Okabe M, Kunieda Y, Shoji M, Nakane S, Kurosawa M, Tanaka J, Hansen S R, Asaka M
Third Department of Internal Medicine, Hokkaido University School of Medicine, Sapporo, Japan.
Leuk Res. 1995 Dec;19(12):933-43. doi: 10.1016/0145-2126(95)00039-9.
We investigated megakaryocytic differentiation in a newly-established Ph1-positive leukemic cell line, MC3, which showed tri-lineage immunophenotypes (myeloid antigens2+, CD19(1+) and CD41a1+) and was positive for CD34 and CD38. TPA induced MC3 cells to differentiate to an early stage of megakaryocyte lineage exhibiting an increase in the expression of platelet glycoproteins (GP) IIb/IIIa (CD41a), and an increase in cell size and nuclear ploidy. TPA treatment also enhanced the expression of GPIIb mRNA, and induced the expression of interleukin-6 (IL-6) and its receptor mRNAs, while it did not induce transcripts of the genes IL-11 and mpl ligand, and further decreased the transcript of the mpl gene. Consistent with these findings, MC3 cells treated with TPA showed an increased expression of GATA-1, but not GATA-3 transcripts, whereas those without TPA treatment expressed only the GATA-2 transcript. These results provide an insight into the study for the regulatory mechanism of megakaryocytopoiesis and leukemic cell differentiation.
我们研究了一种新建立的Ph1阳性白血病细胞系MC3中的巨核细胞分化情况,该细胞系表现出三系免疫表型(髓系抗原2 +、CD19(1 +)和CD41a1 +),且CD34和CD38呈阳性。佛波酯(TPA)诱导MC3细胞分化至巨核细胞系的早期阶段,表现为血小板糖蛋白(GP)IIb/IIIa(CD41a)表达增加,细胞大小和核倍性增加。TPA处理还增强了GPIIb mRNA的表达,诱导了白细胞介素-6(IL-6)及其受体mRNA的表达,而未诱导IL-11和mpl配体基因的转录本,且进一步降低了mpl基因的转录本。与这些发现一致,用TPA处理的MC3细胞GATA-1的表达增加,但GATA-3转录本未增加,而未用TPA处理的细胞仅表达GATA-2转录本。这些结果为巨核细胞生成和白血病细胞分化的调控机制研究提供了思路。