Chantel Mastos, Xiaomeng Xu, Alastair C Keen, Michelle L Halls
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引用次数: 0
Abstract
The concept of G protein-coupled receptors initially arose from studies of the β-adrenoceptor, adenylyl cyclase, and cAMP signalling pathway. Since then both canonical G protein-coupled receptor signalling pathways and emerging paradigms in receptor signalling have been defined by experiments focused on adrenoceptors. Here, we discuss the evidence for G protein coupling specificity of the nine adrenoceptor subtypes. We summarise the ability of each of the adrenoceptors to activate proximal signalling mediators including cAMP, calcium, mitogen-activated protein kinases, and protein kinase C pathways. Finally, we highlight the importance of precise spatial and temporal control of adrenoceptor signalling that is controlled by the localisation of receptors at intracellular membranes and in larger protein complexes.
G 蛋白偶联受体的概念最初产生于对β-肾上腺素受体、腺苷酸环化酶和 cAMP 信号通路的研究。此后,以肾上腺素受体为重点的实验确定了典型的 G 蛋白偶联受体信号通路和新的受体信号范式。在此,我们讨论了九种肾上腺素受体亚型的 G 蛋白偶联特异性证据。我们总结了每种肾上腺素受体激活近端信号介质的能力,包括 cAMP、钙、丝裂原活化蛋白激酶和蛋白激酶 C 通路。最后,我们强调了肾上腺素受体信号在空间和时间上精确控制的重要性,这种控制是通过受体在细胞内膜和更大的蛋白复合物中的定位来实现的。
期刊介绍:
The Handbook of Experimental Pharmacology is one of the most authoritative and influential book series in pharmacology. It provides critical and comprehensive discussions of the most significant areas of pharmacological research, written by leading international authorities. Each volume in the series represents the most informative and contemporary account of its subject available, making it an unrivalled reference source.