Department of Anesthesiology, Kitasato University School of Medicine, Sagamihara 252-0374, Kanagawa, Japan.
Department of Anatomy, Kitasato University School of Medicine, Sagamihara 252-0374, Kanagawa, Japan.
Int J Mol Sci. 2022 May 3;23(9):5087. doi: 10.3390/ijms23095087.
The cytohesin proteins, consisting of four closely related members (cytohesins-1, -2, -3, and -4), are a subfamily of the Sec7 domain-containing guanine nucleotide exchange factors for ADP ribosylation factors (Arfs), which are critical regulators of membrane trafficking and actin cytoskeleton remodeling. Recent advances in molecular biological techniques and the development of a specific pharmacological inhibitor for cytohesins, SecinH3, have revealed the functional involvement of the cytohesin-Arf pathway in diverse neuronal functions from the formation of axons and dendrites, axonal pathfinding, and synaptic vesicle recycling, to pathophysiological processes including chronic pain and neurotoxicity induced by proteins related to neurodegenerative disorders, such as amyotrophic lateral sclerosis and Alzheimer's disease. Here, we review the physiological and pathological roles of the cytohesin-Arf pathway in neurons and discuss the future directions of this research field.
细胞松弛素蛋白由四个密切相关的成员(细胞松弛素-1、-2、-3 和 -4)组成,是 ADP 核糖基化因子(Arfs)的 Sec7 结构域包含的鸟嘌呤核苷酸交换因子的一个亚家族,Arfs 是膜运输和肌动蛋白细胞骨架重塑的关键调节剂。分子生物学技术的最新进展和细胞松弛素蛋白 SecinH3 的特异性药理学抑制剂的开发,揭示了细胞松弛素-Arf 途径在从轴突和树突形成、轴突寻径和突触小泡再循环到包括慢性疼痛和与神经退行性疾病相关的蛋白质(如肌萎缩侧索硬化症和阿尔茨海默病)引起的神经毒性等多种神经元功能中的功能相关性。在这里,我们综述了细胞松弛素-Arf 途径在神经元中的生理和病理作用,并讨论了该研究领域的未来方向。