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生长因子和地塞米松诱导的瑞士3T3细胞中的蛋白质。与DNA合成的关系。

Growth factor- and dexamethasone-induced proteins in Swiss 3T3 cells. Relationship to DNA synthesis.

作者信息

Levenson R, Iwata K, Klagsbrun M, Young D A

出版信息

J Biol Chem. 1985 Jul 5;260(13):8056-63.

PMID:3874205
Abstract

Dexamethasone synergistically enhances the stimulation of DNA synthesis in quiescent Swiss 3T3 cells by cartilage-derived growth factor (CDGF) while having no consistent effect when added with platelet-derived growth factor (PDGF) or serum. We examined the hypothesis that this difference might be attributed to selective synthesis of individual proteins early in the G1 phase of the cell cycle. Swiss 3T3 cells were treated with CDGF, PDGF, and fetal bovine serum for 3 h, with or without dexamethasone, and [35S]methionine-labeled proteins were separated by two-dimensional electrophoresis on giant gels. Over 3300 proteins could be distinguished; 34 of these were consistently induced more than 3-fold by all three factors, while an additional 30 inductions were variably present. Dexamethasone by itself induced 8 other proteins, and at least 9 growth factor inductions were synergistically enhanced by addition of the hormone. To identify proteins intimately associated with growth control, we looked for inductions that reflected the dexamethasone synergy with CDGF on DNA synthesis and lack of such an effect with PDGF. The induction of only one group of proteins, the Band 1 isoforms (44-46 kDa, pI 6.1-5.9) displayed such selective synergy. The majority of the other growth factor inductions were inhibited by dexamethasone, even in the context of maximal DNA synthesis, implying that their increased synthesis is not required for growth. When 3T3 cells were treated with increasing doses of CDGF with and without dexamethasone, autoradiographic densities of induced proteins varied in a dose-responsive fashion. However, only levels of the Band 1 proteins bore a constant linear relationship to DNA synthesis, suggesting that they play an important role in early control of the cell cycle.

摘要

地塞米松可协同增强软骨衍生生长因子(CDGF)对静止的瑞士3T3细胞中DNA合成的刺激作用,而与血小板衍生生长因子(PDGF)或血清一起添加时则无一致的作用。我们检验了这样一种假说,即这种差异可能归因于细胞周期G1期早期个别蛋白质的选择性合成。瑞士3T3细胞用CDGF、PDGF和胎牛血清处理3小时,有或没有地塞米松,并用[35S]甲硫氨酸标记蛋白质,通过二维电泳在大型凝胶上分离。可区分出3300多种蛋白质;其中34种在所有三种因子作用下均持续诱导增加3倍以上,另外还有30种诱导作用变化不定。地塞米松本身诱导了另外8种蛋白质,并且至少9种生长因子诱导作用通过添加该激素而协同增强。为了鉴定与生长控制密切相关的蛋白质,我们寻找反映地塞米松与CDGF在DNA合成上协同作用以及与PDGF无此作用的诱导作用。只有一组蛋白质,即1带异构体(44 - 46 kDa,pI 6.1 - 5.9)的诱导表现出这种选择性协同作用。即使在最大DNA合成的情况下,大多数其他生长因子诱导作用也被地塞米松抑制,这意味着它们合成的增加并非生长所必需。当用递增剂量的CDGF处理3T3细胞,有或没有地塞米松时,诱导蛋白质的放射自显影片密度呈剂量反应方式变化。然而,只有1带蛋白质的水平与DNA合成呈恒定的线性关系,表明它们在细胞周期的早期控制中起重要作用。

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