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MicroRNA132 调节海马神经元的短期突触可塑性,但不调节基础释放概率。

MicroRNA132 modulates short-term synaptic plasticity but not basal release probability in hippocampal neurons.

机构信息

Graduate Program in Neurobiology and Behavior, University of Washington, Seattle, Washington, United States of America.

出版信息

PLoS One. 2010 Dec 29;5(12):e15182. doi: 10.1371/journal.pone.0015182.

Abstract

MicroRNAs play important regulatory roles in a broad range of cellular processes including neuronal morphology and long-term synaptic plasticity. MicroRNA-132 (miR132) is a CREB-regulated miRNA that is induced by neuronal activity and neurotrophins, and plays a role in regulating neuronal morphology and cellular excitability. Little is known about the effects of miR132 expression on synaptic function. Here we show that overexpression of miR132 increases the paired-pulse ratio and decreases synaptic depression in cultured mouse hippocampal neurons without affecting the initial probability of neurotransmitter release, the calcium sensitivity of release, the amplitude of excitatory postsynaptic currents or the size of the readily releasable pool of synaptic vesicles. These findings are the first to demonstrate that microRNAs can regulate short-term plasticity in neurons.

摘要

微小 RNA 在广泛的细胞过程中发挥重要的调节作用,包括神经元形态和长时程突触可塑性。微小 RNA-132 (miR132) 是一种 CREB 调控的微小 RNA,由神经元活动和神经营养因子诱导,在调节神经元形态和细胞兴奋性方面发挥作用。关于 miR132 表达对突触功能的影响知之甚少。在这里,我们发现过表达 miR132 会增加培养的小鼠海马神经元的成对脉冲比,减少突触抑制,而不影响神经递质释放的初始概率、释放的钙敏感性、兴奋性突触后电流的幅度或可释放突触囊泡的易释放池的大小。这些发现首次证明微小 RNA 可以调节神经元的短期可塑性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64f3/3012071/5ed933bf5b53/pone.0015182.g001.jpg

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