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突触前蛋白突触融合蛋白 1 调节培养海马神经元中活性诱导的突触结构重塑。

Presynaptic protein synaptotagmin1 regulates the activity-induced remodeling of synaptic structures in cultured hippocampal neurons.

机构信息

Department of Anatomy, School of Medicine, Faculty of Medicine, Toho University, Tokyo, Japan.

出版信息

J Neurosci Res. 2013 Jul;91(7):882-9. doi: 10.1002/jnr.23215. Epub 2013 Apr 22.

Abstract

Activity-dependent reorganizations of central neuronal synapses are thought to play important roles in learning and memory. Although the precise mechanisms of how neuronal activities modify synaptic connections in neurons remain to be clarified, the activity-induced neuronal presynaptic proteins such as synaptotagmin1 may contribute to the onset of synaptic remodeling. To understand better the physiological roles of synaptotagmin1, we first examined the prolonged effects of neuronal stimulation capable of inducing synaptotagmin1 on the distribution of a postsynaptic proteins (PSD) protein Homer1c by immunostaining. Previously we found that glutamate stimulation induced other postsynaptic proteins, such as postsynaptic density-95 (PSD95), a biphasic change with an initially diffuse distribution after 30 min to 1 hr, followed by reassembly to more than the original level after 4-8 hr, suggesting that glutamate stimulation induces a global biphasic alteration in synaptic structures. To dissect further the functions of synaptotagmin1 in the activity-induced synaptic remodeling, short hairpin RNA (shRNA) vectors that specifically block the expression of endogenous synaptotagmin1 were constructed. When the shRNA of synaptotagmin1 was introduced to the neurons, the activity-induced changes were almost completely suppressed. We found that synaptotagmin1 contributes to the postsynaptic remodeling in a retrograde manner. Our data indicate that synaptotagmin1 regulates the activity-induced biphasic changes of post- and presynaptic sites.

摘要

活动依赖性的中枢神经元突触重组被认为在学习和记忆中发挥重要作用。尽管神经元活动如何改变神经元中突触连接的确切机制仍有待阐明,但神经元活动诱导的突触前蛋白,如突触融合蛋白 1(synaptotagmin1),可能有助于突触重塑的开始。为了更好地理解突触融合蛋白 1 的生理作用,我们首先通过免疫染色检查了能够诱导突触融合蛋白 1 的神经元刺激的延长作用对突触后蛋白(PSD)蛋白 Homer1c 的分布的影响。之前我们发现谷氨酸刺激诱导了其他突触后蛋白,如突触后密度蛋白 95(PSD95),在 30 分钟到 1 小时后出现初始弥散分布的双相变化,然后在 4-8 小时后重新组装到超过原始水平,表明谷氨酸刺激诱导了突触结构的全局双相改变。为了进一步剖析突触融合蛋白 1 在活动诱导的突触重塑中的功能,我们构建了特异性阻断内源性突触融合蛋白 1 表达的短发夹 RNA(shRNA)载体。当将突触融合蛋白 1 的 shRNA 引入神经元时,活动诱导的变化几乎完全被抑制。我们发现突触融合蛋白 1 以逆行方式参与突触后重塑。我们的数据表明,突触融合蛋白 1 调节活动诱导的突触前和突触后位点的双相变化。

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