Expression of α-and β-subunits and activity of Na+ K+ ATPase in pig thyroid cells in primary culture: Modulation by thyrotropin and thyroid hormones

Molecular and Cellular Endocrinology

Volumn 146, Issue 1-2, 1998, Pages 93-101

  Paire, A ^a   Bernier Valentin, F ^a   Rabilloud, R ^a   Watrin, C ^a   Selmi Ruby, S ^a   Rousset, B ^a  

^a UNIVERSITÉ LYON 1   (France)

Author keywords

Na+ K+ ATPase subunits; Sodium potassium adenosine triphosphatase; Thyroid cell differentiation

Indexed keywords

ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM); THYROID HORMONE; THYROTROPIN;

ANIMAL CELL; ARTICLE; CELL DIFFERENTIATION; CONTROLLED STUDY; ENZYME ACTIVITY; ENZYME REGULATION; ENZYME SUBUNIT; HORMONAL REGULATION; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; SWINE; THYROID FOLLICLE CELL;

ANIMALS; BLOTTING, WESTERN; CELL DIFFERENTIATION; CELLS, CULTURED; EPITHELIAL CELLS; GENE EXPRESSION; IODIDE PEROXIDASE; IODIDES; NA(+)-K(+)-EXCHANGING ATPASE; RNA, MESSENGER; SWINE; THYROGLOBULIN; THYROID GLAND; THYROID HORMONES; THYROTROPIN;

EID: 0032567144     PISSN: 03037207     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0303-7207(98)00192-0     Document Type: Article

References (41)

