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重症肌无力免疫球蛋白对培养的大鼠肌管的补体依赖性溶解作用。

Complement-dependent lysis of cultured rat myotubes by myasthenic immunoglobulins.

作者信息

Ashizawa T, Appel S H

出版信息

Neurology. 1985 Dec;35(12):1748-53. doi: 10.1212/wnl.35.12.1748.

Abstract

We used cultured myotubes to demonstrate complement-dependent lysis of muscle membranes by serum from patients with myasthenia gravis. Lysis was monitored by light microscopy and release of incorporated [86Rb]. In the presence of guinea pig complement (GPC), 18 of 37 heat-inactivated myasthenic sera (49%), but none of 16 controls, caused morphologically detectable myotube lysis. Ten of 19 myasthenic sera (53%) increased [86Rb]-release compared with 10 controls. Immunoglobulin fractions retained the complement-dependent lytic activity. Inactivation of GPC prevented the lysis. [86Rb]-release appeared to correlate with clinical severity. The complement-dependent lysis resulted in a decrease in the number of acetylcholine receptors (AChRs) in myotubes, and AChR-immunoglobulin complexes were found in the medium of lysed cultures. The data suggest that cultured myotubes can be used to document complement-dependent antibody reactions in the pathogenesis of myasthenia.

摘要

我们使用培养的肌管来证明重症肌无力患者血清对肌膜的补体依赖性溶解作用。通过光学显微镜和掺入的[⁸⁶Rb]的释放来监测溶解情况。在豚鼠补体(GPC)存在的情况下,37份热灭活的重症肌无力血清中有18份(49%)导致了形态学上可检测到的肌管溶解,而16份对照血清均未引起这种情况。与10份对照血清相比,19份重症肌无力血清中有10份(53%)增加了[⁸⁶Rb]的释放。免疫球蛋白组分保留了补体依赖性溶解活性。GPC的灭活可防止溶解。[⁸⁶Rb]的释放似乎与临床严重程度相关。补体依赖性溶解导致肌管中乙酰胆碱受体(AChR)数量减少,并且在溶解培养物的培养基中发现了AChR - 免疫球蛋白复合物。这些数据表明,培养的肌管可用于证明重症肌无力发病机制中补体依赖性抗体反应。

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