Boneva Neli, Frenkian-Cuvelier Melinee, Bidault Jocelyne, Brenner Talma, Berrih-Aknin Sonia
CNRS-UMR 8162, IPSC, Université Paris XI, Hôpital Marie Lannelongue, 133 Avenue de la Résistance, 92350 Le Plessis-Robinson, France.
J Neuroimmunol. 2006 Aug;177(1-2):119-31. doi: 10.1016/j.jneuroim.2006.05.017. Epub 2006 Jul 20.
MG with anti-MuSK antibodies (MuSK+) is often characterized with muscle atrophy and excellent response to plasma exchanges. To elucidate some MuSK+ MG features, we analyzed the functional effects of anti-MuSK Abs in human TE 671 muscle cells. We found that some MuSK+ sera induced a striking inhibition of proliferation, accompanied by: 1) cell cycle arrest, 2) atrogin-1 overexpression, 3) AChR subunits, rapsyn, Rho A and cdc42 downregulation. These effects correlated to disease severity and to anti-MuSK Abs titer and vanished following PE. Altogether, these results indicate that anti-MuSK Abs could be pathogenic by contributing to the muscle atrophy in MuSK+ MG patients.
伴有抗肌肉特异性激酶(MuSK)抗体(MuSK阳性)的重症肌无力(MG)通常表现为肌肉萎缩,且对血浆置换反应良好。为阐明一些MuSK阳性MG的特征,我们分析了抗MuSK抗体在人TE 671肌肉细胞中的功能效应。我们发现,一些MuSK阳性血清可显著抑制细胞增殖,同时伴有:1)细胞周期停滞;2)atrogin-1过表达;3)乙酰胆碱受体(AChR)亚基、rapsyn、Rho A和cdc42下调。这些效应与疾病严重程度及抗MuSK抗体滴度相关,且在血浆置换后消失。总之,这些结果表明,抗MuSK抗体可能通过导致MuSK阳性MG患者的肌肉萎缩而具有致病性。