Gusella J F, Tsiftsoglou A S, Volloch V, Weil S C, Neumann J, Housman D E
J Cell Physiol. 1982 Oct;113(1):179-85. doi: 10.1002/jcp.1041130127.
The effect of imidazole on DMSO-induced murine erythroleukemia (MEL) cell differentiation has been examined. While imidazole does inhibit heme, globin mRNA, and hemoglobin accumulation in DMSO-induced MEL cells, it does not affect the commitment of MEL cells to the specific limitation of proliferative capacity associated with the in vitro differentiation program. Furthermore, imidazole treatment does not affect DMSO-induced changes in cell volume, in the relative proportion of nuclear protein IP25, and in the specific activity of the enzyme cytidine deaminase. A clonal analysis in the presence of imidazole indicated that the drug prevents heme accumulation even in MEL cells already committed to terminal differentiation. These observations suggest that imidazole effectively dissociates two aspects of the erythroid differentiation program of MEL cells: globin gene expression and commitment to loss of proliferative capacity.
已对咪唑对二甲基亚砜(DMSO)诱导的小鼠红白血病(MEL)细胞分化的影响进行了研究。虽然咪唑确实会抑制DMSO诱导的MEL细胞中血红素、珠蛋白mRNA和血红蛋白的积累,但它并不影响MEL细胞对与体外分化程序相关的增殖能力特定限制的定向分化。此外,咪唑处理不影响DMSO诱导的细胞体积变化、核蛋白IP25的相对比例变化以及胞苷脱氨酶的比活性变化。在有咪唑存在的情况下进行的克隆分析表明,该药物即使在已经定向终末分化的MEL细胞中也能阻止血红素的积累。这些观察结果表明,咪唑有效地分离了MEL细胞红系分化程序的两个方面:珠蛋白基因表达和对增殖能力丧失的定向分化。