Antidepressants increase human hippocampal neurogenesis by activating the glucocorticoid receptor

被引:322
作者
Anacker, C. [2 ,3 ,4 ]
Zunszain, P. A.
Cattaneo, A. [5 ]
Carvalho, L. A.
Garabedian, M. J. [6 ]
Thuret, S. [4 ]
Price, J.
Pariante, C. M. [1 ,2 ,3 ]
机构
[1] Kings Coll London, James Black Ctr, Inst Psychiat, Sect Perinatal Psychiat & Stress Psychiat & Immun, London SE5 9NU, England
[2] Natl Inst Hlth Res, Biomed Res Ctr Mental Hlth, Inst Psychiat, London, England
[3] S London & Maudsley NHS Fdn Trust, London, England
[4] Kings Coll London, Inst Psychiat, CCBB, London WC2R 2LS, England
[5] IRCCS San Giovanni Dio, Genet Unit, Brescia, Italy
[6] NYU, Sch Med, Dept Microbiol, New York, NY 10016 USA
基金
英国医学研究理事会;
关键词
adult hippocampal neurogenesis; depression; glucocorticoids; neuroplasticity; stem cells; MESSENGER-RNA EXPRESSION; LONG-TERM TREATMENT; FUNCTION IN-VITRO; CELL-CYCLE EXIT; GENE-EXPRESSION; DIFFERENTIAL REGULATION; NUCLEAR TRANSLOCATION; MAJOR DEPRESSION; PROGENITOR CELLS; BLOOD-CELLS;
D O I
10.1038/mp.2011.26
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
Antidepressants increase adult hippocampal neurogenesis in animal models, but the underlying molecular mechanisms are unknown. In this study, we used human hippocampal progenitor cells to investigate the molecular pathways involved in the antidepressant-induced modulation of neurogenesis. Because our previous studies have shown that antidepressants regulate glucocorticoid receptor (GR) function, we specifically tested whether the GR may be involved in the effects of these drugs on neurogenesis. We found that treatment (for 3-10 days) with the antidepressant, sertraline, increased neuronal differentiation via a GR-dependent mechanism. Specifically, sertraline increased both immature, doublecortin (Dcx)-positive neuroblasts (+16%) and mature, microtubulin-associated protein-2 (MAP2)-positive neurons (+26%). This effect was abolished by the GR-antagonist, RU486. Interestingly, progenitor cell proliferation, as investigated by 5'-bromodeoxyuridine (BrdU) incorporation, was only increased when cells were co-treated with sertraline and the GR-agonist, dexamethasone, (+14%) an effect which was also abolished by RU486. Furthermore, the phosphodiesterase type 4 (PDE4)-inhibitor, rolipram, enhanced the effects of sertraline, whereas the protein kinase A (PKA)-inhibitor, H89, suppressed the effects of sertraline. Indeed, sertraline increased GR transactivation, modified GR phosphorylation and increased expression of the GR-regulated cyclin-dependent kinase-2 (CDK2) inhibitors, p27(Kip1) and p57(Kip2). In conclusion, our data suggest that the antidepressant, sertraline, increases human hippocampal neurogenesis via a GR-dependent mechanism that requires PKA signaling, GR phosphorylation and activation of a specific set of genes. Our data point toward an important role for the GR in the antidepressant-induced modulation of neurogenesis in humans. Molecular Psychiatry (2011) 16, 738-750; doi:10.1038/mp.2011.26; published online 12 April 2011
引用
收藏
页码:738 / 750
页数:13
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