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Neurotrophins Induce Formation of Functional Excitatory and Inhibitory Synapses between Cultured Hippocampal Neurons

机译:Neurotrophins诱导培养的海马神经元之间的功能性兴奋和抑制性突触的形成。

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摘要

Cell cultures were used to analyze the role of brain-derived neurotrophic factor (BDNF) and neurotrophin-3 (NT-3) in the development of synaptic transmission. Neurons obtained from embryonic day 18 (E18) rat hippocampus and cultured for 2 weeks exhibited extensive spontaneous synaptic activity. By comparison, neurons obtained from E16 hippocampus expressed very low levels of spontaneous or evoked synaptic activity. Neurotrophin treatment produced a sevenfold increase in the number of functional synaptic connections in the E16 cultures. BDNF induced formation of both excitatory and inhibitory synapses, whereas NT-3 induced formation of only excitatory synapses. These effects were independent of serum or the age of the glia bed used for the culture. They were not accompanied by significant changes in synaptic-vesicle-associated proteins or glutamate receptors. Treatment of the cultures with the neurotrophins for 3 d was sufficient to establish the maximal level of functional synapses. During this period, neurotrophins did not affect the viability or the morphology of the excitatory neurons, although they did produce an increase in the number and length of dendrites of the GABAergic neurons. Remarkably, only BDNF caused an increase in the number of axonal branches and in the total length of the axons of the GABAergic neurons. These results support a unique and differential role for neurotrophins in the formation of excitatory and inhibitory synapses in the developing hippocampus.
机译:细胞培养用于分析脑源性神经营养因子(BDNF)和神经营养蛋白3(NT-3)在突触传递中的作用。从胚胎第18天(E18)大鼠海马中获取并培养2周的神经元表现出广泛的自发突触活性。相比之下,从E16海马获得的神经元表达的自发或诱发突触活性水平很低。 Neurotrophin治疗在E16培养物中的功能性突触连接数量增加了七倍。 BDNF诱导兴奋性和抑制性突触的形成,而NT-3仅诱导兴奋性突触的形成。这些影响与血清或用于培养的神经胶质床的年龄无关。它们并没有伴随突触小泡相关蛋白或谷氨酸受体的显着变化。用神经营养蛋白处理培养物3天足以建立最大水平的功能性突触。在此期间,尽管神经营养蛋白确实会增加GABA能神经元树突的数量和长度,但它们不会影响兴奋性神经元的活力或形态。值得注意的是,仅BDNF引起了GABA能神经元的轴突分支数量和轴突总长度的增加。这些结果支持神经营养蛋白在发育中的海马体中兴奋性和抑制性突触的形成中的独特和差异作用。

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