Sasaki D, Kosunago S, Mikami T, Matsumoto T, Suzuki M
Department of Microbiology, Tohoku College of Pharmacy, Sendai, Japan.
Biol Pharm Bull. 1993 Oct;16(10):1054-6. doi: 10.1248/bpb.16.1054.
Two subclones (K562-L and -H) were previously isolated from K562 human leukemic cells according to hemoglobin production: K562-L was expressed in less than 5% and K562-H in more than 90% of dianisidine positive cells. 12-O-Tetradecanoylphorbol-13- acetate (TPA) suppressed the expression of the erythrocytic (glycophorin A) and myelocytic (CD11b) antigens in K562-L, but increased the expression of these antigens in K562-H. TPA increased the megakaryocytic (CD61) antigens in both cells. These findings suggest that there are distinct TPA responsible factors in K562-L and -H on the expression of the erythrocytic and myelocytic antigens.
先前根据血红蛋白产生情况从K562人白血病细胞中分离出两个亚克隆(K562-L和-H):在不到5%的联茴香胺阳性细胞中表达K562-L,在超过90%的联茴香胺阳性细胞中表达K562-H。12-O-十四烷酰佛波醇-13-乙酸酯(TPA)抑制K562-L中红细胞(血型糖蛋白A)和髓细胞(CD11b)抗原的表达,但增加K562-H中这些抗原的表达。TPA增加了两种细胞中的巨核细胞(CD61)抗原。这些发现表明,K562-L和-H中存在不同的TPA相关因子,影响红细胞和髓细胞抗原的表达。