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佛波酯诱导的非T、非B白血病细胞系分化:人类淋巴祖细胞发育模型

Phorbol ester-induced differentiation of a non-T, non-B leukemic cell line: model for human lymphoid progenitor cell development.

作者信息

LeBien T W, Bollum F J, Yasmineh W G, Kersey J H

出版信息

J Immunol. 1982 Mar;128(3):1316-20.

PMID:7035564
Abstract

The phorbol ester 12-O-tetradecanoylphorbol-13-acetate (TPA) was tested for its ability to induce phenotypic changes in the human non-T,. non-B ALL cell line REH. Cells were cultured with nanogram concentrations of TPA for up to 48 hr, and were analyzed by indirect immunofluorescence with a panel of monoclonal antibodies and an antibody to the enzyme terminal deoxynucleotidyl transferase (TdT). TPA induced REH cells to express the leukemia-associated antigen, p24 (detected with monoclonal antibody BA-2; p24/BA-2) by 8 hr of culture, with induction complete by 24 hr. TPA-treated cells also underwent a concomitant decrease in the expression of TdT when analyzed enzymatically or by immunofluorescence. Analysis of TPA-treated cells with monoclonal antibodies BA-1 (detecting a B cell-associated antigen), 7.2 (detecting a monomorphic HLA-DR antigen), or OKT11 (detecting a structure closely associated with the E receptor) showed no change compared to controls. In addition there was no detectable cytoplasmic immunoglobulin in control or TPA-treated cells. These results show clearly that TPA is capable of inducing phenotypic changes in REH cells. Such changes may reflect the differentiation-linked expression of antigens present in normal bone marrow lymphoid progenitor cells.

摘要

佛波酯12 - O -十四烷酰佛波醇- 13 -乙酸酯(TPA)被用于检测其诱导人类非T、非B急性淋巴细胞白血病细胞系REH发生表型变化的能力。将细胞与纳克浓度的TPA一起培养长达48小时,并用一组单克隆抗体和一种针对末端脱氧核苷酸转移酶(TdT)的抗体通过间接免疫荧光法进行分析。培养8小时后,TPA诱导REH细胞表达白血病相关抗原p24(用单克隆抗体BA - 2检测;p24/BA - 2),24小时时诱导完成。当通过酶法或免疫荧光法分析时,经TPA处理的细胞中TdT的表达也随之降低。用单克隆抗体BA - 1(检测一种B细胞相关抗原)、7.2(检测一种单态性HLA - DR抗原)或OKT11(检测一种与E受体密切相关的结构)对经TPA处理的细胞进行分析,结果显示与对照相比没有变化。此外,在对照细胞或经TPA处理的细胞中均未检测到细胞质免疫球蛋白。这些结果清楚地表明TPA能够诱导REH细胞发生表型变化。这种变化可能反映了正常骨髓淋巴祖细胞中存在的抗原与分化相关的表达。

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