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克隆化细胞毒性T淋巴细胞介导的细胞毒性动力学

Kinetics of cellular cytotoxicity mediated by cloned cytotoxic T lymphocytes.

作者信息

Callewaert D M, Meyers P, Hiernaux J, Radcliff G

机构信息

Department of Chemistry, Oakland University, Rochester, Michigan.

出版信息

Immunobiology. 1988 Dec;178(3):203-14. doi: 10.1016/S0171-2985(88)80065-2.

Abstract

Kinetic methods can provide significant information concerning the mechanism of cellular cytotoxicity reactions. Previous kinetic studies of cytotoxic T lymphocytes (Tc) have been hampered by the heterogeneity of the effector cell population tested. We therefore examined the kinetics of lysis mediated by cloned, IL 2 and antigen-dependent murine Tc cells with strong cytotoxic activity that is restricted to distinct tumor-associated antigens on P815 mastocytoma target cells. Initial velocity measurements for cytotoxicity mediated by these clones fit a simple Michaelian kinetic model. Specific activity values obtained from these initial rate measurements are compared to those obtained for polyclonal Tc preparations, NK cells, and activated killer cells. Whereas the initial rate of lytic programming mediated by these cloned cells was very rapid, the rate of cytolysis mediated by the cloned cells decreased significantly within one hour. Since this decrease was observed over a wide range of E:T ratios, it is unlikely to result from product inhibition or a significant decrease in the concentration of unlysed target cells, but may be due to a decrease in the rate of programming and/or effector cell recycling. These results indicate that a simple Michaelian kinetic model is not adequate for tumor cell cytolysis by Tc cells in vitro.

摘要

动力学方法能够提供有关细胞毒性反应机制的重要信息。先前对细胞毒性T淋巴细胞(Tc)的动力学研究受到所测试的效应细胞群体异质性的阻碍。因此,我们研究了由克隆的、依赖白细胞介素2和抗原的具有强细胞毒性活性的小鼠Tc细胞介导的裂解动力学,这种活性仅限于P815肥大细胞瘤靶细胞上不同的肿瘤相关抗原。这些克隆介导的细胞毒性的初始速度测量符合简单的米氏动力学模型。将从这些初始速率测量中获得的比活性值与从多克隆Tc制剂、自然杀伤细胞和活化杀伤细胞中获得的值进行比较。虽然这些克隆细胞介导的裂解编程的初始速率非常快,但克隆细胞介导的细胞溶解速率在一小时内显著下降。由于在广泛的效靶比范围内都观察到了这种下降,所以这不太可能是由产物抑制或未裂解靶细胞浓度的显著降低导致的,而可能是由于编程速率和/或效应细胞再循环速率的降低。这些结果表明,简单的米氏动力学模型不足以解释体外Tc细胞对肿瘤细胞的细胞溶解作用。

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