Layers of organization of cAMP microdomains in a simple cell

被引:11
作者
Martin, A. C. L. [1 ]
Cooper, D. M. F. [1 ]
机构
[1] Univ Cambridge, Dept Pharmacol, Cambridge CB2 1PD, England
关键词
adenylate cyclase (AC); A-kinase-anchoring protein (AKAP); calmodulin; cAMP microdomain; capacitative Ca2+ entry (CCE); phosphodiesterase (PDE);
D O I
10.1042/BST0340480
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Based on a variety of single-cell measurements, the notion that cAMP microdomains exist in cells is being increasingly embraced. The cellular and molecular underpinnings of this organization are also steadily being revealed. A dependence of Ca2+-sensitive ACs (adenylate cyclases) in HEK-293 cells (human embryonic kidney cells) on capacitative Ca2+ entry is enforced by their presence in lipid rafts and protein-protein interactions. In these cells, many of the participants in the cAMP cascade, including AC, phosphodiesterase 4, cAMP-dependent protein kinase [PKA (protein kinase A)] and protein phosphatase 2A, are now seen to be involved in higher order assemblies. Moreover, the presence of Na+/H+ exchanger 1 in these domains creates a microclimate, protected against global swings in cellular pH. The Ca2+-stimulatable AC8, which is targeted to these regions, can sequester calmodulin for its own regulatory purposes. These devices are a sampling of the multiple layers of organization that are in place - even in a simple cell - to ensure faithful and economical communication of the cAMP message.
引用
收藏
页码:480 / 483
页数:4
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