MacDonald H R, Lees R K
J Immunol. 1980 Mar;124(3):1308-13.
The requirement for DNA synthesis in the induction of cytolytic T lymphocytes (CTL) by alloantigens has been investigated. C57BL/6 splenic T cells purified by passage on nylon wool columns were stimulated in vitro in mixed leukocyte culture (MLC) and assayed for cytotoxicity against 51Cr-labeled target cells. With this system, CTL activity was detectable after 24 hr of MLC and reached high levels after 48 hr. Addition of cytosine arabinoside (ARA-C) or hydroxyurea to such cultures at concentrations that were sufficient to inhibit DNA synthesis by greater than 98% did not reduce CTL activity measured after 24 hr; however, the increase in activity that occurred between 24 and 48 hr in control cultures was strongly reduced (or abolished) by these drugs. Velocity sedimentation analysis of MLC cells activated for 48 hr in the presence of ARA-C further revealed that CTL precursor lymphocytes had enlarged into medium- to large-sized CTL under these conditions. These studies provide direct evidence that the primary induction of CTL by alloantigens can be dissociated into a differentiation step, which occurs within 24 hr in the absence of DNA synthesis and is accompanied by blast transformation, and a subsequent proliferation.
对同种异体抗原诱导细胞毒性T淋巴细胞(CTL)过程中DNA合成的需求进行了研究。通过尼龙毛柱传代纯化的C57BL/6脾T细胞在混合淋巴细胞培养(MLC)中进行体外刺激,并检测其对51Cr标记靶细胞的细胞毒性。在这个系统中,MLC培养24小时后可检测到CTL活性,48小时后达到高水平。在培养物中加入足以抑制DNA合成超过98%的阿糖胞苷(ARA-C)或羟基脲,在24小时时测定的CTL活性并未降低;然而,对照培养物在24至48小时之间出现的活性增加被这些药物强烈降低(或消除)。对在ARA-C存在下激活48小时的MLC细胞进行速度沉降分析进一步表明,在这些条件下,CTL前体淋巴细胞已扩增为中等至大型CTL。这些研究提供了直接证据,表明同种异体抗原对CTL的初次诱导可分为一个分化步骤,该步骤在无DNA合成的情况下24小时内发生,并伴有原始细胞转化,以及随后的增殖。