髓鞘
斑马鱼
多发性硬化
中枢神经系统
肿胀 的
化学
细胞生物学
髓鞘碱性蛋白
神经科学
髓鞘
少突胶质细胞
生物物理学
生物
人脑
白质
解剖
作者
Donia Arafa,Julia van de Korput,Philipp N. Braaker,Kieran Higgins,Niels R. C. Meijns,Katy L. H. Marshall-Phelps,Julia Meng,Daniel Soong,Eleonora Scalia,Kyle Lathem,Marcus Keatinge,Claire Richmond,Anna Klingseisen,Marja Main,Sarah A. Neely,David W. Hampton,Greg J. Duncan,Geert J. Schenk,Marie Louise Groot,Siddharthan Chandran
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2026-02-12
卷期号:391 (6786): eadr4661-eadr4661
被引量:2
标识
DOI:10.1126/science.adr4661
摘要
Myelin damage is a hallmark of several neurological disorders, but how it occurs remains to be fully understood. In this study, we found that early damage in zebrafish and rodent demyelination models is characterized by myelin swelling. We show, through live imaging, that myelin swelling does not always lead to myelin loss and that swellings can sometimes resolve, allowing sheaths to remodel. Increased neuronal activity during early demyelination exacerbates myelin damage, whereas reducing neuronal activity mitigates myelin swelling in both zebrafish and mice. In human multiple sclerosis tissue, myelin swelling is also dynamic and is prominent around active lesions. Our data indicate that myelin swelling is a conserved feature of demyelination and that damage to myelin sheaths can resolve, opening opportunities for targeting human disease.
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