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RCAN1 调节双向突触可塑性。

RCAN1 Regulates Bidirectional Synaptic Plasticity.

机构信息

Département Neurosciences, Groupe de Recherche sur le Système Nerveux Central, Université de Montréal, Montréal, QC H3T 1J4, Canada.

Département Neurosciences, Groupe de Recherche sur le Système Nerveux Central, Université de Montréal, Montréal, QC H3T 1J4, Canada; Centre de Recherche, Centre Hospitalier Universitaire Sainte-Justine, Montréal, QC H3T 1C5, Canada.

出版信息

Curr Biol. 2020 Apr 6;30(7):1167-1176.e2. doi: 10.1016/j.cub.2020.01.041. Epub 2020 Feb 20.

Abstract

Synaptic plasticity, with its two most studied forms, long-term potentiation (LTP) and long-term depression (LTD), is the cellular mechanism underlying learning and memory. Although it has been known for two decades that bidirectional synaptic plasticity necessitates a corresponding bidirectional regulation of calcineurin activity, the underlying molecular mechanism remains elusive. Using organotypic hippocampal slice cultures, we show here that phosphorylation of the endogenous regulator-of-calcineurin (RCAN1) by GSK3β underlies calcineurin activation and is a necessary event for LTD induction, while phosphorylation of RCAN1 at a PKA site blocks calcineurin activity, thereby allowing LTP induction. Our results provide a new mechanism for the regulation of calcineurin in bidirectional synaptic plasticity and establish RCAN1 as a "switch" for bidirectional synaptic plasticity.

摘要

突触可塑性及其两种最具研究价值的形式

长时程增强(LTP)和长时程抑制(LTD),是学习和记忆的细胞机制。尽管人们已经知道了二十年,双向突触可塑性需要钙调神经磷酸酶活性的相应双向调节,但潜在的分子机制仍然难以捉摸。使用器官型海马切片培养物,我们在这里表明,GSK3β 对内源性钙调神经磷酸酶调节剂(RCAN1)的磷酸化是钙调神经磷酸酶激活的基础,也是 LTD 诱导所必需的事件,而 RCAN1 在 PKA 位点的磷酸化则阻止钙调神经磷酸酶的活性,从而允许 LTP 的诱导。我们的结果为钙调神经磷酸酶在双向突触可塑性中的调节提供了一个新的机制,并确立了 RCAN1 作为双向突触可塑性的“开关”。

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