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Spontaneous Cytotoxicity of Cultured Human Cell Lines Mediated by Normal Peripheral Blood Lymphocytes

机译:正常外周血淋巴细胞介导的培养人细胞系的自发细胞毒性

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The mechanism of spontaneous cell-mediated cytotoxicity (SCMC) of cultured cell lines has been investigated and compared with antibody-dependent cell-mediated cytotoxicity (ADCMC) by detailed kinetic analysis. the mechanism of SCMC resembles that of an enzyme, as does ADCMC where effector cells are analogous to an enzyme and the 51Cr-labeled target cells are analogous to the substrate. Temporal kinetic studies revealed an induction period of about 1 hr before significant 51Cr release for SCMC, but not for ADCMC. This induction period is not due to differences in effector-target affinity between SCMC and ADCMC.On the basis of kinetic analysis it was shown that SCMC approaches simple Michaelis-Menten enzyme kinetics, allowing determination of a Michaelis constant, Km, and maximal velocity, Vmax, for the interaction between a given effector and target cell. The Km values thus determined were found to be identical for the lysis of several target cell lines of varying SCMC susceptibility to effector cells from a given donor, whereas Vmax values for lysis of different target cells varied considerably. However, effector cells isolated from the peripheral blood of different donors exhibited different Km values for the target cells tested. Moreover, the Km value obtained for ADCMC effected by a given donor's lymphocytes was found equal to the Km value obtained for SCMC by that donor.
机译:已经研究了培养的细胞系自发细胞介导的细胞毒性(SCMC)的机制,并通过详细的动力学分析与抗体依赖性细胞介导的细胞毒性(ADCMC)进行了比较。 SCMC的机制与酶类似,ADCMC的效应细胞类似于酶,而51Cr标记的靶细胞类似于底物。时间动力学研究表明,对于SCMC而言,显着的51Cr释放之前的诱导期约为1小时,而对于ADCMC,则没有。这个诱导期不是由于SCMC和ADCMC之间的效应物-靶标亲和力的差异所致。根据动力学分析表明,SCMC接近简单的Michaelis-Menten酶动力学,可以确定Michaelis常数,Km和最大速度, Vmax,用于给定效应子和靶细胞之间的相互作用。发现如此确定的Km值对于来自给定供体的效应细胞对SCMC敏感性不同的几种靶细胞系的裂解是相同的,而对不同靶细胞的裂解的Vmax值则相差很大。但是,从不同供体外周血中分离出来的效应细胞对于测试的靶细胞表现出不同的Km值。此外,发现由给定供体的淋巴细胞影响的ADCMC获得的Km值等于该供体对SCMC获得的Km值。

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