Meng Hongdi, Gao Rui, Dai Qun, Qiao Xiaoxi
Department of Ophthalmology, Pharmacology and Neuroscience, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Neuropharmacology. 2007 Jul;53(1):81-91. doi: 10.1016/j.neuropharm.2007.04.012. Epub 2007 May 1.
Activity-dependent regulation of BDNF expression plays important roles in synaptic plasticity and neuronal function. We have investigated glutamate receptor-mediated regulation of BDNF expression in the cerebellum of wild-type and stargazer (stg) mice. Both in vivo and in vitro studies revealed that BDNF response kinetics in the cerebellum were much delayed with reversed sensitivity to NMDA versus non-NMDA agonist exposures significantly different from those in the cortex and hippocampus of wild-type mice. In stg mice, the severely impaired BDNF expression was restricted to the cerebellum while responses in the forebrain were intact. A selective failure of BDNF mRNA response to AMPA stimulation, but not NMDA, was evident in cultured stg cerebellar granule cells. These results demonstrate that BDNF expression is differentially regulated with region-specific kinetics. It indicates that the BDNF expression defect in the stg cerebellum is attributable to the AMPA receptor defect caused by the stargazin mutation.
脑源性神经营养因子(BDNF)表达的活动依赖性调节在突触可塑性和神经元功能中起重要作用。我们研究了野生型和凝视(stg)小鼠小脑中谷氨酸受体介导的BDNF表达调节。体内和体外研究均显示,与野生型小鼠的皮层和海马相比,小脑中BDNF的反应动力学明显延迟,对NMDA与非NMDA激动剂暴露的敏感性相反。在stg小鼠中,严重受损的BDNF表达仅限于小脑,而前脑的反应则完好无损。在培养的stg小脑颗粒细胞中,明显存在BDNF mRNA对AMPA刺激而非NMDA刺激的选择性反应失败。这些结果表明,BDNF表达受区域特异性动力学的差异调节。这表明stg小脑BDNF表达缺陷归因于stargazin突变引起的AMPA受体缺陷。