Chronic Hypoxia Enhances Adenosine Release in Rat PC12 Cells by Altering Adenosine Metabolism and Membrane Transport

Abstract: Acute exposure to hypoxia causes a release of adenosine (ADO) that is inversely related to the O2 levels in oxygen‐sensitive pheochromocytoma (PC12) cells. In the current study, chronic exposure (48 h) of PC12 cells to moderate hypoxia (5% O2) significantly enhanced the release of ADO during severe, acute hypoxia (1% O2). Investigation into the intra‐ and extracellular mechanisms underpinning the secretion of ADO in PC12 cells chronically exposed to hypoxia revealed changes in gene expression and activities of several key enzymes associated with ADO production and metabolism, as well as the down‐regulation of a nucleoside transporter. Decreases in the enzymatic activities of ADO kinase and ADO deaminase accompanied by an increase in those of cytoplasmic and ecto‐5′‐nucleotidases bring about an increased capacity to produce intra‐ and extracellular ADO. This increased potential to generate ADO and decreased capacity to metabolize ADO indicate that PC12 cells shift toward an ADO producer phenotype during hypoxia. The reduced function of the rat equilibrative nucleoside transporter rENT1 also plays a role in controlling extracellular ADO levels. The hypoxia‐induced alterations in the ADO metabolic enzymes and the rENT1 transporter seem to increase the extracellular concentration of ADO. The biological significance of this regulation is unclear but is likely to be associated with modulating cellular activity during hypoxia.

[1]  S. Kobayashi,et al.  Stimulation of Expression for the Adenosine A2A Receptor Gene by Hypoxia in PC12 Cells , 1999, The Journal of Biological Chemistry.

[2]  J. Simons,et al.  Direct comparison of GAPDH, beta-actin, cyclophilin, and 28S rRNA as internal standards for quantifying RNA levels under hypoxia. , 1999, Biochemical and biophysical research communications.

[3]  C. Culmsee,et al.  Upregulation of the Enzyme Chain Hydrolyzing Extracellular ATP after Transient Forebrain Ischemia in the Rat , 1998, The Journal of Neuroscience.

[4]  L. Conforti,et al.  Adenosine modulates hypoxia‐induced responses in rat PC12 cells via the A2A receptor , 1998, The Journal of physiology.

[5]  D. Millhorn,et al.  Hypoxia regulates the cAMP- and Ca2+/calmodulin signaling systems in PC12 cells. , 1998, Biochemical and biophysical research communications.

[6]  S. Yao,et al.  Molecular Cloning and Functional Characterization of Nitrobenzylthioinosine (NBMPR)-sensitive (es) and NBMPR-insensitive (ei) Equilibrative Nucleoside Transporter Proteins (rENT1 and rENT2) from Rat Tissues* , 1997, The Journal of Biological Chemistry.

[7]  B. Mitchell,et al.  Adenosine metabolism during phorbol myristate acetate-mediated induction of HL-60 cell differentiation: changes in expression pattern of adenosine kinase, adenosine deaminase, and 5'-nucleotidase. , 1997, Journal of immunology.

[8]  R. Simmer,et al.  Cloning and expression of the adenosine kinase gene from rat and human tissues. , 1997, Biochemical and biophysical research communications.

[9]  D. Millhorn,et al.  Regulation of tyrosine hydroxylase gene expression during hypoxia: role of Ca2+ and PKC. , 1997, Kidney international.

[10]  D. Griffith,et al.  Nucleoside and nucleobase transport systems of mammalian cells. , 1996, Biochimica et biophysica acta.

[11]  J. Geiger,et al.  Effects of iodotubercidin on adenosine kinase activity and nucleoside transport in DDT1 MF-2 smooth muscle cells. , 1996, The Journal of pharmacology and experimental therapeutics.

[12]  S. Latini,et al.  The source of brain adenosine outflow during ischemia and electrical stimulation , 1996, Neurochemistry International.

[13]  J. Geiger,et al.  Enhancement of NMDA-induced increases in levels of endogenous adenosine by adenosine deaminase and adenosine transport inhibition in rat striatum , 1995, Brain Research.

[14]  J. Geiger,et al.  Involvement of Bidirectional Adenosine Transporters in the Release of l‐[3H]Adenosine from Rat Brain Synaptosomal Preparations , 1995, Journal of neurochemistry.

[15]  B. Fredholm,et al.  Involvement of adenosine deaminase and adenosine kinase in regulating extracellular adenosine concentration in rat hippocampal slices , 1995, Neurochemistry International.

[16]  B. Fredholm Purinoceptors in the nervous system. , 1995, Pharmacology & toxicology.

[17]  A. Cook,et al.  Inhibition of adenosine kinase and adenosine uptake in guinea-pig CNS tissue by halogenated tubercidin analogues. , 1995, Life sciences.

[18]  H. Haas,et al.  Inhibition of adenosine kinase increases endogenous adenosine and depresses neuronal activity in hippocampal slices , 1994, Neuropharmacology.

