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脑源性神经营养因子(BDNF)调节 Rab11 介导的循环内体动力学,诱导树突分支。

BDNF regulates Rab11-mediated recycling endosome dynamics to induce dendritic branching.

机构信息

Neuronal Cell Biology and Regeneration Laboratory, Millennium Nucleus of Regenerative Biology, Center of Aging and Regeneration, Departamento de Fisiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago CP 8331010, Chile.

出版信息

J Neurosci. 2013 Apr 3;33(14):6112-22. doi: 10.1523/JNEUROSCI.4630-12.2013.

Abstract

Dendritic arborization of neurons is regulated by brain-derived neurotrophic factor (BDNF) together with its receptor, TrkB. Endocytosis is required for dendritic branching and regulates TrkB signaling, but how postendocytic trafficking determines the neuronal response to BDNF is not well understood. The monomeric GTPase Rab11 regulates the dynamics of recycling endosomes and local delivery of receptors to specific dendritic compartments. We investigated whether Rab11-dependent trafficking of TrkB in dendrites regulates BDNF-induced dendritic branching in rat hippocampal neurons. We report that TrkB in dendrites is a cargo for Rab11 endosomes and that both Rab11 and its effector, MyoVb, are required for BDNF/TrkB-induced dendritic branching. In addition, BDNF induces the accumulation of Rab11-positive endosomes and GTP-bound Rab11 in dendrites and the expression of a constitutively active mutant of Rab11 is sufficient to increase dendritic branching by increasing TrkB localization in dendrites and enhancing sensitization to endogenous BDNF. We propose that Rab11-dependent dendritic recycling provides a mechanism to retain TrkB in dendrites and to increase local signaling to regulate arborization.

摘要

神经元树突分支由脑源性神经营养因子(BDNF)与其受体 TrkB 共同调控。内吞作用是树突分支所必需的,并且调节 TrkB 信号转导,但内吞作用后转运如何决定神经元对 BDNF 的反应尚不清楚。单体 GTPase Rab11 调节循环内体的动态变化和受体向特定树突隔室的局部输送。我们研究了树突中 Rab11 依赖性 TrkB 转运是否调节大鼠海马神经元中 BDNF 诱导的树突分支。我们报告说,树突中的 TrkB 是 Rab11 内体的货物,并且 Rab11 和其效应物 MyoVb 都需要 BDNF/TrkB 诱导的树突分支。此外,BDNF 诱导 Rab11 阳性内体和 GTP 结合的 Rab11 在树突中的积累,并且组成型激活的 Rab11 突变体的表达足以通过增加树突中 TrkB 的定位和增强对内源性 BDNF 的敏感性来增加树突分支。我们提出 Rab11 依赖性树突再循环提供了一种机制来保留树突中的 TrkB 并增加局部信号转导以调节分支。

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