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Reelin 和 stk25 在神经元极化和树突高尔基体分布中具有相反的作用。

Reelin and stk25 have opposing roles in neuronal polarization and dendritic Golgi deployment.

机构信息

Department of Neuroscience and Physiology, SUNY Upstate Medical University, Syracuse, NY 13210, USA.

出版信息

Cell. 2010 Nov 24;143(5):826-36. doi: 10.1016/j.cell.2010.10.029.

Abstract

The Reelin ligand regulates a Dab1-dependent signaling pathway required for brain lamination and normal dendritogenesis, but the specific mechanisms underlying these actions remain unclear. We find that Stk25, a modifier of Reelin-Dab1 signaling, regulates Golgi morphology and neuronal polarization as part of an LKB1-Stk25-Golgi matrix protein 130 (GM130) signaling pathway. Overexpression of Stk25 induces Golgi condensation and multiple axons, both of which are rescued by Reelin treatment. Reelin stimulation of cultured neurons induces the extension of the Golgi into dendrites, which is suppressed by Stk25 overexpression. In vivo, Reelin and Dab1 are required for the normal extension of the Golgi apparatus into the apical dendrites of hippocampal and neocortical pyramidal neurons. This demonstrates that the balance between Reelin-Dab1 signaling and LKB1-Stk25-GM130 regulates Golgi dispersion, axon specification, and dendrite growth and provides insights into the importance of the Golgi apparatus for cell polarization.

摘要

Reelin 配体调节 Dab1 依赖性信号通路,该通路对于脑分层和正常树突发生是必需的,但这些作用的具体机制仍不清楚。我们发现,Stk25 是 Reelin-Dab1 信号的调节剂,它作为 LKB1-Stk25-Golgi 基质蛋白 130 (GM130) 信号通路的一部分,调节着高尔基体形态和神经元极化。Stk25 的过表达诱导高尔基体浓缩和多个轴突,这两者都可以通过 Reelin 处理得到挽救。Reelin 对培养神经元的刺激诱导高尔基体延伸到树突中,而过表达 Stk25 会抑制这种延伸。在体内,Reelin 和 Dab1 对于高尔基体在海马和新皮层锥体神经元的树突中正常延伸是必需的。这表明 Reelin-Dab1 信号和 LKB1-Stk25-GM130 之间的平衡调节着高尔基体的分散、轴突的特化以及树突的生长,并为高尔基体对于细胞极化的重要性提供了新的见解。

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