Drug Discovery Biology Theme, Monash Institute of Pharmaceutical Sciences, Monash University, Parkville, 3052, Victoria, Australia.
Department of Pharmacology, University of Cambridge, Tennis Court Road, Cambridge CB2 1PD, UK.
Pharmacol Ther. 2017 Apr;172:171-180. doi: 10.1016/j.pharmthera.2017.01.001. Epub 2017 Jan 26.
Signalling pathways involving the vital second messanger, cAMP, impact on most significant physiological processes. Unsurprisingly therefore, the activation and regulation of cAMP signalling is tightly controlled within the cell by processes including phosphorylation, the scaffolding of protein signalling complexes and sub-cellular compartmentalisation. This inherent complexity, along with the highly conserved structure of the catalytic sites among the nine membrane-bound adenylyl cyclases, presents significant challenges for efficient inhibition of cAMP signalling. Here, we will describe the biochemistry and cell biology of the family of membrane-bound adenylyl cyclases, their organisation within the cell, and the nature of the cAMP signals that they produce, as a prelude to considering how cAMP signalling might be perturbed. We describe the limitations associated with direct inhibition of adenylyl cyclase activity, and evaluate alternative strategies for more specific targeting of adenylyl cyclase signalling. The inherent complexity in the activation and organisation of adenylyl cyclase activity may actually provide unique opportunities for selectively targeting discrete adenylyl cyclase functions in disease.
涉及重要第二信使 cAMP 的信号通路对大多数重要的生理过程都有影响。因此,cAMP 信号的激活和调节在细胞内受到严格控制,包括磷酸化、蛋白质信号复合物的支架和亚细胞区室化等过程。这种内在的复杂性,以及九种膜结合腺苷酸环化酶之间催化位点的高度保守结构,为有效抑制 cAMP 信号带来了重大挑战。在这里,我们将描述膜结合腺苷酸环化酶家族的生物化学和细胞生物学特性,它们在细胞内的组织方式,以及它们产生的 cAMP 信号的性质,作为考虑如何干扰 cAMP 信号的前奏。我们描述了直接抑制腺苷酸环化酶活性所带来的限制,并评估了更具体地靶向腺苷酸环化酶信号的替代策略。腺苷酸环化酶活性的激活和组织的内在复杂性实际上可能为在疾病中选择性地针对离散的腺苷酸环化酶功能提供独特的机会。