Steer M L
Ann Surg. 1975 Nov;182(5):603-9. doi: 10.1097/00000658-197511000-00012.
Many hormones interact with their target cells by binding to receptors located on the external surface of the target cells' plasma membrane and subsequently stimulating the enzyme, adenyl cyclase, which is located within the plasma membrane. Stimulation of adenyl cyclase results in formation of cyclic AMP which is released from the membrane into the cell and acts within the cell to regulate a wide variety of cellular processes. In this review, the characteristics of hormone receptors and the relationship between receptor occupancy and adenyl cyclase stimulation are discussed. Our current understanding of the roles of hormones, substrate, magnesium, calcium, and guanine nucleotides as regulators of adenyl cyclase activity is summarized. Because of the central importance of adenyl cyclase and cyclic AMP as mediators of the cellular response to hormones, it is to be expected that many diseases may result from defects in this enzyme system. Indeed, several adenyl cyclase related diseases have been identified and the molecular bases for these diseases are discussed in this review.
许多激素通过与位于靶细胞质膜外表面的受体结合,进而刺激位于质膜内的腺苷酸环化酶,与它们的靶细胞相互作用。腺苷酸环化酶的激活导致环磷酸腺苷(cAMP)的形成,cAMP从膜释放到细胞内,并在细胞内发挥作用以调节多种细胞过程。在这篇综述中,讨论了激素受体的特性以及受体占据与腺苷酸环化酶刺激之间的关系。总结了我们目前对激素、底物、镁、钙和鸟嘌呤核苷酸作为腺苷酸环化酶活性调节剂的作用的理解。由于腺苷酸环化酶和环磷酸腺苷作为细胞对激素反应的介质具有核心重要性,可以预期许多疾病可能由该酶系统的缺陷引起。事实上,已经鉴定出几种与腺苷酸环化酶相关的疾病,并且在这篇综述中讨论了这些疾病的分子基础。