Kazimer R M, Whisler R L, Stephens R E, Pearl D K, Yates A J
Department of Pathology, Ohio State University, Columbus 43210.
J Neurooncol. 1989 Jul;7(2):145-50. doi: 10.1007/BF00165099.
We have developed an in vitro assay for Natural Killer (NK) cell cytolysis of and binding to substrate attached human glioma and fetal brain cells. The monolayer cells were labeled with [51Cr] and the effectors were directly sedimented onto these substrate attached target cells. Using this method we screened several glioma and fetal brain cell lines. The results indicate that the majority of gliomas are NK resistant, however two of the tested lines (U251MG and BN3) were relatively sensitive as were the fetal brain cell lines (CHI and CHII). We conclude that this monolayer assay for NK cytotoxicity and binding of glioma targets is a reproducible and valid method for assessing NK sensitivity, and should have applications in the study of other cultured solid tumors and substrate attached cells.
我们开发了一种体外检测方法,用于检测自然杀伤(NK)细胞对附着于底物的人胶质瘤细胞和胎儿脑细胞的细胞溶解作用及结合情况。将单层细胞用[51Cr]标记,效应细胞直接沉淀在这些附着于底物的靶细胞上。利用这种方法,我们筛选了几种胶质瘤和胎儿脑细胞系。结果表明,大多数胶质瘤对NK有抗性,然而,两个受试细胞系(U251MG和BN3)相对敏感,胎儿脑细胞系(CHI和CHII)也是如此。我们得出结论,这种用于检测NK细胞毒性和胶质瘤靶细胞结合的单层检测方法是评估NK敏感性的一种可重复且有效的方法,应可应用于其他培养实体瘤和附着于底物的细胞的研究。