A Role for Adenosine Deaminase in Drosophila Larval Development

Adenosine deaminase (ADA) is an enzyme present in all organisms that catalyzes the irreversible deamination of adenosine and deoxyadenosine to inosine and deoxyinosine. Both adenosine and deoxyadenosine are biologically active purines that can have a deep impact on cellular physiology; notably, ADA deficiency in humans causes severe combined immunodeficiency. We have established a Drosophila model to study the effects of altered adenosine levels in vivo by genetic elimination of adenosine deaminase-related growth factor-A (ADGF-A), which has ADA activity and is expressed in the gut and hematopoietic organ. Here we show that the hemocytes (blood cells) are the main regulator of adenosine in the Drosophila larva, as was speculated previously for mammals. The elevated level of adenosine in the hemolymph due to lack of ADGF-A leads to apparently inconsistent phenotypic effects: precocious metamorphic changes including differentiation of macrophage-like cells and fat body disintegration on one hand, and delay of development with block of pupariation on the other. The block of pupariation appears to involve signaling through the adenosine receptor (AdoR), but fat body disintegration, which is promoted by action of the hemocytes, seems to be independent of the AdoR. The existence of such an independent mechanism has also been suggested in mammals.

[1]  M. Hershfield New insights into adenosine‐receptor‐mediated immunosuppression and the role of adenosine in causing the immunodeficiency associated with adenosine deaminase deficiency , 2005, European journal of immunology.

[2]  V. Henrich,et al.  Cell-autonomous roles of the ecdysoneless gene in Drosophila development and oogenesis , 2004, Development.

[3]  J. Truman,et al.  Overexpression of broad: a new insight into its role in the Drosophila prothoracic gland cells , 2004, Journal of Experimental Biology.

[4]  R. Rizki,et al.  A mutant affecting the crystal cells inDrosophila melanogaster , 1980, Wilhelm Roux's archives of developmental biology.

[5]  A. Goto,et al.  Drosophila hemolectin gene is expressed in embryonic and larval hemocytes and its knock down causes bleeding defects. , 2003, Developmental biology.

[6]  R. Klapper,et al.  The two origins of hemocytes in Drosophila , 2003, Development.

[7]  P. Bryant,et al.  Genetic analysis of the ADGF multigene family by homologous recombination and gene conversion in Drosophila. , 2003, Genetics.

[8]  I. Zhimulev,et al.  EcR isoforms in Drosophila: testing tissue-specific requirements by targeted blockade and rescue , 2003, Development.

[9]  I. Andó,et al.  Analysis of Ras-induced overproliferation in Drosophila hemocytes. , 2003, Genetics.

[10]  K. Beckingham,et al.  The Dorothy enhancer has tinman binding sites and drives hopscotch‐induced tumor formation , 2002, Genesis.

[11]  E. Vizi,et al.  Adenosine: a potential mediator of immunosuppression in multiple organ failure. , 2002, Current opinion in pharmacology.

[12]  S. Alam,et al.  Clustered Charged Amino Acids of Human Adenosine Deaminase Comprise a Functional Epitope for Binding the Adenosine Deaminase Complexing Protein CD26/Dipeptidyl Peptidase IV* , 2002, The Journal of Biological Chemistry.

[13]  Xiaofeng Zhou,et al.  Broad specifies pupal development and mediates the 'status quo' action of juvenile hormone on the pupal-adult transformation in Drosophila and Manduca. , 2002, Development.

[14]  P. Bryant,et al.  Adenosine deaminase-related growth factors stimulate cell proliferation in Drosophila by depleting extracellular adenosine , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[15]  J. Hoffmann,et al.  Drosophila innate immunity: an evolutionary perspective , 2002, Nature Immunology.

[16]  S. Graham,et al.  Characterization of the adenosine deaminase-related growth factor (ADGF) gene family in Drosophila. , 2001, Gene.

[17]  S. Latini,et al.  Adenosine in the central nervous system: release mechanisms and extracellular concentrations , 2001, Journal of neurochemistry.

[18]  G. Nagle,et al.  Mollusk-derived growth factor: cloning and developmental expression in the central nervous system and reproductive tract of Aplysia. , 2001, Brain research. Molecular brain research.

