Distribution of Na,K-ATPase is normal in the inner ear of a mouse with a null mutation of the glucocorticoid receptor

Hearing Research

Volumn 124, Issue 1-2, 1998, Pages 146-154

  Erichsen, Susan ^a   Stierna, Pontus ^a   Bagger Sjöbäck, Dan ^a   Curtis, Lisa M ^b   Rarey, Kyle E ^b   Schmid, Wolfgang ^c   Hultcrantz, Malou ^a  

^a KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

^b UNIVERSITY OF FLORIDA   (United States)

^c GERMAN CANCER RESEARCH CENTER DKFZ   (Germany)

Author keywords

Glucocorticoid receptor; Homologous recombination; Immunohistochemistry; Inner ear; Mouse; Na,K ATPase

Indexed keywords

ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM); GLUCOCORTICOID RECEPTOR; MESSENGER RNA;

ANIMAL CELL; ARTICLE; EMBRYO; ENZYME LOCALIZATION; ENZYME SUBUNIT; GENE MUTATION; GENETIC RECOMBINATION; HEARING; HORMONAL REGULATION; IMMUNOHISTOCHEMISTRY; INNER EAR; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROPRIOCEPTION;

EID: 0031761615     PISSN: 03785955     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-5955(98)00117-8     Document Type: Article

References (28)

1. Anniko M., Wróblewski R. Ionic environment of cochlear hair cells. Hear. Res. 22:1986;279-293.
2. Cole T.J., Blendy J.A., Monaghan P.A., Schmid W., Aguzzi A., Schutz G. Molecular genetic analysis of glucocorticoid signalling during mouse development. Steroids. 60:1995;93-96.
3. Curtis L.M., ten Cate W.-J.F., Rarey K.E. Dynamics of Na,K-ATPase sites in the lateral cochlear wall tissues of the rat. Eur. Arch. Otorhinolaryngol. 250:1993;265-270.
4. + exchange isoforms: physiological and pathophysiological relevance. J. Cardiovasc. Pharmacol. 22:1993;96-98.
5. Erichsen S., Bagger-Sjöbäck D., Curtis L., Zuo J., Rarey K., Hultcrantz M. Appearance of glucocorticoid receptors in the inner ear of the mouse during development. Acta Otolaryngol. (Stockh.). 116:1996;721-725.
6. Erichsen S., Zuo J., Curtis L., Rarey K., Hultcrantz M. Na,K-ATPase α- and β-isoforms in the developing inner ear of the mouse. Hear. Res. 100:1996;143-149.
7. Furuta H., Mori N., Sato C., Hoshikawa H., Sakai S., Iwakura S., Doi K. Mineralocorticoid type I receptor in the rat cochlea: mRNA identification by polymerase chain reaction (PCR) and in situ hybridisation. Hear. Res. 78:1994;175-180.
8. Horner K.C. Old theme and new reflections: hearing impairment associated with endolymphatic hydrops. Hear. Res. 52:1991;147-156.
9. Lim D.J., Anniko M. Developmental morphology of the mouse inner ear. Acta Otolaryngol. (Stockh.). 422:1985;5-22.
10. Lingrel J.B. Na,K-ATPase: isoform structure, function, and expression. J. Bioenerg. Biomembr. 24:1992;263-270.
11. Lohuis P.J.F.M., ten Cate W.-J.F., Patterson K.E., Rarey K.E. Modulation of the rat stria vascularis in the absence of circulating adrenocorticosteroids. Acta Otolaryngol. (Stockh.). 110:1990;348-356.
12. Luttge W.G., Davda M.M., Rupp M.E., Kang C.G. High affinity binding and regulatory actions of dexamethasone-type I receptor complexes in mouse brain. Endocrinology. 125:1989;1194-1203.
13. Mikaelian D., Ruben R.J. Development of hearing in the normal CBA-J mouse. Acta Otolaryngol. (Stockh.). 59:1964;451-461.
14. Mujais S.K., Chekal M.A., Jones W.J., Hayslett J.P., Katz A.I. Modulation of renal sodium-potassium-adenosine triphosphate by aldosterone. Effect of high physiologic levels on enzyme activity in isolated rat and rabbit tubules. J. Clin. Invest. 76:1989;170-176.
15. Offner F.F., Dallos P., Cheatham M.A. Positive endocochlear potential: Mechanisms of production by marginal cells of stria vascularis. Hear. Res. 29:1987;117-124.
16. Orlowski J., Lingrel J.B. Tissue-specific and developmental regulation of the rat Na,K-ATPase catalytic α isoform and β subunit mRNAs. J. Biol. Chem. 263:1988;10436-10442.
17. Paparella M.M. Pathogenesis and pathophysiology of Ménière's disease. Acta Otolaryngol. (Stockh.). 485:1991;26-35.
18. Rarey K.E., Luttge W.G. Presence of type I and type II/IB receptors for adrenocorticosteroid hormones in the inner ear. Hear. Res. 41:1989;217-222.
19. Rarey K.E., Tyneway D., Patterson K. Decreased adenosine triphosphatase activity in the absence of adrenocorticosteroids. Arch. Otolaryngol. Head Neck Surg. 115:1989;817-821.
20. Rarey K.E., Curtis L.M., ten Cate W.-J.F. Tissue specific levels of glucocorticoid receptor within the rat inner ear. Hear. Res. 64:1993;205-210.
21. Rarey K.E., Gerhardt K.J., Curtis L.M., ten Cate W.J.F. Effect of stress on cochlear glucocorticoid protein: Acoustic stress. Hear. Res. 82:1995;135-138.
22. Rose A.M., Valdes R. Understanding the sodium pump and its relevance to disease. Clin. Chem. 40:1994;1674-1685.
23. Salt A.N., Melichar I., Thalmann R. Mechanisms of endocochlear potential generation by stria vascularis. Laryngoscope. 97:1987;984-991.
24. Schmid W., Cole T.J., Blendy J.A., Schuetz G. Molecular genetic analysis of glucocorticoid signalling in development. J. Steroid Mol. Biol. 53:1995;33-35.
25. ten Cate W.-J.F., Curtis L.M., Small G.M., Rarey K.E. Localization of glucocorticoid receptors and glucocorticoid receptor mRNAs in the rat cochlea. Laryngoscope. 103:1993;865-871.
26. 2+-ATPase activity in the lateral wall of the guinea pig. Arch. Otorhinolaryngol. 243:1987;395-400.
27. Zuo J., Curtis L., Yao X., Bagger-Sjöbäck D., Hultcrantz M., Rarey K. Glucocorticoid receptor expression in the postnatal rat cochlea. Hear. Res. 87:1995;220-227.
28. Zuo J., Curtis L., Yao X., ten Cate W.-J.F., Rarey K. Expression of Na,K-ATPase α and β isoforms in the neonatal rat cochlea. Acta Otolaryngol. (Stockh.). 115:1995;497-503.