Kimura A K, Wigzell H
J Immunol. 1983 May;130(5):2056-61.
In the experiments reported here, we examine the need for cell division as a critical component in the clonal expansion of alloreactive CTL precursors. Unlike previous attempts to inhibit DNA synthesis and cell division non-specifically, we have chosen to follow the normal unimpeded development of CTL in two of the most commonly used in vivo and in vitro allograft systems. The development and relative contribution of CTL lymphoblast-associated cytotoxicity has been followed by density gradient separation and functional analysis of the various fractions of lymphocytes obtained throughout the entire course of sensitization. In addition to the physical parameters (size and density), even more convincing data have been obtained from in vivo administration of 3H-TdR during the entire allograft reaction. The results presented here clearly confirm CTL precursor proliferation in vitro but provide strong evidence that in vivo CTL normally arise via a mechanism independent of blast formation and cellular proliferation. Interpretations of these findings in relationship to the concept of "clonal expansion" for the generation of mature CTL are discussed.
在本文报道的实验中,我们研究了细胞分裂作为同种异体反应性CTL前体细胞克隆扩增关键组成部分的必要性。与以往非特异性抑制DNA合成和细胞分裂的尝试不同,我们选择在两种最常用的体内和体外同种异体移植系统中追踪CTL的正常无阻碍发育。通过密度梯度分离和对整个致敏过程中获得的淋巴细胞不同组分的功能分析,追踪了CTL淋巴母细胞相关细胞毒性的发育及其相对贡献。除了物理参数(大小和密度)外,在整个同种异体移植反应期间体内给予³H-TdR还获得了更有说服力的数据。此处呈现的结果清楚地证实了CTL前体在体外的增殖,但提供了强有力的证据表明,体内CTL通常通过一种独立于母细胞形成和细胞增殖的机制产生。讨论了这些发现与成熟CTL产生的“克隆扩增”概念相关的解释。