Salapa Hannah E, Lee Sangmin, Shin Yoojin, Levin Michael C
Department of Anatomy and Cell Biology, CMSNRC (Cameco MS Neuroscience Research Center), University of Saskatchewan, Saskatoon, SK S7N0Z1, Canada.
Veterans Administration Medical Center, Memphis, TN 38104, USA.
Brain Sci. 2017 Jun 18;7(6):69. doi: 10.3390/brainsci7060069.
Multiple sclerosis (MS) is a demyelinating, autoimmune disease of the central nervous system. In recent years, it has become more evident that neurodegeneration, including neuronal damage and axonal injury, underlies permanent disability in MS. This manuscript reviews some of the mechanisms that could be responsible for neurodegeneration and axonal damage in MS and highlights the potential role that dysfunctional heterogeneous nuclear ribonucleoprotein A1 (hnRNP A1) and antibodies to hnRNP A1 may play in MS pathogenesis.
多发性硬化症(MS)是一种中枢神经系统的脱髓鞘自身免疫性疾病。近年来,越来越明显的是,包括神经元损伤和轴突损伤在内的神经退行性变是MS永久性残疾的基础。本文综述了一些可能导致MS神经退行性变和轴突损伤的机制,并强调了功能失调的异质性核糖核蛋白A1(hnRNP A1)和抗hnRNP A1抗体在MS发病机制中可能发挥的潜在作用。