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胰岛素及胰岛素样生长因子在中国仓鼠成纤维细胞中的促有丝分裂作用和结合特性

Mitogen-potentiating action and binding characteristics of insulin and insulin-like growth factors in Chinese hamster fibroblasts.

作者信息

Van Obberghen-Schilling E, Pouysségur J

出版信息

Exp Cell Res. 1983 Sep;147(2):369-78. doi: 10.1016/0014-4827(83)90219-7.

Abstract

alpha-Thrombin alone is able to stimulate DNA synthesis reinitiation of G0-arrested Chinese hamster lung fibroblasts (CC139) as well as continued growth of these cells in serum-free medium. Although insulin at high concentrations (1-10 micrograms/ml) is not intrinsically mitogenic for these cells, it potently enhances the growth-promoting action of thrombin. The generation time of CC139 cells in the defined medium, transferrin, alpha-thrombin, insulin, is around 15 h. To determine whether this effect of insulin is mediated via putative receptors for the insulin-like growth factors (IGFs) on these cells, we examined the abilities of two IGFs, Multiplication-Stimulating Activity (MSA) and IGF-I, to potentiate the thrombin-induced reinitiation of DNA synthesis. Both IGFs were found to be as effective as insulin for this biological effect; however, much lower concentrations were required to elicit half-maximal response, 100 ng/ml of MSA and 30 ng/ml of IGF-I. Detailed binding studies using 125I-labelled insulin, MSA, and IGF-I revealed that CC139 cells specifically bind all three polypeptides with IC50 values for the corresponding ligands of 1-2 ng/ml, 80-100 ng/ml, and 30-40 ng/ml, respectively. 125I-MSA binding was insulin-insensitive, whereas insulin did compete with 125I-IGF-I for binding to CC139 cells. These results indicate that CC139 cells possess at least two types of IGF receptors, an insulin-insensitive IGF receptor with high affinity for MSA which apparently mediates its biological effect, and an insulin-sensitive IGF-I receptor. Insulin appears to exert its mitogen-potentiating activity in CC139 fibroblasts by interacting with the IGF-I receptor.

摘要

单独的α-凝血酶能够刺激G0期停滞的中国仓鼠肺成纤维细胞(CC139)重新开始DNA合成,并能使这些细胞在无血清培养基中持续生长。虽然高浓度(1 - 10微克/毫升)的胰岛素本身对这些细胞没有促有丝分裂作用,但它能显著增强凝血酶的促生长作用。在限定培养基、转铁蛋白、α-凝血酶和胰岛素存在的情况下,CC139细胞的倍增时间约为15小时。为了确定胰岛素的这种作用是否通过这些细胞上假定的胰岛素样生长因子(IGF)受体介导,我们检测了两种IGF,即促有丝分裂活性因子(MSA)和IGF-I,增强凝血酶诱导的DNA合成重新启动的能力。发现这两种IGF在这种生物学效应上与胰岛素一样有效;然而,引发半数最大反应所需的浓度要低得多,MSA为100纳克/毫升,IGF-I为30纳克/毫升。使用125I标记的胰岛素、MSA和IGF-I进行的详细结合研究表明,CC139细胞能特异性结合所有这三种多肽,相应配体的IC50值分别为1 - 2纳克/毫升、80 - 100纳克/毫升和30 - 40纳克/毫升。125I-MSA结合不受胰岛素影响,而胰岛素确实能与125I-IGF-I竞争结合CC139细胞。这些结果表明,CC139细胞至少拥有两种类型的IGF受体,一种对MSA具有高亲和力的胰岛素不敏感IGF受体,它显然介导了MSA的生物学效应,以及一种胰岛素敏感的IGF-I受体。胰岛素似乎通过与IGF-I受体相互作用在CC139成纤维细胞中发挥其促有丝分裂增强活性。

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