Amri E Z, Barbaras R, Doglio A, Dani C, Grimaldi P, Ailhaud G
Biochem J. 1986 Oct 15;239(2):363-70. doi: 10.1042/bj2390363.
Confluent Ob1771 cells treated with an inhibitor of spermidine and spermine synthesis, methylglyoxyal bis(guanylhydrazone), were dependent on putrescine addition for the expression of glycerol-3-phosphate dehydrogenase and acyl-CoA synthetase, which behaved as late markers of adipose conversion. A similar dependence was observed with drug-treated Ob17MT18 and 3T3-F442A preadipocyte cells, but not with non-differentiating 3T3-C2 cells. Studies in drug-treated Ob1771 cells at the mRNA level showed that the parallel expression of mRNAs encoding for glycerol-3-phosphate dehydrogenase and an homologue of serine proteinases of Mr 28,000 [Cook, Groves, Min & Spiegelman (1985) Proc. Natl. Acad. Sci. U.S.A. 82, 6480-6484] was also dependent on putrescine addition. Double-isotope experiments with [14C]putrescine and [3H]spermidine, as well as analysis of the polyamine content in drug-treated Ob1771 cells under various conditions, demonstrate after putrescine addition that the expression of late markers of adipose conversion was highly correlated with a 2-fold increase in the intracellular concentration of spermidine. No correlation was observed with changes in the intracellular concentrations of putrescine and spermine. Long-term exposure of untreated Ob1771 cells to growth hormone, which led to the expression of late markers of adipose conversion [Doglio, Dani, Grimaldi & Ailhaud (1986) Biochem. J. 238, 123-129] was also accompanied by the same increase in spermidine concentration, which attained values identical with those determined in drug-treated cells supplemented with putrescine. This observation suggests that the permissive effect of growth hormone on the terminal differentiation of adipose cells might e related to changes in the intracellular concentration of spermidine.
用亚精胺和精胺合成抑制剂甲基乙二醛双(脒腙)处理融合的Ob1771细胞,其甘油-3-磷酸脱氢酶和酰基辅酶A合成酶的表达依赖于腐胺的添加,这两种酶是脂肪转化的晚期标志物。在用药物处理的Ob17MT18和3T3-F442A前脂肪细胞中观察到类似的依赖性,但在未分化的3T3-C2细胞中未观察到。在mRNA水平上对用药物处理的Ob1771细胞进行的研究表明,编码甘油-3-磷酸脱氢酶和28000 Mr丝氨酸蛋白酶同系物的mRNA的平行表达也依赖于腐胺的添加[库克、格罗夫斯、明和斯皮格尔曼(1985年)《美国国家科学院院刊》82,6480 - 6484]。用[14C]腐胺和[3H]亚精胺进行的双同位素实验,以及在各种条件下对用药物处理的Ob1771细胞中多胺含量的分析表明,添加腐胺后,脂肪转化晚期标志物的表达与亚精胺细胞内浓度增加2倍高度相关。未观察到与腐胺和精胺细胞内浓度变化的相关性。未处理的Ob1771细胞长期暴露于生长激素,导致脂肪转化晚期标志物的表达[多利奥、达尼、格里马尔迪和艾洛德(1986年)《生物化学杂志》238,123 - 129],同时亚精胺浓度也有相同程度的增加,其达到的值与在添加腐胺的药物处理细胞中测定的值相同。这一观察结果表明,生长激素对脂肪细胞终末分化的允许作用可能与亚精胺细胞内浓度的变化有关。