• This record comes from PubMed

Expression of Drosophila adenosine deaminase in immune cells during inflammatory response

. 2011 Mar 11 ; 6 (3) : e17741. [epub] 20110311

Language English Country United States Media electronic

Document type Journal Article, Research Support, Non-U.S. Gov't

Extra-cellular adenosine is an important regulator of inflammatory responses. It is generated from released ATP by a cascade of ectoenzymes and degraded by adenosine deaminase (ADA). There are two types of enzymes with ADA activity: ADA1 and ADGF/ADA2. ADA2 activity originates from macrophages and dendritic cells and is associated with inflammatory responses in humans and rats. Drosophila possesses a family of six ADGF proteins with ADGF-A being the main regulator of extra-cellular adenosine during larval stages. Herein we present the generation of a GFP reporter for ADGF-A expression by a precise replacement of the ADGF-A coding sequence with GFP using homologous recombination. We show that the reporter is specifically expressed in aggregating hemocytes (Drosophila immune cells) forming melanotic capsules; a characteristic of inflammatory response. Our vital reporter thus confirms ADA expression in sites of inflammation in vivo and demonstrates that the requirement for ADA activity during inflammatory response is evolutionary conserved from insects to vertebrates. Our results also suggest that ADA activity is achieved specifically within sites of inflammation by an uncharacterized post-transcriptional regulation based mechanism. Utilizing various mutants that induce melanotic capsule formation and also a real immune challenge provided by parasitic wasps, we show that the acute expression of the ADGF-A protein is not driven by one specific signaling cascade but is rather associated with the behavior of immune cells during the general inflammatory response. Connecting the exclusive expression of ADGF-A within sites of inflammation, as presented here, with the release of energy stores when the ADGF-A activity is absent, suggests that extra-cellular adenosine may function as a signal for energy allocation during immune response and that ADGF-A/ADA2 expression in such sites of inflammation may regulate this role.

See more in PubMed

Bours MJ, Swennen EL, Di Virgilio F, Cronstein BN, Dagnelie PC. Adenosine 5′-triphosphate and adenosine as endogenous signaling molecules in immunity and inflammation. Pharmacol Ther. 2006;112(2):358–404. PubMed

Aldrich MB, Blackburn MR, Kellems RE. The importance of Adenosine deaminase for lymphocyte development and function. Biochem Biophys Res Commun. 2000;272:311–315. PubMed

Franco R, Casado V, Ciruela F, Saura C, Mallol J, et al. Cell surface adenosine deaminase: much more than an ectoenzyme. Prog Neurobiol. 1997;52:283–294. PubMed

Ratech H, Thorbecke GJ, Meredith G, Hirschhorn R. Comparison and possible homology of isozymes of adenosine deaminase in Aves and humans. Enzyme. 1981;26(2):74–84. PubMed

Zavialov AV, Engström A. Human ADA2 belongs to a new family of growth factors with adenosine deaminase activity. Biochem J. 2005;391(Pt 1):51–57. PubMed PMC

Niedzwicki JG, Abernethy DR. Structure-activity relationship of ligands of human plasma adenosine deaminase2. Biochem Pharmacol. 1991;41(11):1615–1624. PubMed

Valdés L, Pose A, San José E, Martinez Vázquez JM. Tuberculous pleural effusions. Eur J Intern Med. 2003;14(2):77–88. PubMed

Niedzwicki JG, Mayer KH, Abushanab E, Abernethy DR. Plasma adenosine deaminase2 is a marker for human immunodeficiency virus-1 seroconversion. Am J Hematol. 1991;37(3):152–155. PubMed

Conlon BA, Law WR. Macrophages are a source of extra-cellular adenosine deaminase-2 during inflammatory responses. Clin Exp Immunol. 2004;138(1):14–20. PubMed PMC

Zavialov AV, Gracia E, Glaichenhaus N, Franco R, Zavialov AV, et al. Human adenosine deaminase 2 induces differentiation of monocytes into macrophages and stimulates proliferation of T helper cells and macrophages. J Leukoc Biol. 2010;88(2):279–290. PubMed

Homma K, Matsushita T, Natori S. Purification, characterization, and cDNA cloning of a novel growth factor from the conditioned medium of NIH-Sape-4, an embryonic cell line of Sarcophaga peregrina (flesh fly). J Biol Chem. 1996;271:13770–13775. PubMed

