paraventricular nucleus
(PVN) of the hypothalamus by chronic stress and glucocorticoid
treatments. Acute or chronic administration of corticosterone to adult
rats decreased RGS4 mRNA levels in the PVN but increased these levels in the LC. Similarly, chronic unpredictable stress decreased RGS4 mRNA
levels in the PVN but had a strong trend to increase these levels in
the LC. Chronic stress also decreased RGS4 mRNA levels in the
pituitary. The molecular mechanisms of RGS4 mRNA regulation were
further investigated in vitro in the LC-like CATH.a cell line and the neuroendocrine AtT20 cell line using the synthetic corticosterone analog dexamethasone. Consistent with the findings in vivo, dexamethasone treatment caused a dose- and
time-dependent decrease in RGS4 mRNA levels in AtT20 cells but a dose-
and time-dependent increase in CATH.a cells. RGS4 mRNA regulation seen
in these two cell lines seems to be attributable, at least in part, to
opposite changes in mRNA stability. The differential regulation of RGS4 expression in the LC and in key relays of the
hypothalamic-pituitary-adrenal axis could contribute to the brain's
region-specific and long-term adaptations to stress.
Key words:
RGS proteins; glucocorticoids; chronic stress; locus
coeruleus; paraventricular nucleus of the hypothalamus; HPA
(hypothalamic-pituitary-adrenal) axis; CATH.a cells; AtT20 cells; cAMP pathway
Copyright © 1999 Society for Neuroscience 0270-6474/99/19103674-07$05.00/0
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