1. +-ATPase α1 gene expression through the interaction of aldosterone and cAMP-inducible transcriptional factors. Steroids. 60:1995;147-152.
2. Akiguchi I., Strauss K., Borges M., Silva J.E., Moses A.C. Thyroid hormone receptors and 3,5,3′-triiodothyronine biological effects in FRTL5 thyroid follicular cells. Endocrinology. 131:1992;1279-1287.
3. +-ATPase is an effector protein for protein kinase C in renal proximal tubule cells. Am. J. Physiol. 256:1989;F370-F373.
4. Bourke J.R., Matainaho T., Huxham G.J., Manley S.W. Cyclic AMP-stimulated fluid transport in the thyroid: influence of thyroid stimulators, amiloride and acetazolamide on the dynamics of domes in monolayer cultures of porcine thyroid cells. J. Endocrinol. 115:1987;19-26.
5. Carrasco N. Iodide transport in the thyroid gland. Biochim. Biophys. Acta. 1154:1993;65-82.
6. Chomczynski P., Sacchi N. Single step method of RNA isolation by acid guanidium thiocyanate phenol chloroform extraction. Anal. Biochem. 162:1987;156-159.
7. Dai G., Levy O., Carrasco N. Cloning and characterization of the thyroid iodide transporter. Nature. 379:1996;458-460.
8. Desai-Yajnik V., Zeng J., Omori K., Sherman J., Morimoto T. The effect of thyroid hormone treatment on the gene expression and enzyme activity of rat liver sodium-potassium dependent adenosine triphosphatase. Endocrinology. 136:1995;629-639.
9. Dumont J.E. The action of thyrotropin on thyroid metabolism. Vitam. Horm. 29:1971;287-412.
10. Dumont J.E., Lamy F., Roger P., Maenhaut C. Physiological and pathological regulation of thyroid cell proliferation and differentiation by thyrotropin and other factors. Physiol. Rev. 72:1992;667-697.
11. Fayet G., Michel-Béchet M., Lissitzky S. Thyrotropin-induced aggregation and reorganization into follicles of isolated porcine thyroid cells 2: ultrastructural studies. Eur. J. Biochem. 24:1971;100-111.
12. Feng J., Orlowski J., Lingrel B. Identification of a functional thyroid response element in the upstream flanking region of the human Na, K-ATPase β1 gene. Nucleic Acids Res. 21:1993;2619-2626.
13. Fiske C.R., Subbarow Y. The colorimetric determination of phosphorus. J. Biol. Chem. 66:1925;375-400.
14. Geering K. Subunit assembly and functional maturation of Na,K-ATPase. J. Membr. Biol. 115:1990;109-121.
15. Gick G.G., Ismail-Beigi F., Edelman I.S. Thyroidal regulation of rat renal and hepatic Na,K-ATPase gene expression. J. Biol. Chem. 263:1988;16610-16618.
16. +-ATPase from intracellular compartments to the plasma membrane in mammalian skeletal muscle. J. Biol. Chem. 267:1992;5040-5043.
17. Horisberger J.D., Lemas V., Kraehenbühl J.P, Rossier B.C. Structure-function relationship of Na,K-ATPase. Ann. Rev. Physiol. 53:1991;565-584.
18. Ismail-Beigi F. Thyroid hormone regulation of Na,K-ATPase expression. Trends Endocrinol. Metab. 4:1993;152-155.
19. +)-ATPase III: purification from the outer medulla of mammalian kidney after selective removal of membrane components by sodium dodecylsulfate. Biochim. Biophys. Acta. 223:1974;36-52.
20. +)-ATPase. Biochim. Biophys. Acta. 694:1982;27-68.
21. Kogai T., Endo T., Saito T., Miyazaki A., Kawaguchi A., Onaya T. Regulation by thyroid-stimulating hormone of sodium/iodide symporter gene expression and protein levels in FRTL-5 cells. Endocrinology. 138:1997;2227-2232.
22. - symporter with an anti-COOH terminus antibody. Proc. Natl. Acad. Sci. USA. 94:1997;5568-5573.
23. Lingrel J.B. Na,K-ATPase: Isoform structure, function, and expression. J. Bioenerg. Biomembr. 24:1992;263-270.
24. +-ATPase. J. Biol. Chem. 269:1994;19659-19662.
25. Lissitzky S., Fayet G., Giraud A., Verrier B., Torresani J. Thyrotropin-induced aggregation and reorganization into follicles of isolated porcine thyroid cells 1: mechanism of action of thyrotropin and metabolic properties. Eur. J. Biochem. 24:1971;88-99.
26. +-ATPase β1 subunit gene. Biochim. Biophys. Acta. 1130:1992;336-338.
27. Magnusson R.P., Gestautas J., Seto P., Taurog A., Rapoport B. Isolation and characterization of a cDNA clone for porcine thyroid peroxidase. FEBS Lett. 208:1986;391-396.
28. Malthièry Y., Lissitzky S. Primary structure of human thyroglobulin deduced from the sequence of its 8448 base complementary DNA. Eur. J. Biochem. 165:1987;491-498.
29. Mauchamp J., Margotat A., Chambard M., Charrier B., Remy L., Michel-Béchet M. Polarity of three-dimensional structures derived from isolated hog thyroid cells in primary culture. Cell. Tissue Res. 204:1979;417-430.
30. +)ATPase. J. Biol. Chem. 266:1991;15824-15831.
31. Munari-Silem Y., Mesnil M., Selmi S., Bernier-Valentin F., Rabilloud R., Rousset B. Cell-cell interactions in the process of differentiation of thyroid epithelial cells into follicles: a study by microinjection and fluorescence microscopy on in vitro reconstituted thyroid follicles. J. Cell. Physiol. 145:1990;414-427.
32. Paire A., Bernier-Valentin F., Selmi-Ruby S., Rousset B. Characterization of the rat thyroid iodide transporter using anti-peptide antibodies. J. Biol. Chem. 272:1997;18245-18249.
33. +-ATPase in cultured thyroid follicular cells. Am. J. Physiol. 268:1995;C1252-C1258.
34. Rossier B.C., Geering K., Kraehenbuhl J.P. Regulation of the sodium pump: how and why? Trends Biochem. Sci. 12:1987;483-487.
35. Rousset B., Poncet C., Mornex R. Evidence for a secretion of thyroxine by isolated hog thyroid cells. Biochim. Biophys. Acta. 437:1976;543-561.
36. Selmi-Ruby S., Rousset B. Analysis of the functional state of T3 nuclear receptors expressed in thyroid cells. Mol. Cell. Endocrinol. 119:1992;95-104.
37. Shull G.E., Pugh D.G., Lingrel J.B. The human Na,K-ATPase alpha 1 gene: characterization of the 5′-flanking region and identification of a restriction fragment length polymorphism. Genomics. 6:1990;451-460.
38. - symporter mRNAs in dog thyroid. Mol. Cell. Endocrinol. 131:1997;195-203.
39. Wolff J. Transport of iodide and other anions in the thyroid gland. Physiol. Rev. 44:1964;45-90.
40. Yagawa Y., Kawakami K., Nagano K. Cloning and analysis of the 5′ flanking region of the rat Na,K-ATPase α1-subunit gene. Biochim. Biophys. Acta. 1049:1990;286-292.
41. +-ATPase β subunit protein. J. Biol. Chem. 262:1987;4905-4910.