Localization and diffusion of glucagon receptor in rat hepatocytes.

Receptor Pub Date : 1994-01-01
S S Gupte
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Abstract

The lateral diffusion rate of glucagon receptor in rat hepatocyte plasma membrane in the absence and presence of glucagon was measured to be approximately 7.0 x 10(-10) cm2/s. The percentage of glucagon receptor molecules remaining on the cell surface after the activation of signal transduction process by 100 nM glucagon was approximately 74% of its original number. Although the number of glucagon receptors on the plasma membrane capable of interacting with its signal transduction partners decreases on addition of glucagon, the lateral diffusion rate and the percentage of mobile receptors remain essentially unchanged. A hypothesis has been developed that for signal transduction to occur, the random diffusion-dependent collision of one, two, or all three components is an essential part, and it may be the rate-limiting step. An approximate calculation has been made of random diffusion-dependent theoretical and experimental collision frequencies using experimentally measured concentrations and reasonable value for diffusion rate of G protein to investigate the role of diffusion in signal transduction. These calculations indicate that the diffusion of individual components is important and may be the rate-limiting step in the signal transduction process. The diffusion rate and percent mobile fraction of glucagon receptor data presented in this article are the first step toward elucidating the validity of the diffusion-dependent signal transduction hypothesis.

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胰高血糖素受体在大鼠肝细胞中的定位和扩散。
在胰高血糖素存在和不存在的情况下,胰高血糖素受体在大鼠肝细胞质膜中的横向扩散速率约为7.0 x 10(-10) cm2/s。100 nM胰高血糖素激活信号转导过程后,留在细胞表面的胰高血糖素受体分子百分比约为其原始数量的74%。虽然质膜上能够与其信号转导伙伴相互作用的胰高血糖素受体的数量随着胰高血糖素的加入而减少,但横向扩散速率和移动受体的百分比基本保持不变。一个假设已经发展为信号转导发生,一个,两个,或所有三个组件的随机扩散依赖碰撞是一个重要的部分,它可能是速率限制步骤。利用实验测量的G蛋白浓度和合理的扩散速率值,对随机扩散相关的理论和实验碰撞频率进行了近似计算,探讨了扩散在信号转导中的作用。这些计算表明,各个组分的扩散是重要的,可能是信号转导过程中的限速步骤。本文中提出的扩散率和胰高血糖素受体的移动百分率数据是阐明扩散依赖信号转导假说有效性的第一步。
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A modeling study of the alpha-subunit of human high-affinity receptor for immunoglobulin-E. Characterization of growth hormone-induced tyrosine-phosphorylated proteins in mouse cells that express GH receptors. Synthetic peptides derived from the steroid binding domain block modulator and molybdate action toward the rat glucocorticoid receptor. Modulation of angiotensin II receptor (AT2) mRNA levels in R3T3 cells. Growth hormone (GH)-induced tyrosine-phosphorylated proteins in cells that express GH receptors.
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