The Potential Contribution of Dysfunctional RNA-Binding Proteins to the Pathogenesis of Neurodegeneration in Multiple Sclerosis and Relevant Models

被引:16
|
作者
Libner, Cole D. [1 ,2 ]
Salapa, Hannah E. [2 ,3 ]
Levin, Michael C. [2 ,3 ]
机构
[1] Univ Saskatchewan, Dept Hlth Sci, Saskatoon, SK S7N 5A2, Canada
[2] Univ Saskatchewan, Off Saskatchewan, CMSNRC Cameco MS Neurosci Res Ctr, Multiple Sclerosis Clin Res Chair, Saskatoon, SK S7K 0M7, Canada
[3] Univ Saskatchewan, Div Neurol, Dept Med, Saskatoon, SK S7N 5A2, Canada
关键词
neurodegeneration; multiple sclerosis; RNA-binding proteins; hnRNP A1; MYELIN OLIGODENDROCYTE GLYCOPROTEIN; EPSTEIN-BARR-VIRUS; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; GREY-MATTER PATHOLOGY; STRESS GRANULES; T-CELLS; MENINGEAL INFLAMMATION; CLONAL EXPANSIONS; PHASE-SEPARATION; SARCOMA FUS;
D O I
10.3390/ijms21134571
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Neurodegeneration in multiple sclerosis (MS) is believed to underlie disease progression and permanent disability. Many mechanisms of neurodegeneration in MS have been proposed, such as mitochondrial dysfunction, oxidative stress, neuroinflammation, and RNA-binding protein dysfunction. The purpose of this review is to highlight mechanisms of neurodegeneration in MS and its models, with a focus on RNA-binding protein dysfunction. Studying RNA-binding protein dysfunction addresses a gap in our understanding of the pathogenesis of MS, which will allow for novel therapies to be generated to attenuate neurodegeneration before irreversible central nervous system damage occurs.
引用
收藏
页码:1 / 16
页数:17
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