Zurovec M, Dolezal T, Gazi M, Pavlova E, Bryant PJ. Adenosine deaminase-related growth factors stimulate cell proliferation in Drosophila by depleting extra-cellular adenosine. Proc Natl Acad Sci USA. 2002;99:4403–4408. PubMed PMC

Zavialov AV, Yu X, Spillmann D, Lauvau G, Zavialov AV. Structural basis for the growth factor activity of human adenosine deaminase ADA2. J Biol Chem. 2010;285(16):12367–12377. PubMed PMC

Dolezal T, Dolezelova E, Zurovec M, Bryant PJ. A role for adenosine deaminase in Drosophila larval development. Plos Biol. 2005;3:e201. PubMed PMC

Evans CJ, Hartenstein V, Banerjee U. Thicker than blood: conserved mechanisms in Drosophila and vertebrate hematopoiesis. Dev Cell. 2003;5(5):673–690. PubMed

Babcock DT, Brock AR, Fish GS, Wang Y, Perrin L, et al. Circulating blood cells function as a surveillance system for damaged tissue in Drosophila larvae. Proc Natl Acad Sci U S A. 2008;105(29):10017–10022. PubMed PMC

Cerenius L, Lee BL, Söderhäll K. The proPO-system: pros and cons for its role in invertebrate immunity. Trends Immunol. 2008;29(6):263–271. PubMed

Li X, Zhao X, Fang Y, Jiang X, Duong T, et al. Generation of destabilized green fluorescent protein as a transcription reporter. J Biol Chem. 1998;273:34970–34975. PubMed

Rong YS, Golic KG. Gene targeting by homologous recombination in Drosophila. Science. 2000;288:2013–2018. PubMed

Qiu P, Pan PC, Govind S. A role for the Drosophila Toll/Cactus pathway in larval hematopoiesis. Development. 1998;125:1909–1920. PubMed

Harrison DA, Binari R, Nahreini TS, Gilman M, Perrimon N. Activation of a Drosophila Janus kinase (JAK) causes hematopoietic neoplasia and developmental defects. EMBO J. 1995;14(12):2857–2865. PubMed PMC

Lanot R, Zachary D, Holder F, Meister M. Postembryonic hematopoiesis in Drosophila. Dev Biol. 2001;230(2):243–257. PubMed

Rong YS, Golic KG. A targeted gene knockout in Drosophila. Genetics. 2001;157:1307–1312. PubMed PMC

Carroll D, Beumer KJ, Morton JJ, Bozas A, Trautman JK. Gene targeting in Drosophila and Caenorhabditis elegans with zinc-finger nucleases. Methods Mol Biol. 2008;435:63–77. PubMed

Ejsmont RK, Sarov M, Winkler S, Lipinski KA, Tomancak P. A toolkit for high-throughput, cross-species gene engineering in Drosophila. Nat Methods. 2009;6(6):435–437. PubMed

Zuberova M, Fenckova M, Simek P, Janeckova L, Dolezal T. Increased extra-cellular adenosine in Drosophila that are deficient in adenosine deaminase activates a release of energy stores leading to wasting and death. Dis Model Mech. 2010;3(11–12):773–784. PubMed

Sankar N, Machado J, Abdulla P, Hilliker AJ, Coe IR. Comparative genomic analysis of equilibrative nucleoside transporters suggests conserved protein structure despite limited sequence identity. Nucleic Acids Res. 2002;30:4339–4350. PubMed PMC

Rieder R, Lang K, Graber D, Micura R. Ligand-induced folding of the adenosine deaminase A-riboswitch and implications on riboswitch translational control. Chembiochem. 2007;8(8):896–902. PubMed

Galko MJ, Krasnow MA. Cellular and genetic analysis of wound healing in Drosophila larvae. PLoS Biol. 2004;2(8):E239. PubMed PMC

Antonioli L, Fornai M, Colucci R, Ghisu N, Tuccori M, et al. Pharmacological modulation of adenosine system: novel options for treatment of inflammatory bowel diseases. Inflamm Bowel Dis. 2008;14(4):566–574. PubMed

Cortés D, Guinzberg R, Villalobos-Molina R, Piña E. Evidence that endogenous inosine and adenosine-mediated hyperglycaemia during ischaemia-reperfusion through A3 adenosine receptors. Auton Autacoid Pharmacol. 2009;29(4):157–164. PubMed

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...