与海马体突触长期抑制相关的树突棘收缩。

Shrinkage of dendritic spines associated with long-term depression of hippocampal synapses.

作者信息

Zhou Qiang, Homma Koichi J, Poo Mu-ming

机构信息

Division of Neurobiology, Department of Molecular and Cell Biology, Helen Will Neuroscience Institute, University of California, Berkeley, Berkeley, CA 94720, USA.

出版信息

Neuron. 2004 Dec 2;44(5):749-57. doi: 10.1016/j.neuron.2004.11.011.

Abstract

Activity-induced modification of neuronal connections is essential for the development of the nervous system and may also underlie learning and memory functions of mature brain. Previous studies have shown an increase in dendritic spine density and/or enlargement of spines after the induction of long-term potentiation (LTP). Using two-photon time-lapse imaging of dendritic spines in acute hippocampal slices from neonatal rats, we found that the induction of long-term depression (LTD) by low-frequency stimulation is accompanied by a marked shrinkage of spines, which can be reversed by subsequent high-frequency stimulation that induces LTP. The spine shrinkage requires activation of NMDA receptors and calcineurin, similar to that for LTD. However, spine shrinkage is mediated by cofilin, but not by protein phosphatase 1 (PP1), which is essential for LTD, suggesting that different downstream pathways are involved in spine shrinkage and LTD. This activity-induced spine shrinkage may contribute to activity-dependent elimination of synaptic connections.

摘要

活动诱导的神经元连接修饰对于神经系统的发育至关重要,也可能是成熟大脑学习和记忆功能的基础。先前的研究表明,在诱导长时程增强(LTP)后,树突棘密度增加和/或棘增大。利用新生大鼠急性海马切片中树突棘的双光子延时成像,我们发现低频刺激诱导长时程抑制(LTD)伴随着棘的显著收缩,随后诱导LTP的高频刺激可使其逆转。棘收缩需要NMDA受体和钙调神经磷酸酶的激活,这与LTD相似。然而,棘收缩是由丝切蛋白介导的,而不是由LTD所必需的蛋白磷酸酶1(PP1)介导的,这表明不同的下游途径参与了棘收缩和LTD。这种活动诱导的棘收缩可能有助于依赖活动的突触连接消除。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索