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通过Rho/ Rho激酶信号通路实现皮质纹状体神经元的存活。

Survival of corticostriatal neurons by Rho/Rho-kinase signaling pathway.

作者信息

Kobayashi Kenta, Sano Hiromi, Kato Shigeki, Kuroda Keisuke, Nakamuta Shinichi, Isa Tadashi, Nambu Atsushi, Kaibuchi Kozo, Kobayashi Kazuto

机构信息

Section of Viral Vector Development, National Institute for Physiological Sciences, Okazaki 444-8585, Japan; SOKENDAI (The Graduate University for Advanced Studies), Hayama 240-0193, Japan.

SOKENDAI (The Graduate University for Advanced Studies), Hayama 240-0193, Japan; Division of System Neurophysiology, National Institute for Physiological Sciences, Okazaki 444-8585, Japan.

出版信息

Neurosci Lett. 2016 Sep 6;630:45-52. doi: 10.1016/j.neulet.2016.07.020. Epub 2016 Jul 15.

Abstract

Developing cortical neurons undergo a number of sequential developmental events including neuronal survival/apoptosis, and the molecular mechanism underlying each characteristic process has been studied in detail. However, the survival pathway of cortical neurons at mature stages remains largely uninvestigated. We herein focused on mature corticostriatal neurons because of their important roles in various higher brain functions and the spectrum of neurological and neuropsychiatric disorders. The small GTPase Rho is known to control diverse and essential cellular functions through some effector molecules, including Rho-kinase, during neural development. In the present study, we investigated the role of Rho signaling through Rho-kinase in the survival of corticostriatal neurons. We performed the conditional expression of Clostridium botulinum C3 ADP-ribosyltransferase (C3 transferase) or dominant-negative form for Rho-kinase (Rho-K DN), a well-known inhibitor of Rho or Rho-kinase, respectively, in corticostriatal neurons using a dual viral vector approach combining a neuron-specific retrograde gene transfer lentiviral vector and an adeno-associated virus vector. C3 transferase markedly decreased the number of corticostriatal neurons, which was attributed to caspase-3-dependent enhanced apoptosis. In addition, Rho-K DN produced phenotypic defects similar to those caused by C3 transferase. These results indicate that the Rho/Rho-kinase signaling pathway plays a crucial role in the survival of corticostriatal neurons.

摘要

正在发育的皮质神经元会经历一系列连续的发育事件,包括神经元存活/凋亡,并且每个特征性过程背后的分子机制都已得到详细研究。然而,成熟阶段皮质神经元的存活途径在很大程度上仍未被研究。由于其在各种高级脑功能以及一系列神经和神经精神疾病中发挥的重要作用,我们在此聚焦于成熟的皮质纹状体神经元。已知小GTP酶Rho在神经发育过程中通过一些效应分子(包括Rho激酶)来控制多种重要的细胞功能。在本研究中,我们研究了通过Rho激酶的Rho信号在皮质纹状体神经元存活中的作用。我们使用一种结合神经元特异性逆行基因转移慢病毒载体和腺相关病毒载体的双病毒载体方法,在皮质纹状体神经元中分别进行了肉毒杆菌C3 ADP核糖基转移酶(C3转移酶)或Rho激酶显性负性形式(Rho-K DN)(分别是Rho或Rho激酶的著名抑制剂)的条件性表达。C3转移酶显著减少了皮质纹状体神经元的数量,这归因于caspase-3依赖性增强的细胞凋亡。此外,Rho-K DN产生了与C3转移酶引起的类似的表型缺陷。这些结果表明,Rho/Rho激酶信号通路在皮质纹状体神经元的存活中起关键作用。

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