[19]  T. Dunwiddie,et al.  Activity-dependent release of endogenous adenosine modulates synaptic responses in the rat hippocampus , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[20]  J. Fowler Purine release and inhibition of synaptic transmission during hypoxia and hypoglycemia in rat hippocampal slices , 1993, Neuroscience Letters.

[21]  T. White,et al.  N‐Methyl‐d‐Aspartate‐ and Non‐N‐Methyl‐d‐Aspartate‐Evoked Adenosine Release from Rat Cortical Slices: Distinct Purinergic Sources and Mechanisms of Release , 1993, Journal of neurochemistry.

[22]  H Zimmermann,et al.  5'-Nucleotidase: molecular structure and functional aspects. , 1992, The Biochemical journal.

[23]  N. Hooper,et al.  Soluble low-Km 5'-nucleotidase from electric-ray (Torpedo marmorata) electric organ and bovine cerebral cortex is derived from the glycosyl-phosphatidylinositol-anchored ectoenzyme by phospholipase C cleavage. , 1992, The Biochemical journal.

[24]  B. Fredholm,et al.  Extracellular levels of adenosine and its metabolites in the striatum of awake rats: inhibition of uptake and metabolism. , 1991, Acta physiologica Scandinavica.

[25]  J. Geiger,et al.  Improved high-pressure liquid chromatographic-fluorometric assay for measurement of adenosine in plasma. , 1991, The American journal of physiology.

[26]  Y. Misumi,et al.  Primary structure of rat liver 5'-nucleotidase deduced from the cDNA. Presence of the COOH-terminal hydrophobic domain for possible post-translational modification by glycophospholipid. , 1990, The Journal of biological chemistry.

[27]  G. A. Walter,et al.  Effects of two nucleoside transport inhibitors, dipyridamole and soluflazine, on purine release from the rat cerebral cortex , 1989, Brain Research.

[28]  A. Newby,et al.  The pigeon heart 5'-nucleotidase responsible for ischaemia-induced adenosine formation. , 1988, The Biochemical journal.

[29]  J. Deckert,et al.  Evidence for pre- and postsynaptic localization of adenosine A1 receptors in the CA1 region of rat hippocampus: a quantitative autoradiographic study , 1988, Brain Research.

[30]  A. Newby,et al.  Absolute rates of adenosine formation during ischaemia in rat and pigeon hearts. , 1988, The Biochemical journal.

[31]  P. Backlund,et al.  Amino acid sequence of S-adenosyl-L-homocysteine hydrolase from rat liver as derived from the cDNA sequence. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[32]  R. Roskoski,et al.  Activation of Tyrosine Hydroxylase in PC12 Cells by the Cyclic GMP and Cyclic AMP Second Messenger Systems , 1987, Journal of neurochemistry.

[33]  A. Newby How does dipyridamole elevate extracellular adenosine concentration? Predictions from a three-compartment model of adenosine formation and inactivation. , 1986, The Biochemical journal.

[34]  N. Tudball,et al.  Localization of S-adenosylhomocysteine hydrolase and adenosine deaminase immunoreactivities in rat brain , 1986, Brain Research.

[35]  P. Daddona,et al.  Adenosine uptake sites in rat brain: Identification using [3H]nitrobenzylthioinosine and co-localization with adenosine deaminase , 1985, Neuroscience Letters.

[36]  U. Ungerstedt,et al.  Purine levels in the intact rat brain. Studies with an implanted perfused hollow fibre , 1982, Neuroscience Letters.

[37]  R Rubio,et al.  Brain adenosine concentration during hypoxia in rats. , 1981, The American journal of physiology.

[38]  R. Perlman,et al.  Activation of tyrosine 3-monooxygenase in pheochromocytoma cells by adenosine. , 1981, The Journal of biological chemistry.

[39]  E. Newsholme,et al.  Activities and some properties of 5'-nucleotidase, adenosine kinase and adenosine deaminase in tissues from vertebrates and invertebrates in relation to the control of the concentration and the physiological role of adenosine. , 1978, The Biochemical journal.

[40]  M. M. Bradford A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. , 1976, Analytical biochemistry.

[41]  T. Dunwiddie,et al.  Role of adenosine as a modulator of synaptic activity in the central nervous system. , 1997, Advances in pharmacology.

[42]  S. Yao,et al.  Cloning of a human nucleoside transporter implicated in the Cellular uptake of adenosine and chemotherapeutic drugs , 1997, Nature Medicine.

[43]  A. Wallman-Johansson,et al.  Release of adenosine and other purines from hippocampal slices stimulated electrically or by hypoxia/hypoglycemia. Effect of chlormethiazole. , 1994, Life sciences.

[44]  B B Fredholm,et al.  Neuroprotective role of adenosine in cerebral ischaemia. , 1992, Trends in pharmacological sciences.

[45]  C. King,et al.  Measurement of adenosine, inosine and hypoxanthine in human term placenta by reversed-phase high-performance liquid chromatography. , 1986, Journal of chromatography.

[46]  B. Strehler Adenosine-5′-triphosphate and Creatine Phosphate: Determination with Luciferase , 1974 .