Lederman H M, Lee J W, Gelfand E W
Clin Exp Immunol. 1985 Feb;59(2):482-90.
We have examined the identity of the T colony progenitor cell (TCPC) in T cell depleted peripheral blood mononuclear cells (PBM-E-). PBM were cultured in a limiting dilution assay utilizing PHA, T cell growth factor (TCGF) and irradiated feeder cells in semi-solid medium. The TCPC frequency was 0.10 in PBM-E+ and 0.0006 in PBM-E-. The observed TCPC frequency in PBM-E- was directly proportional to the number of contaminating PBM-E+; all of the T colonies which arose from PBM-E- could be accounted for by contaminating T cells. In other experiments, E+ cells were generated from PBM-E-, incubated in the presence of PHA and TCGF. This appearance of E+ cells could be totally abrogated by incubation with hydroxyurea. Similarly, the TCPC frequency in PBM-E- was increased by pre-incubation with PHA and TCGF, and this increase was blocked by hydroxyurea. These experiments suggest that a small number of contaminating T cells can rapidly expand in culture and that these residual T cells, not a population of pre-T cells, are the source of TCPC within the PBM-E- population.
我们已经检测了T细胞耗竭的外周血单个核细胞(PBM-E-)中T集落祖细胞(TCPC)的特性。在半固体培养基中,利用植物血凝素(PHA)、T细胞生长因子(TCGF)和经照射的饲养细胞,对PBM进行有限稀释分析培养。PBM-E+中TCPC频率为0.10,而PBM-E-中为0.0006。在PBM-E-中观察到的TCPC频率与污染的PBM-E+数量成正比;所有源自PBM-E-的T集落都可由污染的T细胞解释。在其他实验中,从PBM-E-中产生E+细胞,在PHA和TCGF存在下孵育。用羟基脲孵育可完全消除E+细胞的这种出现。同样,PBM-E-中的TCPC频率通过用PHA和TCGF预孵育而增加,且这种增加被羟基脲阻断。这些实验表明,少量污染的T细胞在培养中可迅速扩增,并且这些残留的T细胞而非前T细胞群体,是PBM-E-群体中TCPC的来源。