Lack of adenosine A3 receptors causes defects in mouse peripheral blood parameters
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
24763970
PubMed Central
PMC4152454
DOI
10.1007/s11302-014-9412-9
Knihovny.cz E-zdroje
- MeSH
- hematopoetické kmenové buňky metabolismus MeSH
- hematopoéza fyziologie MeSH
- leukocyty mononukleární metabolismus MeSH
- myši inbrední C57BL MeSH
- myši knockoutované MeSH
- myši MeSH
- receptor adenosinový A3 nedostatek MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- receptor adenosinový A3 MeSH
The role of the adenosine A3 receptor in hematopoiesis was studied using adenosine A3 receptor knockout (A3AR KO) mice. Hematological parameters of peripheral blood and femoral bone marrow of irradiated and untreated A3AR KO mice and their wild-type (WT) counterparts were investigated. Irradiation of the mice served as a defined hematopoiesis-damaging means enabling us to evaluate contingent differences in the pattern of experimentally induced hematopoietic suppression between the A3AR KO mice and WT mice. Defects were observed in the counts and/or functional parameters of blood cells in the A3AR KO mice. These defects include statistically significantly lower values of blood neutrophil and monocyte counts, as well as those of mean erythrocyte volume, mean erythrocyte hemoglobin, blood platelet counts, mean platelet volume, and plateletcrit, and can be considered to bear evidence of the lack of a positive role played by the adenosine A3 receptor in the hematopoietic system. Statistically significantly increased values of the bone marrow parameters studied in A3AR KO mice (femoral bone marrow cellularity, granulocyte/macrophage progenitor cells, and erythrocyte progenitor cells) can probably be explained by compensatory mechanisms attempting to offset the disorders in the function of blood elements in these mice. The pattern of the radiation-induced hematopoietic suppression was very similar in A3AR KO mice and their WT counterparts.
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Abbracchio MP. P1 and P2 receptors in cell growth and differentiation. Drug Dev Res. 1996;39:393–406. doi: 10.1002/(SICI)1098-2299(199611/12)39:3/4<393::AID-DDR21>3.0.CO;2-1. DOI
Neary JT, Burnstock G. Purinoceptors in the regulation of cell growth and differentiation. Drug Dev Res. 1996;39:407–412. doi: 10.1002/(SICI)1098-2299(199611/12)39:3/4<407::AID-DDR22>3.0.CO;2-X. DOI
Jacobson MA. Adenosine receptor agonists. Expert Opin Ther Patents. 2002;12:489–501. doi: 10.1517/13543776.12.4.489. DOI
Pospíšil M, Hofer M, Znojil V, Netíková J, Vácha J, Holá J, Vacek A. Granulocyte colony-stimulating factor and drugs elevating extracellular adenosine synergize to enhance haematopoietic reconstitution in irradiated mice. Eur J Haematol. 1998;60:172–180. doi: 10.1111/j.1600-0609.1998.tb01019.x. PubMed DOI
Weiterová L, Hofer M, Pospíšil M, Znojil V, Vácha J, Vacek A, Pipalová I. Influence of the joint treatment with granulocyte colony-stimulating factor and drugs elevating extracellular adenosine on erythropoietic recovery following 5-fluorouracil-induced haematotoxicity in mice. Eur J Haematol. 2000;65:310–316. doi: 10.1034/j.1600-0609.2000.065005310.x. PubMed DOI
Hofer M, Pospíšil M, Znojil V, Vacek A, Weiterová L, Holá J, Vácha J. Drugs elevating extracellular adenosine promote regeneration of haematopoietic progenitor cells in severely myelosuppressed mice: their comparison and joint effects with granulocyte colony-stimulating factor. Eur J Haematol. 2002;68:4–11. doi: 10.1034/j.1600-0609.2002.00564.x. PubMed DOI
Hofer M, Pospisil M, Weiterova L, Hoferova Z. The role of adenosine receptor agonists in regulation of hematopoiesis. Molecules. 2011;16:675–685. doi: 10.3390/molecules16010675. PubMed DOI PMC
