Corticosterone actions on the hippocampal brain-derived neurotrophic factor expression are mediated by exon IV promoter

被引:83
作者
Hansson, AC
Sommer, WH
Metsis, M
Strömberg, I
Agnati, LF
Fuxe, K
机构
[1] NIAAA, NIH, Clin Sci Lab, Bethesda, MD 20892 USA
[2] Karolinska Inst, Dept Neurosci, Stockholm, Sweden
[3] Karolinska Inst, Dept Biochem & Biophys, Stockholm, Sweden
[4] Umea Univ, Dept Integrat Med Biol, Umea, Sweden
[5] Univ Modena, Dept Biomed Sci, I-41100 Modena, Italy
基金
日本科学技术振兴机构;
关键词
neurotrophin; brain-derived neurotrophic factor; adrenalectomy; glucocorticoids; rat brain neurotrophin; rat brain;
D O I
10.1111/j.1365-2826.2005.01390.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Brain-derived neurotrophic factor (BDNF) expression is strongly regulated by adrenocorticosteroids via activated gluco- and mineralocorticoid receptors. Four separate promoters are located upstream of the BDNF noncoding exons I to IV and may thus be involved in adrenocorticosteroid-mediated gene regulation. In adrenalectomised rats, corticosterone (10 mg/kg s.c.) induces a robust down-regulation of both BDNF mRNA and protein levels in the hippocampus peaking at 2-8 h. To study the role of the individual promoters in the corticosterone response, we employed exon-specific riboprobe in situ hybridisation as well as real-time polymerase chain reaction (PCR) in the dentate gyrus. We found a down-regulation, mainly of exon IV and the protein-coding exon V, in nearby all hippocampal subregions, but exon II was only down-regulated in the dentate gyrus. Exon I and exon III transcripts were not affected by corticosterone treatment. The results could be confirmed with real-time PCR in the dentate gyrus. It appears as if the exon IV promoter is the major target for corticosterone-mediated transcriptional regulation of BDNF in the hippocampus.
引用
收藏
页码:104 / 114
页数:11
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