Watanabe T, Shafman T, Kufe D W
J Cell Physiol. 1985 Mar;122(3):435-40. doi: 10.1002/jcp.1041220314.
We have previously demonstrated that spermidine is required for proliferation and differentiation of murine Friend erythroleukemia (MEL) cells. Other studies have indicated that inhibition of MEL differentiation by dexamethasone (DEX) and 12-0-tetradecanoylphorbol-13-acetate (TPA) is reversed by the addition of exogenous polyamines. The present work has thus monitored the requirements of polyamines for induction of MEL hemoglobin synthesis by dimethyl sulfoxide. The results demonstrate that spermidine depletion inhibits induction of both heme synthesis and transcription of alpha- and beta-globin mRNA. In contrast, the results also demonstrate that polyamines are not involved in the inhibition of MEL differentiation by DEX and TPA. Thus, spermidine is required at a transcription level for induction of MEL hemoglobin synthesis, but DEX and TPA act by mechanisms other than polyamine depletion.
我们之前已经证明,亚精胺是小鼠Friend红白血病(MEL)细胞增殖和分化所必需的。其他研究表明,地塞米松(DEX)和12-0-十四烷酰佛波醇-13-乙酸酯(TPA)对MEL分化的抑制作用可通过添加外源性多胺来逆转。因此,本研究监测了多胺对二甲基亚砜诱导MEL血红蛋白合成的需求。结果表明,亚精胺耗竭会抑制血红素合成以及α-和β-珠蛋白mRNA的转录。相反,结果还表明,多胺不参与DEX和TPA对MEL分化的抑制作用。因此,亚精胺是诱导MEL血红蛋白合成所必需的转录水平的物质,但DEX和TPA的作用机制并非多胺耗竭。