Induction of mRNAs and proteins for Na/K ATPase α1 and β1 subunits following hypoxia/reoxygenation in astrocytes

Molecular Brain Research

Volumn 110, Issue 1, 2003, Pages 38-44

  Kasai, Kosuke ^a,b   Yamashita, Toshihide ^a,b   Yamaguchi, Atsushi ^a,b   Yoshiya, Kazuhisa ^a,b   Kawakita, Akihiro ^a,b   Tanaka, Hiroshi ^a   Sugimoto, Hisashi ^a   Tohyama, Masaya ^a,b  

^a OSAKA UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^b JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

Author keywords

Astrocytes; Hypoxia; Na K ATPase; Reoxygenation

Indexed keywords

ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM); MESSENGER RNA;

ARTICLE; ASTROCYTE; CELL SURVIVAL; DNA ISOLATION; DNA LIBRARY; GENE EXPRESSION; HYPOXIA; PRIORITY JOURNAL; PROTEIN INDUCTION; REOXYGENATION;

ANIMALS; ASTROCYTES; CELL HYPOXIA; CELL SURVIVAL; CELLS, CULTURED; GENE EXPRESSION REGULATION, ENZYMOLOGIC; NA(+)-K(+)-EXCHANGING ATPASE; OXYGEN; RATS; RATS, SPRAGUE-DAWLEY; REPERFUSION INJURY; RNA, MESSENGER;

EID: 0037474170     PISSN: 0169328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0169-328X(02)00581-8     Document Type: Article

References (37)

