Stress and Adrenergic Function: HIF1α, a Potential Regulatory Switch

被引:15
|
作者
Wong, Dona Lee [1 ,2 ]
Tai, T. C. [1 ,2 ,3 ]
Wong-Faull, David C. [1 ]
Claycomb, Robert [1 ]
Siddall, Brenda J. [2 ]
Bell, Rose Ann [2 ]
Kvetnansky, Richard [4 ]
机构
[1] Harvard Univ, Sch Med, Dept Psychiat, Lab Mol & Dev Neurobiol McLean Hosp, Belmont, MA 02478 USA
[2] Stanford Univ, Sch Med, Dept Psychiat & Behav Sci, Nancy Pritzker Lab Dev & Mol Neurobiol, Stanford, CA 94306 USA
[3] Laurentian Univ, Div Med, No Ontario Sch Med, Sudbury, ON P3E 2C6, Canada
[4] Slovak Acad Sci, Inst Expt Endocrinol, Bratislava, Slovakia
关键词
Stress; Phenylethanolamine N-methyltransferase; Transcriptional control; Egr-1; Sp1; HIF1; alpha; PHENYLETHANOLAMINE-N-METHYLTRANSFERASE; TRANSCRIPTION FACTORS SP1; RAT ADRENAL-GLAND; MESSENGER-RNA; GENE-EXPRESSION; HYPOXIA; ACTIVATION; EGR-1; STIMULATION; CELLS;
D O I
10.1007/s10571-010-9567-z
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Stress elicits adrenal epinephrine and cortisol release into the bloodstream to initiate physiological and behavioral responses to counter and overcome stress, the classic "fight or flight" response (Cannon and De La Paz, Am J Physiol 28:64-70, 1911). Stress and the stress hormone epinephrine also contribute to the pathophysiology of illness, e.g., behavioral disorders, cardiovascular disease, and immune dysfunction. Epinephrine itself is regulated by stress through its biosynthesis by phenylethanolamine N-methyltransferase (PNMT, EC 2.1.1.28). Single and repeated immobilization (IMMO) stress in rats stimulates adrenal PNMT mRNA and protein expression via the transcription factors, Egr-1 and Sp1. Moderate hypoxic stress increases PNMT promotor-driven gene expression and endogenous PNMT mRNA and protein in PC12 cells. Induction is initiated through cAMP and PLC signaling, with PKA, PKC, PI3K, ERK1/2 MAPK, and p38 MAPK continuing downstream signal transduction, followed by activation of Egr-1, and Sp1. While functional Egr-1 and Sp1 binding sites exist within the proximal PNMT promoter, a putative hypoxia response element is a weak HIF binding site. Yet, HIF1 alpha overexpression increases PNMT promoter-driven luciferase activity and endogenous PNMT. When the Egr-1 or Sp1 sites are mutated, HIFI a does not stimulate the PNMT promoter. siRNA knock down of Egr-1 or Sp1 prevents promoter activation while siRNA knock down of HIF1 alpha inhibits Egr-1 and Sp1 induction. Findings suggest that hypoxia activates the PNMT gene indirectly via HIF1 alpha stimulation of Egr-1 and Sp1. Thus, for stress-induced illnesses where adrenergic dysfunction is implicated, HIF la may be an "on-off" switch regulating adrenergic responses to stress and a potential target for therapeutic intervention.
引用
收藏
页码:1451 / 1457
页数:7
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