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神经营养因子可诱导培养的海马神经元之间形成功能性兴奋性和抑制性突触。

Neurotrophins induce formation of functional excitatory and inhibitory synapses between cultured hippocampal neurons.

作者信息

Vicario-Abejón C, Collin C, McKay R D, Segal M

机构信息

Laboratory of Molecular Biology, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland 20892-4092, USA.

出版信息

J Neurosci. 1998 Sep 15;18(18):7256-71. doi: 10.1523/JNEUROSCI.18-18-07256.1998.

Abstract

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.

摘要

利用细胞培养来分析脑源性神经营养因子(BDNF)和神经营养因子-3(NT-3)在突触传递发育中的作用。从胚胎第18天(E18)大鼠海马体获取的神经元并培养2周后,表现出广泛的自发突触活动。相比之下,从E16海马体获取的神经元表达的自发或诱发突触活动水平非常低。神经营养因子处理使E16培养物中功能性突触连接的数量增加了7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。这些效应与血清或用于培养的神经胶质床的年龄无关。它们并未伴随着突触小泡相关蛋白或谷氨酸受体的显著变化。用神经营养因子处理培养物3天足以建立功能性突触的最大水平。在此期间,神经营养因子不影响兴奋性神经元的活力或形态,尽管它们确实使GABA能神经元的树突数量和长度增加。值得注意的是,只有BDNF导致GABA能神经元的轴突分支数量和轴突总长度增加。这些结果支持神经营养因子在发育中的海马体兴奋性和抑制性突触形成中具有独特且不同的作用。

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