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胰岛素在生长激素刺激的3T3细胞脂肪生成中的作用。

Role of insulin in growth hormone-stimulated 3T3 cell adipogenesis.

作者信息

Guller S, Corin R E, Mynarcik D C, London B M, Sonenberg M

机构信息

Memorial Sloan-Kettering Cancer Center, New York, New York 10021.

出版信息

Endocrinology. 1988 May;122(5):2084-9. doi: 10.1210/endo-122-5-2084.

Abstract

The role of insulin during GH-stimulated adipogenesis of 3T3-F442A fibroblasts was investigated. Adipogenesis in defined medium (DM), as quantified by the level of glycerol-3-phosphate dehydrogenase activity, revealed that there existed a strict requirement for both insulin and GH during adipogenesis. The concentration of insulin required to elicit half-maximal adipogenesis was approximately 20 nM. Insulin-like growth factor I was less effective than insulin in promoting adipogenesis, indicating that insulin action during differentiation was most likely mediated through the insulin receptor. Cellular viability was not compromised by the absence of insulin, as judged by colony-forming efficiency or trypan blue exclusion. Deletion of insulin from DM supplemented with 1 nM recombinant human GH reduced glycerol-3-phosphate dehydrogenase activity to uninduced levels. Removal of other individual DM constituents did not have this effect. The growth factors fibroblast growth factor, platelet-derived growth factor, and bombesin did not substitute for insulin during GH-stimulated adipogenesis. The characteristic increase in cell number observed during serum-based differentiation, reflecting clonal expansion of young adipocytes, did not occur in DM supplemented with insulin, and insulin-like growth factor I were necessary for this event. These results suggest that insulin functions in concert with GH as a coinducer of the differentiating signals.

摘要

研究了胰岛素在生长激素(GH)刺激3T3-F442A成纤维细胞脂肪生成过程中的作用。通过甘油-3-磷酸脱氢酶活性水平定量测定限定培养基(DM)中的脂肪生成,结果显示脂肪生成过程中对胰岛素和生长激素均有严格需求。引发半数最大脂肪生成所需的胰岛素浓度约为20 nM。胰岛素样生长因子I在促进脂肪生成方面不如胰岛素有效,这表明分化过程中的胰岛素作用很可能是通过胰岛素受体介导的。根据集落形成效率或台盼蓝排斥法判断,缺乏胰岛素时细胞活力并未受损。从添加1 nM重组人生长激素的DM中去除胰岛素会使甘油-3-磷酸脱氢酶活性降至未诱导水平。去除其他单独的DM成分则没有这种效果。在GH刺激的脂肪生成过程中,成纤维细胞生长因子、血小板衍生生长因子和蛙皮素等生长因子不能替代胰岛素。在基于血清的分化过程中观察到的细胞数量特征性增加反映了年轻脂肪细胞的克隆扩增,在添加胰岛素和胰岛素样生长因子I的DM中并未出现这种情况,而这两种物质对此过程是必需的。这些结果表明,胰岛素与GH协同作用,作为分化信号的共诱导剂。

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