1. +-ATPase activity after hypoxia and reoxygenation in the perfused rat liver: an electron microscopic cytochemical study. J. Hepatol. 22:1995;565-575.
2. Arthur F.E., Shivers R.R., Bowman P.D. Astrocyte-mediated induction of tight junctions in brain capillary endothelium: an efficient in vitro model. Brain Res. 433:1987;155-159.
3. +) ATPase after in vitro hypoxia and reoxygenation are affected by methods of membrane preparation. J. Neurosci. Methods. 79:1998;201-206.
4. Boldyrev A.A., Bulygina E.R. Na/K ATPase and oxidative Stress. Ann. N Y Acad. Sci. 834:1997;666-668.
5. Boldyrev A.A., Kurella E. Mechanism of oxidative damage of kidney Na/K ATPase. Biophys. Res. Commun. 222:1996;483-487.
6. Chow D.C., Forte J.G. Functional significance of the β-subunit for heterodimeric P-type ATPases. J. Exp. Biol. 198:1995;1-17.
7. Clerici C., Matthay M.A. Hypoxia regulates gene expression of alveolar epithelial transport proteins. J. Appl. Physiol. 88:2000;1890-1896.
8. Dobrota D., Matejovicova M., Kurella E.G., Boldyrev A.A. Na/K-ATPase under oxidative stress: molecular mechanisms of injury. Cell. Mol. Neurobiol. 19:1999;141-149.
9. +-ATPase β1 subunit gene improves alveolar fluid human. Gene Therapy. 11:2000;2231-2242.
10. Feinberg A.P., Vogelstein B. A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. Anal. Biochem. 132:1983;6-13.
11. Geering K. Subunit assembly and functional maturation of Na,K-ATPase. J. Membr. Biol. 115:1990;109-121.
12. Golden W.C., Brambrink A.M., Traystman R.J., Martin L.J. Failure to sustain recovery of Na, K-ATPase function is a possible mechanism for striatal neurodegeneration in hypoxic-ischemic newborn piglets. Mol. Brain Res. 88:2001;94-102.
13. Henn F.A., Haljamae H., Hamberger A. Glial cell function: active control of extracellular K+ concentration. Brain Res. 43:1972;437-443.
14. Hochachka P.W., Buck L.T., Doll C.J., Land S.C. Unifying theory of hypoxia tolerance: molecular/metabolic defence and mechanisms for surviving oxygen lack. Proc. Natl. Acad. Sci. 93:1996;9493-9498.
15. Hori O., Matsumoto M., Kuwabara K., Maeda Y., Ueda H., Ohtsuki T., Kinoshita T., Ogawa S., Stern D.M., Kamada T. Exposure of astrocytes to hypoxia/reoxygenation enhances expression of glucose-regulated protein 78 facilitating astrocyte release of the neuroprotective cytokine interleukin 6. J. Neurochem. 66:1996;973-979.
16. Hori O., Matsumoto M., Maeda Y., Ueda H., Ohtsuki T., Stern D.M., Kinoshita T., Ogawa S., Kamada T. Metabolic and biosynthetic alterations in cultured astrocytes exposed to hypoxia/reoxygenation. J. Neurochem. 62:1994;1489-1495.
17. Karakurum M., Shreeniwas R., Chen J., Pinsky D., Yan S.D., Anderson M., Sunouchi K., Major J., Hamilton T., Kuwabara K. Hypoxic induction of interleukin-8 gene expression in human endothelial cells. J. Clin. Invest. 93:1994;1564-1570.
18. Kochanek P.M. Ischemic and traumatic brain injury: pathobiology and cellular mechanisms. Crit. Care Med. 21:(9 Suppl.):1993;S333-S335.
19. Koga S., Ogawa S., Kuwabara K., Brett J., Leavy J.A., Ryan J., Koga Y., Plocinski J., Benjamin W., Burns D.K. Synthesis and release of interleukin 1 by reoxygenated human mononuclear phagocytes. J. Clin. Invest. 90:1992;1007-1015.
20. Kuwabara K., Matsumoto M., Ikeda J., Hori O., Ogawa S., Maeda Y., Kitagawa K., Imuta N., Kinoshita T., Stern D.M., Yanagi H., Kamada T. Purification and characterization of a novel stress protein, the 150-kDa oxygen-regulated protein (ORP150), from cultured rat astrocytes and its expression in ischemic mouse brain. J. Biol. Chem. 271:1996;5025-5032.
21. Liang P., Pardee A.B. Differential display of eukaryotic messenger RNA by means of the polymerase chain reaction. Science. 257:1992;967-971.
22. Loike J.D., Cao L., Brett J., Ogawa S., Silverstein S.C., Stern D. Hypoxia induces glucose transporter expression in endothelial cells. Am. J. Physiol. 263:1992;C326-333.
23. Maeda Y., Matsumoto M., Hori O., Kuwabara K., Ogawa S., Yan S.D., Ohtsuki T., Kinoshita T., Kamada T., Stern D.M. Hypoxia/reoxygenation-mediated induction of astrocyte interleukin 6: a paracrine mechanism potentially enhancing neuron survival. J. Exp. Med. 180:1994;2297-2308.
24. Marrif H., Bernhard H., Juurlink J. Astrocytes respond to hypoxia by increasing glycolytic capacity. J. Neurosci. Res. 57:1999;255-260.
25. Matsuo N., Ogawa S., Imai Y., Takagi T., Tohyama M., Stern D., Wanaka A. Cloning of a novel RNA binding polypeptide (RA301) induced by hypoxia/reoxygenation. J. Biol. Chem. 270:1995;28216-28222.
26. Magistretti P.J., Manthorpe M., Bloom F.E., Varon S. Functional receptors for vasoactive intestinal polypeptide in cultured astroglia from neonatal rat brain. Regul. Pept. 6:1983;71-80.
27. Maulik D., Qayyum I., Powell S.R., Karantza M., Mishra O.P., Delivoria-Papadopoulos M. Post-hypoxic magnesium decreases nuclear oxidative damage in the fetal guinea pig brain. Brain Res. 890:2001;130-136.
28. McCord J.M. Oxygen-derived free radicals in postischemic tissue injury. N. Engl. J. Med. 312:1985;159-163.
29. Ogawa S., Gerlach H., Esposito C., Pasagian-Macaulay A., Brett J., Stern D. Hypoxia modulates the barrier and coagulant function of cultured bovine endothelium. Increased monolayer permeability and induction of procoagulant properties. J. Clin. Invest. 85:1990;1090-1098.
30. +-ATPase. Membr. Cell Biol. 13:2000;745-788.
31. Ross S.T., Soltesz I. Selective depolarization of interneurons in the early posttraumatic dentate gyrus: involvement of the Na(+)/K(+)-ATPase. J. Neurophysiol. 83:2000;2916-2930.
32. Schousboe A., Svenneby G., Hertz L. Uptake and metabolism of glutamate in astrocytes cultured from dissociated mouse brain hemispheres. J. Neurochem. 29:1977;999-1005.
33. Stanimirovic D.B., Ball R., Durkin J.P. Stimulation of glutamate uptake and Na,K-ATPase activity in rat astrocytes exposed to ischemia-like insults. Glia. 19:1997;123-134.
34. Swanson A.R., Choi D.W. Glial glycogen stores affect neuronal survival during glucose deprivation in vitro. J. Cereb. Blood Flow Metab. 13:1993;162-169.
35. Takahashi S., Shibata M., Gotoh J., Fukuuchi Y. Astroglial cell death induced by excessive influx of sodium ions. Eur. J. Pharmacol. 408:2000;127-135.
36. Wilson R.E., Sutherland R.M. Enhanced synthesis of specific proteins, RNA, and DNA caused by hypoxia and reoxygenation. Int. J. Radiat. Oncol. Biol. Phys. 16:1989;957-961.
37. Wissemann H., Anundi D., Lauchart W., Viebahn R., de Groot H. Differences in glycolytic capacity and hypoxia tolerance between hepatoma cells and hepatocytes. Hepatology. 13:1991;297-303.