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Chronic Hypoxia Enhances Adenosine Release in Rat PC12 Cells by Altering Adenosine Metabolism and Membrane Transport
Author(s) -
Kobayashi Shuichi,
Zimmermann Herbert,
Millhorn David E.
Publication year - 2000
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1046/j.1471-4159.2000.740621.x
Subject(s) - adenosine , extracellular , hypoxia (environmental) , adenosine deaminase , nucleoside , nucleoside transporter , biology , transporter , metabolism , microbiology and biotechnology , adenosine kinase , biochemistry , endocrinology , chemistry , oxygen , gene , organic chemistry
Acute exposure to hypoxia causes a release of adenosine (ADO) that is inversely related to the O 2 levels in oxygen‐sensitive pheochromocytoma (PC12) cells. In the current study, chronic exposure (48 h) of PC12 cells to moderate hypoxia (5% O 2 ) significantly enhanced the release of ADO during severe, acute hypoxia (1% O 2 ). 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 rENT 1 also plays a role in controlling extracellular ADO levels. The hypoxia‐induced alterations in the ADO metabolic enzymes and the rENT 1 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.