Cyclic AMP: master regulator of innate immune cell function.

Abstract:

:Cyclic adenosine monophosphate (cAMP) was the original "second messenger" to be discovered. Its formation is promoted by adenylyl cyclase activation after ligation of G protein-coupled receptors by ligands including hormones, autocoids, prostaglandins, and pharmacologic agents. Increases in intracellular cAMP generally suppress innate immune functions, including inflammatory mediator generation and the phagocytosis and killing of microbes. The importance of the host cAMP axis in regulating antimicrobial defense is underscored by the fact that microbes have evolved virulence-enhancing strategies that exploit it. Many clinical situations that predispose to infection are associated with increases in cAMP, and therapeutic strategies to interrupt cAMP generation or actions have immunostimulatory potential. This article reviews the anatomy of the cAMP axis, the mechanisms by which it controls phagocyte immune function, microbial strategies to dysregulate it, and its clinical relevance.

authors

Serezani CH,Ballinger MN,Aronoff DM,Peters-Golden M

doi

10.1165/rcmb.2008-0091TR

subject

Has Abstract

pub_date

2008-08-01 00:00:00

pages

127-32

issue

2

eissn

1044-1549

issn

1535-4989

pii

2008-0091TR

journal_volume

39

pub_type

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