Bradford Claire M, Ramos Inês, Cross Alison K, Haddock Gail, McQuaid Stephen, Nicholas Anthony P, Woodroofe M Nicola
Biomedical Research Centre, Sheffield Hallam University, Howard Street, S1 1WB South Yorkshire, UK.
Neuropathology Laboratory, Department of Pathology, Royal Group of Hospitals Trust, Grosvenor Road, Belfast, Northern Ireland BT12 6BL, UK.
J Neuroimmunol. 2014 Aug 15;273(1-2):85-95. doi: 10.1016/j.jneuroim.2014.05.007. Epub 2014 May 27.
Multiple sclerosis (MS) is a chronic inflammatory neurodegenerative disease, considered to be autoimmune in origin. Post-translational modification of central nervous system proteins, including glial fibrillary acidic protein (GFAP) and myelin basic protein (MBP), through citrullination of arginine residues, may lead to exposure of neoepitopes, triggering autoimmunity. Here we investigated the expression of citrullinated proteins in active MS lesions, MS normal appearing white matter and control brain white matter. We demonstrate increased citrullinated GFAP and MBP by immunohistochemistry and western blotting in areas of ongoing demyelination, suggesting a pivotal role for deimination of GFAP and MBP in MS pathogenesis MS.
多发性硬化症(MS)是一种慢性炎症性神经退行性疾病,被认为起源于自身免疫。通过精氨酸残基的瓜氨酸化对中枢神经系统蛋白进行翻译后修饰,包括胶质纤维酸性蛋白(GFAP)和髓鞘碱性蛋白(MBP),可能会导致新表位的暴露,从而引发自身免疫。在此,我们研究了瓜氨酸化蛋白在活动性MS病灶、MS正常外观白质和对照脑白质中的表达。我们通过免疫组织化学和蛋白质印迹法证明,在正在进行脱髓鞘的区域,瓜氨酸化的GFAP和MBP有所增加,这表明GFAP和MBP的去酰胺化在MS发病机制中起关键作用。