Aoki N, Maruki M, Miyazaki H, Tange T
Department of Toxicology, Tokyo Metropolitan Research Laboratory of Public Health, Japan.
Res Exp Med (Berl). 1995;195(1):39-47. doi: 10.1007/BF02576772.
We examined the protein kinase (PK) activity of the c-yes and c-src gene proteins (c-YES, c-SRC) at an early phase of 12-O-tetradecanoyl phorbol-13-acetate (TPA)-induced megakaryocytic differentiation of T-33 and K562 cells with use of immunoprecipitation and in vitro kinase assay. We found that c-SRC PK activity of TPA-treated T-33 and K562 cell lines had been enhanced compared with the untreated ones, but in contrast, no enhancement of c-YES PK activity by the TPA treatment was observed in these cell lines. We also examined PK activity in TPA-induced monocytic differentiation of U937 monoblastic cells that exhibited no megakaryocytic markers and found that both the c-YES and c-SRC PK activity was enhanced by the TPA treatment. Our data suggest that c-YES and c-SRC play different and unique roles in TPA-induced megakaryocytic differentiation in T-33 and K562 cells.
我们运用免疫沉淀法和体外激酶测定法,检测了12 - O - 十四酰佛波醇 - 13 - 乙酸酯(TPA)诱导T - 33和K562细胞向巨核细胞分化早期阶段的c - yes和c - src基因蛋白(c - YES、c - SRC)的蛋白激酶(PK)活性。我们发现,与未处理的细胞系相比,经TPA处理的T - 33和K562细胞系的c - SRC PK活性增强,但相比之下,在这些细胞系中未观察到TPA处理对c - YES PK活性有增强作用。我们还检测了TPA诱导无巨核细胞标志物的U937单核细胞向单核细胞分化过程中的PK活性,发现TPA处理可增强c - YES和c - SRC的PK活性。我们的数据表明,c - YES和c - SRC在TPA诱导的T - 33和K562细胞向巨核细胞分化过程中发挥着不同且独特的作用。