Suzumura A, Lisak R P, Silberberg D H
J Neuroimmunol. 1986 Apr;11(2):137-47. doi: 10.1016/0165-5728(86)90115-3.
In order to quantitate oligodendrocyte cytotoxicity induced by sera from patients with multiple sclerosis (MS) and control sera, we established a 51Cr release assay system using cultured oligodendrocytes as target cells. With this assay system, we detected serum-induced cytotoxicity in isolated oligodendrocytes in sera from patients with MS, other neurological diseases (OND) and normal individuals. Oligodendrocytes were much more susceptible than astrocytes. The serum cytotoxicity was abolished by heating sera at either 56 degrees C or 50 degrees C for 30 min, and disappeared in storage at 23 degrees C for 1 month or at 4 degrees C for 2 months. Addition of fresh guinea pig serum as a source of complement did not restore the cytotoxic effect. Although the serum factor cytotoxic to oligodendrocytes is not specific for sera from patients with MS, it is possible that it may damage oligodendrocytes if the blood-brain barrier is impaired, as occurs in MS.
为了定量检测多发性硬化症(MS)患者血清和对照血清诱导的少突胶质细胞毒性,我们建立了一种以培养的少突胶质细胞为靶细胞的51Cr释放检测系统。利用该检测系统,我们检测了MS患者、其他神经系统疾病(OND)患者和正常个体血清中分离的少突胶质细胞的血清诱导细胞毒性。少突胶质细胞比星形胶质细胞更易受影响。血清在56℃或50℃加热30分钟后,细胞毒性消失,在23℃储存1个月或4℃储存2个月后细胞毒性也消失。添加新鲜豚鼠血清作为补体来源并不能恢复细胞毒性作用。虽然对少突胶质细胞具有细胞毒性的血清因子并非MS患者血清所特有,但如果血脑屏障受损,如在MS中发生的那样,它可能会损伤少突胶质细胞。