Wong W T, Nick H S, Frost S C
Department of Biochemistry and Molecular Biology, University of Florida, Gainesville 32610.
Am J Physiol. 1992 Jan;262(1 Pt 1):C91-7. doi: 10.1152/ajpcell.1992.262.1.C91.
The differentiation of 3T3-L1 fibroblasts to adipocytes can be accelerated by the addition of 1-methyl-3-isobutylxanthine (MIX), insulin, and dexamethasone to the culture medium. During differentiation, we have demonstrated that the level of both annexin I mRNA and protein decreases. The half-times for this reduction were 2 h and 10 h for annexin I mRNA and protein, respectively. Of the added agents in the differentiation medium, only MIX caused a decline in annexin I expression in 3T3-L1 fibroblasts. The MIX effect in fibroblasts was reversible and required de novo transcription but not protein synthesis. Although MIX could be replaced by high levels of theophylline, neither agonists of the beta-adrenergic receptor nor intracellular second messengers, cAMP and cGMP, were able to reduce annexin I. The potential role of annexin I in cellular differentiation is discussed.
向培养基中添加1-甲基-3-异丁基黄嘌呤(MIX)、胰岛素和地塞米松可加速3T3-L1成纤维细胞向脂肪细胞的分化。在分化过程中,我们已经证明膜联蛋白I的mRNA和蛋白质水平均下降。膜联蛋白I的mRNA和蛋白质水平下降的半衰期分别为2小时和10小时。在分化培养基中添加的试剂中,只有MIX导致3T3-L1成纤维细胞中膜联蛋白I的表达下降。MIX对成纤维细胞的作用是可逆的,并且需要从头转录,但不需要蛋白质合成。尽管MIX可以被高浓度的茶碱替代,但β-肾上腺素能受体激动剂以及细胞内第二信使cAMP和cGMP均不能降低膜联蛋白I。本文讨论了膜联蛋白I在细胞分化中的潜在作用。