Chun P W, Kim J D, Lee C W, Shireman R B, Cantarini W F
J Biol Chem. 1984 Feb 25;259(4):2161-5.
A theoretical model for insulin receptor synthesis and degradation in differentiating 3T3-L1 adipocytes is described. This three-step irreversible ordered sequence model explains the up- and down-regulation of receptors in terms of the level of insulin concentration. Kinetic expressions were derived for the model. Numerical solutions for these equations, based on data reported by Reed and Lane (Reed, B.C., and Lane, M. D. (1980) Proc. Natl. Acad. Sci. U.S.A. 77, 285-289) were used for computer-generated curves illustrating insulin-dependent receptor synthesis and degradation. Results show that this model provides the best fit to the reported data and lend support to the suggestion that the free recycled receptor may differ from the newly synthesized receptor. A possible role for the recycled receptor in signal modulation is suggested.
本文描述了一个用于解释3T3-L1脂肪细胞分化过程中胰岛素受体合成与降解的理论模型。这个三步不可逆有序序列模型根据胰岛素浓度水平解释了受体的上调和下调。推导了该模型的动力学表达式。基于里德和莱恩报告的数据(里德,B.C.,和莱恩,M.D.(1980年)《美国国家科学院院刊》77卷,285 - 289页),对这些方程进行了数值求解,用于生成说明胰岛素依赖性受体合成和降解的计算机曲线。结果表明,该模型与报告的数据拟合度最佳,并支持了游离循环受体可能与新合成受体不同的观点。文中还提出了循环受体在信号调节中的可能作用。