激素调控的分子方面

K. Siddle, G. Brierley
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引用次数: 0

摘要

激素在血液中流动,对目标组织产生影响,这些组织在解剖学上往往远离激素分泌的部位。它们通过结合和激活通常具有高度选择性或特异性的受体来实现这一目标。受体根据其分子结构和作用机制可分为几个科。在内分泌学中重要的常见受体包括细胞表面g蛋白偶联受体、酪氨酸激酶受体、细胞因子样受体和细胞核内激素受体。在这一章中,描述了这些受体发出的信号通路的基本解剖结构,并讨论了信息编码和传递的原理和机制,以及这些在内分泌疾病中是如何出错的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular Aspects of Hormone Regulation
Hormones travel in the bloodstream to exert effects on target tissues, which are often anatomically remote from the site of hormone secretion. They achieve this by binding and activating receptors, which usually are highly selective or specific. Receptors are grouped into several families according to their molecular structure and mechanism of action. Common classes of receptors important in endocrinology include cell surface G-protein-coupled receptors, receptor tyrosine kinases, and cytokine-like receptors, and intracellular nuclear hormone receptors. In this chapter the basic anatomy of the signalling pathways emanating from these receptors is described, and the principles and mechanisms of information coding and transmission, and how these may go awry in endocrine disease, are discussed.
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