瓜氨酸化
少突胶质细胞
髓鞘少突胶质细胞糖蛋白
生物
神经科学
髓鞘
神经退行性变
细胞生物学
遗传学
瓜氨酸
医学
内科学
精氨酸
中枢神经系统
氨基酸
疾病
作者
Ana Mendanha Falcão,Mandy Meijer,Antonella Scaglione,Puneet Rinwa,Eneritz Agirre,Jialiang Liang,Sara Charlotte Buch-Larsen,Abeer Heskol,Rebecca Frawley,Michael Klingener,Manuel Varas‐Godoy,Alexandre A. S. F. Raposo,Patrik Ernfors,Diogo S. Castro,Michael Lund Nielsen,Patrizia Casaccia,Gonçalo Castelo‐Branco
出处
期刊:Cell Reports
[Cell Press]
日期:2019-04-01
卷期号:27 (4): 1090-1102.e10
被引量:97
标识
DOI:10.1016/j.celrep.2019.03.108
摘要
Citrullination, the deimination of peptidylarginine residues into peptidylcitrulline, has been implicated in the etiology of several diseases. In multiple sclerosis, citrullination is thought to be a major driver of pathology through hypercitrullination and destabilization of myelin. As such, inhibition of citrullination has been suggested as a therapeutic strategy for MS. Here, in contrast, we show that citrullination by peptidylarginine deiminase 2 (PAD2) contributes to normal oligodendrocyte differentiation, myelination, and motor function. We identify several targets for PAD2, including myelin and chromatin-related proteins, implicating PAD2 in epigenomic regulation. Accordingly, we observe that PAD2 inhibition and its knockdown affect chromatin accessibility and prevent the upregulation of oligodendrocyte differentiation genes. Moreover, mice lacking PAD2 display motor dysfunction and a decreased number of myelinated axons in the corpus callosum. We conclude that citrullination contributes to proper oligodendrocyte lineage progression and myelination.
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