Hirsh Liron, Ben-Ami Ido, Freimann Sarit, Dantes Ada, Tajima Kimihisa, Kotsuji Fumikazu, Amsterdam Abraham
Department of Molecular Cell Biology, The Weizmann Institute of Science, Rehovot 76100, Israel.
Biochem Biophys Res Commun. 2005 Jan 7;326(1):1-6. doi: 10.1016/j.bbrc.2004.10.168.
Gonadotropic hormone, luteinizing hormone, and follicle-stimulating hormone exert their effect via activation of G-coupled receptors, which activate the hormone sensitive adenylyl cyclase, protein kinase A, and cyclic AMP responsive elements. This activation leads to specific de novo synthesis of steroidogenic factors and steroidogenic enzymes. In normal cells and following activation of this signaling pathway, desensitization period will be followed. This down-regulation, which was studied in detail for the last three decays, was found to take place at various steps of these signal transduction pathways as well as at different kinetics. A common and diverse feature of the mechanism of desensitization in other G-coupled-7-transmembrane receptor system is also discussed.
促性腺激素、黄体生成素和卵泡刺激素通过激活G偶联受体发挥作用,这些受体激活激素敏感的腺苷酸环化酶、蛋白激酶A和环磷酸腺苷反应元件。这种激活导致类固醇生成因子和类固醇生成酶的特异性从头合成。在正常细胞中以及该信号通路激活后,会进入脱敏期。在过去三十年中对这种下调进行了详细研究,发现它发生在这些信号转导通路的各个步骤以及不同的动力学过程中。还讨论了其他G偶联7跨膜受体系统脱敏机制的一个共同且多样的特征。