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神经退行性疾病中小GTP酶的Rho和Rab家族之间的串扰。

Crosstalk between the Rho and Rab family of small GTPases in neurodegenerative disorders.

作者信息

Nik Akhtar Shayan, Bunner Wyatt P, Brennan Elizabeth, Lu Qun, Szatmari Erzsebet M

机构信息

The Harriet and John Wooten Laboratory for Alzheimer's and Neurodegenerative Diseases Research, Brody School of Medicine, East Carolina University, Greenville, NC, United States.

Laboratory of Neuroscience, Department of Physical Therapy, College of Allied Health Sciences, East Carolina University, Greenville, NC, United States.

出版信息

Front Cell Neurosci. 2023 Jan 27;17:1084769. doi: 10.3389/fncel.2023.1084769. eCollection 2023.

Abstract

Neurodegeneration is associated with defects in cytoskeletal dynamics and dysfunctions of the vesicular trafficking and sorting systems. In the last few decades, studies have demonstrated that the key regulators of cytoskeletal dynamics are proteins from the Rho family GTPases, meanwhile, the central hub for vesicle sorting and transport between target membranes is the Rab family of GTPases. In this regard, the role of Rho and Rab GTPases in the induction and maintenance of distinct functional and morphological neuronal domains (such as dendrites and axons) has been extensively studied. Several members belonging to these two families of proteins have been associated with many neurodegenerative disorders ranging from dementia to motor neuron degeneration. In this analysis, we attempt to present a brief review of the potential crosstalk between the Rab and Rho family members in neurodegenerative pathologies such as Alzheimer's disease (AD), Parkinson's disease (PD), Huntington disease, and amyotrophic lateral sclerosis (ALS).

摘要

神经退行性变与细胞骨架动力学缺陷以及囊泡运输和分选系统功能障碍有关。在过去几十年中,研究表明细胞骨架动力学的关键调节因子是Rho家族GTP酶蛋白,同时,囊泡分选和靶膜间运输的核心枢纽是Rab家族GTP酶。在这方面,Rho和Rab GTP酶在诱导和维持不同功能及形态的神经元区域(如树突和轴突)中的作用已得到广泛研究。这两个蛋白家族的几个成员已与从痴呆到运动神经元变性等许多神经退行性疾病相关联。在本分析中,我们试图简要综述Rab和Rho家族成员在阿尔茨海默病(AD)、帕金森病(PD)、亨廷顿病和肌萎缩侧索硬化症(ALS)等神经退行性病变中的潜在相互作用。

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