TRANSCRIPTIONAL REGULATION OF HYPOTHALAMIC CORTICOTROPIN-RELEASING FACTOR GENE

被引:12
作者
Kageyama, Kazunori [1 ]
Suda, Toshihiro [1 ]
机构
[1] Hirosaki Univ, Grad Sch Med, Dept Endocrinol & Metab, Aomori, Japan
来源
HORMONES OF THE LIMBIC SYSTEM | 2010年 / 82卷
关键词
CYCLASE-ACTIVATING POLYPEPTIDE; MONOPHOSPHATE-RESPONSIVE ELEMENT; ESTROGEN-RECEPTOR-ALPHA; HORMONE CRH GENE; PARAVENTRICULAR NUCLEUS; RAT HYPOTHALAMUS; 4B CELLS; GLUCOCORTICOID REGULATION; SIGNAL-TRANSDUCTION; EXTENDED AMYGDALA;
D O I
10.1016/S0083-6729(10)82016-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Corticotropin-releasing factor (CRF) plays a central role in regulating stress responses. Forskolin or pituitary adenylate cyclase-activating polypeptide stimulates adenylate cyclase and then increases intracellular cAMP levels in hypothalamic cells. Activation of the protein kinase A pathway leads to binding of cAMP response element (CRE)-binding protein (CREB) on the CRF promoter. Forskolin-stimulated CRF gene transcription is mediated by CRE on the CRF 5'-promoter region. Inducible cAMP-early repressor suppresses a stress response via inhibition of the cAMP-dependent CRF gene. Glucocorticoid-dependent repression of cAMP-stimulated CRF promoter activity is mediated by both nGRE and SRE in hypothalamic cells. Interleukin (IL)-6 produced in the hypothalamus stimulates the CRF gene. Suppressor of cytokine signaling-3, which is induced by a cAMP stimulant and IL-6, is involved in the negative regulation of CRF gene expression in hypothalamic cells. Such complex mechanisms would contribute to stress responses and homeostasis in the hypothalamus. (C) 2010 Elsevier Inc.
引用
收藏
页码:301 / 317
页数:17
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