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神经连接蛋白控制成熟的、性别二态性神经元的可塑性。

Neurexin controls plasticity of a mature, sexually dimorphic neuron.

机构信息

1Department of Biological Sciences, Howard Hughes Medical Institute, Columbia University, New York, New York, USA.

出版信息

Nature. 2018 Jan 10;553(7687):165-170. doi: 10.1038/nature25192.

Abstract

During development and adulthood, brain plasticity is evident at several levels, from synaptic structure and function to the outgrowth of dendrites and axons. Whether and how sex impinges on neuronal plasticity is poorly understood. Here we show that the sex-shared GABA (γ-aminobutyric acid)-releasing DVB neuron in Caenorhabditis elegans displays experience-dependent and sexually dimorphic morphological plasticity, characterized by the stochastic and dynamic addition of multiple neurites in adult males. These added neurites enable synaptic rewiring of the DVB neuron and instruct a functional switch of the neuron that directly modifies a step of male mating behaviour. Both DVB neuron function and male mating behaviour can be altered by experience and by manipulation of postsynaptic activity. The outgrowth of DVB neurites is promoted by presynaptic neurexin and antagonized by postsynaptic neuroligin, revealing a non-conventional activity and mode of interaction of these conserved, human-disease-relevant factors.

摘要

在发育和成年过程中,大脑可塑性在多个层面上表现明显,从突触结构和功能到树突和轴突的生长。性如何影响神经元可塑性尚不清楚。在这里,我们展示了秀丽隐杆线虫中性别共享的 GABA(γ-氨基丁酸)释放 DVB 神经元表现出经验依赖性和性别二态性的形态可塑性,其特征是成年雄性中多个神经元随机和动态地添加。这些添加的神经元使 DVB 神经元的突触重新布线,并指导神经元的功能转换,从而直接改变雄性交配行为的一个步骤。DVB 神经元功能和雄性交配行为都可以通过经验和对突触后活动的操纵来改变。DVB 神经元的轴突生长由突触前神经连接蛋白促进,由突触后神经黏附蛋白拮抗,揭示了这些保守的、与人类疾病相关的因素的非传统活性和相互作用模式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/715f/5968453/bd0f33020ff4/nihms925168f5.jpg

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