Regulation and role of adenylyl cyclase isoforms

被引:516
作者
Hanoune, J [1 ]
Defer, N [1 ]
机构
[1] Hop Henri Mondor, INSERM, U99, F-94010 Creteil, France
关键词
cell physiology; mammals; signal transduction;
D O I
10.1146/annurev.pharmtox.41.1.145
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
At least nine closely related isoforms of adenylyl cyclases (ACs), the enzymes responsible for the synthesis of cyclic AMP (cAMP) from ATP, have been cloned and characterized in mammals. Depending on the properties and the relative levels of the isoforms expressed in a tissue or a cell type at a specific time, extracellular signals received through the G-protein-coupled receptors can be differentially integrated. The present review deals with various aspects of such regulations, emphasizing the role of calcium/calmodulin in activating AC1 and AC8 in the central nervous system, the potential inhibitory effect of calcium on AC5 and AC6, and the changes in the expression pattern of the isoforms during development. A particular emphasis is given to the role of cAMP during drug and ethanol dependency and to some experimental limitations (pitfalls in the interpretation of cellular transfection, scarcity of the invalidation models, existence of complex macromolecular structures, etc).
引用
收藏
页码:145 / 174
页数:30
相关论文
共 216 条
[31]   CA2+-SENSITIVE ADENYLYL CYCLASES [J].
COOPER, DMF ;
MONS, N ;
FAGAN, K .
CELLULAR SIGNALLING, 1994, 6 (08) :823-&
[32]  
COOPER DMF, 1991, BIOCHEM J, V278, P903
[33]   ADENYLYL CYCLASES AND THE INTERACTION BETWEEN CALCIUM AND CAMP SIGNALING [J].
COOPER, DMF ;
MONS, N ;
KARPEN, JW .
NATURE, 1995, 374 (6521) :421-424
[34]  
Daly JW, 1997, DRUG DEVELOP RES, V42, P98
[35]   The olfactory adenylyl cyclase type 3 is expressed in male germ cells [J].
Defer, N ;
Marinx, O ;
Poyard, M ;
Lienard, MO ;
Jégou, B ;
Hanoune, J .
FEBS LETTERS, 1998, 424 (03) :216-220
[36]   Tissue specificity and physiological relevance of various isoforms of adenylyl cyclase [J].
Defer, N ;
Best-Belpomme, M ;
Hanoune, J .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2000, 279 (03) :F400-F416
[37]   Inhibition of adenylyl cyclase by a family of newly synthesized adenine nucleoside 3'-polyphosphates [J].
Desaubry, L ;
Shoshani, N ;
Johnson, RA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (24) :14028-14034
[38]   Adenine nucleoside 3′-tetraphosphates are novel and potent inhibitors of adenylyl cyclases [J].
Désaubry, L ;
Johnson, RA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (38) :24972-24977
[39]   2',5'-dideoxyadenosine 3'-polyphosphates are potent inhibitors of adenylyl cyclases [J].
Desaubry, L ;
Shoshani, I ;
Johnson, RA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (05) :2380-2382
[40]   The interactions of adenylate cyclases with P-site inhibitors [J].
Dessauer, CW ;
Tesmer, JJG ;
Sprang, SR ;
Gilman, AG .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1999, 20 (05) :205-210