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中枢神经系统脱髓鞘和髓鞘再生过程中脂质代谢的改变是推动多发性硬化症进展的关键因素。

Altered Lipid Metabolism in CNS Demyelination and Remyelination Are Key Elements Driving Progressive MS.

作者信息

Matejuk Agata, Matejuk Szymon, Offner Halina, Vandenbark Arthur A

机构信息

Department of Immunology, Collegium Medicum, University of Zielona Góra, 65-417 Zielona Góra, Poland.

Department of Internal Medicine, University of South Alabama, 2451 University Hospital Dr., Mobile, AL 36617, USA.

出版信息

Int J Mol Sci. 2025 Aug 27;26(17):8314. doi: 10.3390/ijms26178314.

Abstract

Lipids, together with water and proteins, constitute the essential structure of cell membranes, and in the CNS, critically contribute to the production, function, and maintenance of the myelin sheath. Myelin produced by oligodendrocytes (OLs) acts as an electric insulator and assures proper conduction of information. Three major fractions of myelin lipids are cholesterol, phospholipids, and glycolipids. These lipids not only sculpt the myelin landscape as a structural support for proteins, but they also play a crucial role in molecular interactions underlying processes of protein trafficking and signal transductions. The high lipid content of myelin makes it susceptible to lipid metabolism disorders. Disorders in systemic and local lipid metabolism may lead to loss of myelin integrity and stability, and potentially to CNS demyelination seen in neurodegenerative diseases, notably progressive multiple sclerosis, for which there are few effective therapies. Precise interactions among disorders in lipid metabolism, function of oligodendrocytes, and demyelination/remyelination events, including de novo myelin formation and myelin remodeling processes, may lay the foundation for novel therapeutics for progressive MS and other demyelinating CNS conditions.

摘要

脂质与水和蛋白质一起构成细胞膜的基本结构,在中枢神经系统中,对髓鞘的产生、功能和维持起着关键作用。少突胶质细胞(OLs)产生的髓鞘起到电绝缘体的作用,确保信息的正常传导。髓鞘脂质的三个主要部分是胆固醇、磷脂和糖脂。这些脂质不仅塑造了髓鞘结构,为蛋白质提供结构支持,还在蛋白质运输和信号转导过程的分子相互作用中发挥关键作用。髓鞘的高脂质含量使其易受脂质代谢紊乱的影响。全身和局部脂质代谢紊乱可能导致髓鞘完整性和稳定性丧失,并可能导致神经退行性疾病中出现的中枢神经系统脱髓鞘,尤其是进行性多发性硬化症,目前针对该病的有效治疗方法很少。脂质代谢紊乱、少突胶质细胞功能以及脱髓鞘/再髓鞘化事件(包括新生髓鞘形成和髓鞘重塑过程)之间的精确相互作用,可能为进行性多发性硬化症和其他中枢神经系统脱髓鞘疾病的新型治疗方法奠定基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97f1/12427691/c18bacbccb3b/ijms-26-08314-g001.jpg

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