Pospíšil M, Hofer M, Vacek A, Znojil V, Pipalová I. Effects of stable adenosine receptor agonists on bone marrow haematopoietic cells as inferred from the cytotoxic action of 5-fluorouracil. Physiol Res. 2004;54:207–213. PubMed
Hofer M, Vacek A, Pospíšil M, Holá J, Štreitová D, Znojil V. Activation of adenosine A3 receptors potentiates stimulatory effects of IL-3, SCF, and GM-CSF on mouse granulocyte-macrophage hematopoietic progenitor cells. Physiol Res. 2009;58:247–252. PubMed
Hofer M, Pospíšil M, Šefc L, Dušek L, Vacek A, Holá J, Hoferová Z, Štreitová D. Activation of adenosine A3 receptors supports hematopoiesis-stimulating effects of granulocyte colony-stimulating factor in sublethally irradiated mice. Int J Radiat Biol. 2010;86:649–656. doi: 10.3109/09553001003746075. PubMed DOI
Hofer M, Pospíšil M, Dušek L, Hoferová Z, Weiterová L. Inhibition of cyclooxygenase-2 promotes the stimulatory action of adenosine A3 receptor agonist in sublethally γ-irradiated mice. Biomed Pharmacother. 2011;65:427–431. doi: 10.1016/j.biopha.2011.04.033. PubMed DOI
Hofer M, Pospíšil M, Hoferová Z, Komůrková D, Páral P, Savvulidi F, Šefc L. The pharmacological activation of adenosine A1 and A3 receptors does not modulate the long- or short-term repopulating ability of hematopoietic stem and multipotent progenitor cells in mice. Purinerg Signal. 2013;9:207–214. doi: 10.1007/s11302-012-9340-5. PubMed DOI PMC
Wu WP, Hao JX, Halldner-Henriksson L, Xu XJ, Jacobson MA, Wiesenfeld-Hallin Z, Fredholm BB. Decreased inflammatory pain due to reduced carrageenan-induced inflammation in mice lacking adenosine A3 receptors. Neuroscience. 2002;14:523–527. doi: 10.1016/S0306-4522(02)00273-7. PubMed DOI
Fedorova IM, Jacobson MA, Basile A, Jacobson KA. Behavioral characterization of mice lacking the adenosine A3 receptor: sensitivity to hypoxic neurodegeneration. Cell Mol Neurobiol. 2003;23:431–447. doi: 10.1023/A:1023601007518. PubMed DOI PMC
Björklund O, Halldner-Henriksson L, Yang J, Eriksson TM, Jacobson MA, Fredholm BB. Decreased behavioral activation following caffeine, amphetamine and darkness in A3 adenosine receptor knock-out mice. Physiol Behav. 2008;95:668–676. doi: 10.1016/j.physbeh.2008.09.018. PubMed DOI
Hofer M, Pospíšil M, Dušek L, Hoferová Z, Weiterová L, Komůrková D. Erythropoiesis- and thrombopoiesis-characterizing parameters in adenosine A3 knock-out mice. Physiol Res. 2013;62:305–311. PubMed
Salvatore CA, Tilley ST, Latour AM, Fletcher DS, Koller BH, Jacobson MA. Disruption of the A3 adenosine receptor gene in mice and its effect on stimulated inflammatory cells. J Biol Chem. 2000;275:4429–4434. doi: 10.1074/jbc.275.6.4429. PubMed DOI
Fortin A, Harbour D, Fernandes M, Borgeat P, Bourgoin S. Differential expression of adenosine receptors in human neutrophils: up-regulation by specific Th1 cytokines and lipopolysaccharide. J Leukocyte Biol. 2006;79:574–585. doi: 10.1189/jlb.0505249. PubMed DOI
Thiele A, Kronstein R, Wetzel A, Gerth A, Nieber K, Hauschildt S. Regulation of adenosine receptor subtypes during cultivation of human monocytes: role of receptors in preventing lipopolysaccharide-triggered respiratory burst. Infect Immun. 2004;72:1349–1357. doi: 10.1128/IAI.72.3.1349-1357.2004. PubMed DOI PMC
Gessi S, Varani K, Merighi S, Cattabriga E, Avitabile A, Gavioli R, Fortini C, Leung E, Mac Lennan S, Borea PA. Expression of A3 adenosine receptors in human lymphocytes: Up-regulation in T cell activation. Mol Pharmacol. 2004;65:711–719. doi: 10.1124/mol.65.3.711. PubMed DOI
Štreitová D, Šefc L, Savvulidi F, Pospíšil M, Holá J, Hofer M. Adenosine A1, A2a, A2b, and A3 receptors in hematopoiesis. 1. Expression of receptor mRNA in four mouse hematopoietic precursor cells. Physiol Res. 2010;59:133–137. PubMed
Brugnara C, Mohandas N. Red cell indices in classification and treatment of anemia: from M. M. Wintrobe’s original 1934 classification to the third millennium. Curr Opin Hematol. 2013;20:222–230. doi: 10.1097/MOH.0b013e32835f5933. PubMed DOI