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DEAD-box蛋白在少突胶质细胞发育、分化和稳态中的多种功能。

Diverse functions of DEAD-box proteins in oligodendrocyte development, differentiation, and homeostasis.

作者信息

Bizen Norihisa, Takebayashi Hirohide

机构信息

Division of Neurobiology and Anatomy, Graduate School of Medical and Dental Sciences, Niigata University, Niigata, Japan.

Center for Anatomical Studies, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

出版信息

J Neurochem. 2025 Jan;169(1):e16238. doi: 10.1111/jnc.16238. Epub 2024 Oct 7.

Abstract

Oligodendrocytes, a type of glial cell in the central nervous system, have a critical role in the formation of myelin around axons, facilitating saltatory conduction, and maintaining the integrity of nerve axons. The dysregulation of oligodendrocyte differentiation and homeostasis have been implicated in a wide range of neurological diseases, including dysmyelinating disorders (e.g., Pelizaeus-Merzbacher disease), demyelinating diseases (e.g., multiple sclerosis), Alzheimer's disease, and psychiatric disorders. Therefore, unraveling the mechanisms of oligodendrocyte development, differentiation, and homeostasis is essential for understanding the pathogenesis of these diseases and the development of therapeutic interventions. Numerous studies have identified and analyzed the functions of transcription factors, RNA metabolic factors, translation control factors, and intracellular and extracellular signals involved in the series of processes from oligodendrocyte fate determination to terminal differentiation. DEAD-box proteins, multifunctional RNA helicases that regulate various intracellular processes, including transcription, RNA processing, and translation, are increasingly recognized for their diverse roles in various aspects of oligodendrocyte development, differentiation, and maintenance of homeostasis. This review introduces the latest insights into the regulatory networks of oligodendrocyte biology mediated by DEAD-box proteins.

摘要

少突胶质细胞是中枢神经系统中的一种神经胶质细胞,在轴突周围髓鞘的形成、促进跳跃式传导以及维持神经轴突的完整性方面发挥着关键作用。少突胶质细胞分化和稳态的失调与多种神经系统疾病有关,包括脱髓鞘疾病(如佩利措伊斯-梅茨巴赫病)、髓鞘脱失疾病(如多发性硬化症)、阿尔茨海默病和精神疾病。因此,阐明少突胶质细胞发育、分化和稳态的机制对于理解这些疾病的发病机制和开发治疗干预措施至关重要。众多研究已经鉴定并分析了从少突胶质细胞命运决定到终末分化这一系列过程中涉及的转录因子、RNA代谢因子、翻译控制因子以及细胞内和细胞外信号的功能。DEAD-box蛋白是一类多功能RNA解旋酶,可调节包括转录、RNA加工和翻译在内的各种细胞内过程,它们在少突胶质细胞发育、分化和稳态维持的各个方面所起的不同作用越来越受到认可。本综述介绍了由DEAD-box蛋白介导的少突胶质细胞生物学调控网络的最新见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85ac/11658190/6f2f328ec8da/JNC-169-0-g001.jpg

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