Yang Lei, Tan Dewei, Piao Hua
Department of Physiology, Dalian Medical University, Dalian, China.
Department of Medical Imaging, Dalian Medical University, Dalian, China.
Neurochem Res. 2016 Aug;41(8):1845-56. doi: 10.1007/s11064-016-1920-2. Epub 2016 Apr 21.
Multiple sclerosis (MS) is a multifactorial demyelinating disease characterized by neurodegenerative events and autoimmune response against myelin component. Citrullination or deimination, a post-translational modification of protein-bound arginine into citrulline, catalyzed by Ca(2+) dependent peptidylarginine deiminase enzyme (PAD), plays an essential role in physiological processes include gene expression regulation, apoptosis and the plasticity of the central nervous system, while aberrant citrullination can generate new epitopes, thus involving in the initiation and/or progression of autoimmune disorder like MS. Myelin basic protein (MBP) is the major myelin protein and is generally considered to maintain the stability of the myelin sheath. This review describes the MBP citrullination and its consequence, as well as offering further support for the "inside-out" hypothesis that MS is primarily a neurodegenerative disease with secondary inflammatory demyelination. In addition, it discusses the role of MBP citrullination in the immune inflammation and explores the potential of inhibition of PAD enzymes as a therapeutic strategy for the disease.
多发性硬化症(MS)是一种多因素导致的脱髓鞘疾病,其特征为神经退行性病变以及针对髓鞘成分的自身免疫反应。瓜氨酸化或去氨基作用,即蛋白质结合的精氨酸在钙离子依赖性肽基精氨酸脱亚氨酶(PAD)催化下转化为瓜氨酸的一种翻译后修饰,在包括基因表达调控、细胞凋亡和中枢神经系统可塑性等生理过程中发挥着重要作用,而异常的瓜氨酸化会产生新的表位,从而参与诸如MS等自身免疫性疾病的起始和/或进展。髓鞘碱性蛋白(MBP)是主要的髓鞘蛋白,通常被认为可维持髓鞘的稳定性。本综述描述了MBP的瓜氨酸化及其后果,同时为“由内而外”假说提供了进一步支持,该假说认为MS主要是一种伴有继发性炎性脱髓鞘的神经退行性疾病。此外,本文还讨论了MBP瓜氨酸化在免疫炎症中的作用,并探讨了抑制PAD酶作为该疾病治疗策略的潜力。