Division of Preclinical Research, EGIS PLC, Bökényföldi út 116, 1165 Budapest, Hungary.
Mol Cell Endocrinol. 2012 Apr 28;353(1-2):3-9. doi: 10.1016/j.mce.2011.10.034. Epub 2011 Nov 9.
Signalling through adenosine 3'5' monophosphate (cAMP) is known to be important in virtually every cell. The mapping of the human genome over the past two decades has revealed an unexpected complexity of cAMP signalling, which is shared from insects to mammals. A more recent technical advance is the ability to monitor intracellular cAMP levels at subcellular spatial resolution within the time-domains of fast biochemical reactions. Thus, new light has been shed on old paradigms, some of which turn out to be multiple new ones. The novel aspects of cAMP signalling are highlighted here: (1) agonist induced plasticity - showing how the repertory of cAMP signalling genes supports homeostatic adaptation; (2) sustained cAMP signalling after endocytosis; (3) pre-assembled receptor-Gs-adenylyl cyclase complexes. Finally, a hypothetical model of propagating neuronal cAMP signals travelling form dendrites to the cell body is presented.
腺苷酸 3'5' 一磷酸(cAMP)信号通路几乎在所有细胞中都起着重要作用。在过去的二十年中,人类基因组的绘制揭示了 cAMP 信号通路的复杂程度出人意料,这种信号通路从昆虫到哺乳动物都有共享。最近的一项技术进步是能够在快速生化反应的时间范围内以亚细胞空间分辨率监测细胞内的 cAMP 水平。因此,旧的范例有了新的认识,其中一些范例实际上是新的范例。这里突出显示了 cAMP 信号的新方面:(1)激动剂诱导的可塑性-表明 cAMP 信号基因的 repertory 如何支持体内平衡的适应;(2)内吞作用后的持续 cAMP 信号;(3)预先组装的受体-Gs-腺苷酸环化酶复合物。最后,提出了一个传播神经元 cAMP 信号从树突到细胞体的假设模型。