[19]  Y. Lu,et al.  Glue secretion in the Drosophila salivary gland: a model for steroid-regulated exocytosis. , 2001, Developmental biology.

[20]  R. Lanot,et al.  Postembryonic hematopoiesis in Drosophila. , 2001, Developmental biology.

[21]  S. Natori,et al.  Male-specific IDGF, a Novel Gene Encoding a Membrane-bound Extracellular Signaling Molecule Expressed Exclusively in Testis of Drosophila melanogaster * , 2000, The Journal of Biological Chemistry.

[22]  B. Sperlágh,et al.  Ischemic-like condition releases norepinephrine and purines from different sources in superfused rat spleen strips , 2000, Journal of Neuroimmunology.

[23]  S. Natori,et al.  A novel hemocyte-specific membrane protein of Sarcophaga (flesh fly). , 2000, European journal of biochemistry.

[24]  James J. Lee,et al.  Metabolic Consequences of Adenosine Deaminase Deficiency in Mice Are Associated with Defects in Alveogenesis, Pulmonary Inflammation, and Airway Obstruction , 2000, The Journal of experimental medicine.

[25]  S. Aksoy,et al.  A family of genes with growth factor and adenosine deaminase similarity are preferentially expressed in the salivary glands of Glossina m. morsitans. , 2000, Gene.

[26]  M. Sitkovsky,et al.  A2A receptor dependent and A2A receptor independent effects of extracellular adenosine on murine thymocytes in conditions of adenosine deaminase deficiency , 2000 .

[27]  M. Aldrich,et al.  The importance of adenosine deaminase for lymphocyte development and function. , 2000, Biochemical and biophysical research communications.

[28]  J. Ribeiro,et al.  The salivary adenosine deaminase from the sand fly Lutzomyia longipalpis. , 2000, Experimental parasitology.

[29]  B. Roe,et al.  The human homolog of insect-derived growth factor, CECR1, is a candidate gene for features of cat eye syndrome. , 2000, Genomics.

[30]  J. F. Chen,et al.  A(2A) receptor dependent and A(2A) receptor independent effects of extracellular adenosine on murine thymocytes in conditions of adenosine deaminase deficiency. , 2000, Blood.

[31]  P. Heitzler,et al.  Requirement for croquemort in phagocytosis of apoptotic cells in Drosophila. , 1999, Science.

[32]  G. Burnstock,et al.  Increased release of ATP from endothelial cells during acute inflammation , 1998, Inflammation Research.

[33]  S. Govind,et al.  A role for the Drosophila Toll/Cactus pathway in larval hematopoiesis. , 1998, Development.

[34]  J. Puck,et al.  Human severe combined immunodeficiency: genetic, phenotypic, and functional diversity in one hundred eight infants. , 1997, The Journal of pediatrics.

[35]  S. Natori,et al.  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)* , 1996, The Journal of Biological Chemistry.

[36]  R. Schulz,et al.  Wingless signaling induces nautilus expression in the ventral mesoderm of the Drosophila embryo. , 1996, Developmental biology.

[37]  T. Yano,et al.  Regulation of the expression of cathepsin B in Sarcophaga peregrina (flesh fly) at the translational level during metamorphosis. , 1995, European journal of biochemistry.

[38]  N. Perrimon,et al.  Targeted gene expression as a means of altering cell fates and generating dominant phenotypes. , 1993, Development.

[39]  S. Kurata,et al.  The 29-kDa hemocyte proteinase dissociates fat body at metamorphosis of Sarcophaga. , 1992, Developmental biology.

[40]  L. Gilbert,et al.  Metamorphosis of the corpus allatum and degeneration of the prothoracic glands during the larval-pupal-adult transformation of Drosophila melanogaster: a cytophysiological analysis of the ring gland. , 1991, Developmental biology.

[41]  B. Cowan,et al.  A Family Is , 1981 .

[42]  L. Kauvar,et al.  Roles of ecdysone in Drosophila development. , 1977, Proceedings of the National Academy of Sciences of the United States of America.

[43]  M. Rizki Tumor formationin relation to metamorphosis in Drosophila melanogaster , 1957 .

[44]  J. C. Li,et al.  Development in DROSOPHILA MELANOGASTER. , 1927, Genetics.