首页> 美国卫生研究院文献>The Journal of Neuroscience >Increased Expression of Brain-Derived Neurotrophic Factor Induces Formation of Basal Dendrites and Axonal Branching in Dentate Granule Cells in Hippocampal Explant Cultures
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Increased Expression of Brain-Derived Neurotrophic Factor Induces Formation of Basal Dendrites and Axonal Branching in Dentate Granule Cells in Hippocampal Explant Cultures

机译:脑源性神经营养因子表达的增加导致海马外植体培养物中齿状颗粒细胞基底树突的形成和轴突分支。

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摘要

During limbic epileptogenesis in vivo the dentate granule cells (DGCs) exhibit increased expression of brain-derived neurotrophic factor (BDNF), followed by striking morphologic plasticities, namely the formation of basal dendrites and the sprouting of mossy fibers. We hypothesized that increased expression of BDNF intrinsic to DGCs is sufficient to induce these plasticities. To test this hypothesis, we transfected DGCs in rat hippocampal slice cultures with BDNF or nerve growth factor (NGF) via particle-mediated gene transfer, and we visualized the neuronal processes with cotransfected green fluorescent protein. Transfection with BDNF produced significant increases in axonal branch and basal dendrite number relative to NGF or empty vector controls. Structural changes were prevented by the tyrosine kinase inhibitor K252a. Thus increased expression of BDNF within DGCs is sufficient to induce these morphological plasticities, which may represent one mechanism by which BDNF promotes limbic epileptogenesis.
机译:在体内边缘性癫痫发生过程中,齿状颗粒细胞(DGC)表现出脑源性神经营养因子(BDNF)的表达增加,随后出现形态可塑性,即基底树突的形成和苔藓纤维的萌芽。我们假设DGC固有的BDNF表达的增加足以诱导这些可塑性。为了验证这一假设,我们通过颗粒介导的基因转移,用BDNF或神经生长因子(NGF)转染了大鼠海马切片培养物中的DGC,并用共转染的绿色荧光蛋白可视化了神经元过程。相对于NGF或空载体对照,用BDNF转染可显着增加轴突分支和基底树突的数量。酪氨酸激酶抑制剂K252a可防止结构改变。因此,在DGC中BDNF表达的增加足以诱导这些形态可塑性,这可能代表BDNF促进边缘性癫痫发生的一种机制。

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