Kees U R
Leukaemia Research Laboratory, Princess Margaret Hospital for Children, Perth, Australia.
Blood. 1988 Nov;72(5):1524-9.
We show here that a human leukemic cell line, PER-117, bearing the markers of a T-cell precursor phenotype, can be induced to express receptors for interleukin-2 (IL-2). These IL-2 receptors could be demonstrated to mediate a physiologic response to the lymphokine for which the high-affinity form of the IL-2 receptor appears to be essential. The phenotype of PER-117 cells corresponds to the earliest identifiable stage of T-cell differentiation, which is defined by the lack of the T3-T-cell receptor complex and the presence of the 40 Kd protein recognized by monoclonal antibodies of the CD7 group. Further evidence for the clonality and T-cell lineage of this cell line was obtained by analysis of rearrangements of genes for the T-cell receptor (TCR) beta chain and for the immunoglobulin heavy-chain (IgJH) genes. PER-117 cells could be shown to have rearranged TCR beta genes but no rearrangement of the IgJH genes. Cell line PER-117 provides a model to investigate the requirements for induction of IL-2 receptors in a cell expressing the first T-cell-specific marker and may help to elucidate the role of IL-2 during thymic differentiation and in the uncontrolled proliferation of T-cell leukemias.
我们在此表明,一种具有T细胞前体表型标志物的人白血病细胞系PER-117,可被诱导表达白细胞介素-2(IL-2)受体。这些IL-2受体可被证明介导了对该淋巴因子的生理反应,而IL-2受体的高亲和力形式似乎对此至关重要。PER-117细胞的表型对应于T细胞分化的最早可识别阶段,其定义为缺乏T3-T细胞受体复合物以及存在被CD7组单克隆抗体识别的40 Kd蛋白。通过分析T细胞受体(TCR)β链基因和免疫球蛋白重链(IgJH)基因的重排,获得了该细胞系克隆性和T细胞谱系的进一步证据。PER-117细胞可被证明具有重排的TCRβ基因,但IgJH基因未重排。细胞系PER-117提供了一个模型,用于研究在表达首个T细胞特异性标志物的细胞中诱导IL-2受体的条件,并可能有助于阐明IL-2在胸腺分化以及T细胞白血病失控增殖过程中的作用。