Published February 26, 2004 | Version v1
Journal article

Genoprotective pathways Part I. Extracellular signaling through Gs protein-coupled adenosine receptors prevents oxidative DNA damage

Description

Adenosine has been previously shown to be a cytoprotective paracrine released by injured cells. However, it is presently unknown whether extracellular adenosine can prevent DNA damage. We show here that the adenosine analog, 2-chloroadenosine (2CA), has a potent (IC50=2.04x10-9 M) genoprotective effect in cells subsequently exposed to H2O2. The genoprotective signaling is transduced through adenosine receptors of the A2a and A2b subtypes. Increasing [cAMP]i by forskolin or by cell permeable 8-br-cAMP produced a similar effect, whereas inhibiting the cAMP-mediated pathway with H-89, or increasing [nitric oxide]i or [cGMP]i blocked 2CA effect. Proteasomal inhibitors had no impact on 2CA signaling, while lithium chloride, an inhibitor of glycogen synthase kinase 3β, completely blocked 2CA-induced genoprotective effect. These data indicate for the first time that extracellular adenosine protects cells against imminent oxidative DNA damage and suggest that prophylactic activation of this pathway prior to genotoxic challenges might reduce mutation rates

Additional details

Identifiers

DOI
10.1016/j.mrfmmm.2003.11.003;
PII
S0027510703002938;

Publishing Information

Journal Title
Mutation Research
Journal Volume
546
Journal Issue
1-2
Journal Page Range
p. 93-102
ISSN
0027-5107

INIS

Country of Publication
Netherlands
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
36096576
Subject category
S60: APPLIED LIFE SCIENCES;
Descriptors DEI
ADENOSINE; AMP; DNA DAMAGES; GLYCOGEN; HYDROGEN PEROXIDE; MUTATIONS; NITRIC OXIDE; RECEPTORS
Descriptors DEC
CARBOHYDRATES; CHALCOGENIDES; HYDROGEN COMPOUNDS; MEMBRANE PROTEINS; NITROGEN COMPOUNDS; NITROGEN OXIDES; NUCLEOSIDES; NUCLEOTIDES; ORGANIC COMPOUNDS; OXIDES; OXYGEN COMPOUNDS; PEROXIDES; POLYSACCHARIDES; PROTEINS; RIBOSIDES; SACCHARIDES

Optional Information

Copyright
Copyright (c) 2003 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.