Zippin Jonathan H, Chen Yanqiu, Nahirney Patrick, Kamenetsky Margarita, Wuttke Mark S, Fischman Donald A, Levin Lonny R, Buck Jochen
Department of Pharmacology, Joan and Sanford I. Weill Medical College of Cornell University, New York, New York 10021, USA.
FASEB J. 2003 Jan;17(1):82-4. doi: 10.1096/fj.02-0598fje. Epub 2002 Nov 15.
Intracellular targets of the ubiquitous second messenger cAMP are located at great distances from the most widely studied source of cAMP, the G protein responsive transmembrane adenylyl cyclases. We previously identified an alternative source of cAMP in mammalian cells lacking transmembrane spanning domains, the "soluble" adenylyl cyclase (sAC). We now demonstrate that sAC is distributed in specific subcellular compartments: mitochondria, centrioles, mitotic spindles, mid-bodies, and nuclei, all of which contain cAMP targets. Distribution at these intracellular sites proves that adenylyl cyclases are in close proximity to all cAMP effectors, suggesting a model in which local concentrations of cAMP are regulated by individual adenylyl cyclases targeted to specific microdomains throughout the cell.
普遍存在的第二信使环磷酸腺苷(cAMP)的细胞内靶点,与研究最为广泛的cAMP来源——G蛋白反应性跨膜腺苷酸环化酶,距离甚远。我们之前在缺乏跨膜结构域的哺乳动物细胞中,鉴定出了cAMP的另一种来源,即“可溶性”腺苷酸环化酶(sAC)。我们现在证明,sAC分布于特定的亚细胞区室:线粒体、中心粒、有丝分裂纺锤体、中间体和细胞核,所有这些区室都含有cAMP靶点。在这些细胞内位点的分布证明,腺苷酸环化酶与所有cAMP效应器紧密相邻,这提示了一种模型,即cAMP的局部浓度由靶向细胞内特定微结构域的单个腺苷酸环化酶调控。