Advances in tryptophan hydroxylase-2 gene expression regulation: New insights into serotonin-stress interaction and clinical implications

被引:70
作者
Chen, Guo-Lin [1 ]
Miller, Gregory M. [1 ]
机构
[1] Harvard Univ, Sch Med, New England Primate Res Ctr, Div Neurosci, Southborough, MA 01772 USA
关键词
TPH2; stress response; glucocorticoids; genetics; epigenetics; MESSENGER-RNA EXPRESSION; PITUITARY-ADRENAL AXIS; HUMAN TRYPTOPHAN-HYDROXYLASE-2 GENE; CORTICOTROPIN-RELEASING-FACTOR; BIPOLAR AFFECTIVE-DISORDER; DORSAL-RAPHE NUCLEUS; ATTENTION-DEFICIT/HYPERACTIVITY DISORDER; HYPOTHALAMIC PARAVENTRICULAR NUCLEUS; TISSUE-SPECIFIC EXPRESSION; DEPRESSIVE-LIKE BEHAVIOR;
D O I
10.1002/ajmg.b.32023
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学];
摘要
Serotonin (5-HT) modulates the stress response by interacting with the hormonal hypothalamicpituitaryadrenal (HPA) axis and neuronal sympathetic nervous system (SNS). Tryptophan hydroxylase (TPH) is the rate-limiting enzyme in 5-HT biosynthesis, and the recent identification of a second, neuron-specific TPH isoform (TPH2) opened up a new area of research. While TPH2 genetic variance has been linked to numerous behavioral traits and disorders, findings on TPH2 gene expression have not only reinforced, but also provided new insights into, the long-recognized but not yet fully understood 5-HTstress interaction. In this review, we summarize advances in TPH2 expression regulation and its relevance to the stress response and clinical implications. Particularly, based on findings on rhesus monkey TPH2 genetics and other relevant literature, we propose that: (i) upon activation of adrenal cortisol secretion, the cortisol surge induces TPH2 expression and de novo 5-HT synthesis; (ii) the induced 5-HT in turn inhibits cortisol secretion by modulating the adrenal sensitivity to ACTH via the suprachiasmatic nuclei (SCN)-SNS-adrenal system, such that it contributes to the feedback inhibition of cortisol production; (iii) basal TPH2 expression or 5-HT synthesis, as well as early-life experience, influence basal cortisol primarily via the hormonal HPA axis; and (iv) 5'- and 3'-regulatory polymorphisms of TPH2 may differentially influence the stress response, presumably due to their differential roles in gene expression regulation. Our increasing knowledge of TPH2 expression regulation not only helps us better understand the 5-HTstress interaction and the pathophysiology of neuropsychiatric disorders, but also provides new strategies for the treatment of stress-associated diseases. (C) 2012 Wiley Periodicals, Inc.
引用
收藏
页码:152 / 171
页数:20
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