Chiaruttini C, Sonego M, Baj G, Simonato M, Tongiorgi E
BRAIN Centre for Neuroscience, Department of Biology, University of Trieste, 34127 Trieste, Italy.
Mol Cell Neurosci. 2008 Jan;37(1):11-9. doi: 10.1016/j.mcn.2007.08.011. Epub 2007 Aug 23.
Brain-derived neurotrophic factor (BDNF) may exert contrasting effects depending on its different subcellular sites of action (soma, dendrites, axons). These contrasting effects may explain contradictory findings, for example that BDNF may favour or oppose epileptogenesis. We determined the distribution of five BDNF splice variants in the soma and dendrites of rat hippocampal principal neurons, after application of stimuli that prompt BDNF mRNA accumulation in dendrites (epileptogenic seizures). Under basal conditions, no BDNF mRNA splice variant was detectable in dendrites, while specific splice variants were found in dendrites in response to epileptogenic seizures. Three hours after pilocarpine administration, exon VI and exon II splice variants were found in dendrites, while exons I and IV transcripts displayed a strictly somatic localization. Three hours after kainate administration, only exon VI was found in dendrites. These data suggest that the regulated expression of different splice variants may provide a spatial code to ensure the delivery of BDNF to precise destinations in the cell soma or along the dendrites.
脑源性神经营养因子(BDNF)可能因其不同的亚细胞作用位点(胞体、树突、轴突)而产生相反的效应。这些相反的效应可能解释了一些相互矛盾的研究结果,例如BDNF可能促进或抑制癫痫发生。在应用促使BDNF mRNA在树突中积累的刺激(致痫性发作)后,我们测定了大鼠海马体主要神经元胞体和树突中五种BDNF剪接变体的分布。在基础条件下,树突中未检测到BDNF mRNA剪接变体,而在致痫性发作后,树突中发现了特定的剪接变体。毛果芸香碱给药三小时后,树突中发现了外显子VI和外显子II剪接变体,而外显子I和IV转录本则严格定位于胞体。给予 kainate 三小时后,树突中仅发现外显子VI。这些数据表明,不同剪接变体的调控表达可能提供一种空间编码,以确保BDNF被递送至细胞胞体或沿树突的精确靶点。