Literature DB >> 1645712

Dexamethasone markedly induces Na,K-ATPase mRNA beta 1 in a rat liver cell line.

A Bhutada1, W W Wassynger, F Ismail-Beigi.   

Abstract

Exposure of Clone 9 cells, a "nontransformed" rat liver cell line, to 10(-8) M dexamethasone resulted at 3 h in 1.8 +/- 0.2- and 40 +/- 5-fold increases in mRNA alpha 1 and mRNA beta 1 content, respectively, an effect that was not mimicked by 10(-8) M aldosterone. The increments in mRNA alpha 1 and mRNA beta 1 abundances in total cell RNA were half-maximal at 5 x 10(-9) M dexamethasone and persisted for more than 24 h. Na,K-ATPase activity, however, increased only slightly (by 9%) at 24 h. The induction of mRNA beta 1 by dexamethasone was not prevented by the presence of cycloheximide. mRNA beta 1 abundance increased earlier in the nuclear RNA pool (becoming apparent within 45 min) than in the cytoplasmic RNA pool, consistent with a precursor-product relationship. Moreover, putative pre-mRNA beta 1 bands of approximately 4,600 and approximately 12,000 nucleotides accumulated in the nRNA pool after 1 h of exposure to dexamethasone. Incubation in the presence of dexamethasone for 3 h enhanced the incorporation of [3H]uridine into total cell mRNA alpha 1 and mRNA beta 1 by 1.3- and 12-fold, respectively. In nuclear run-on assays, however, transcription of mRNA alpha 1 and mRNA beta 1 was not altered after 30 min of exposure to 10(-8) M dexamethasone. The abundance of mRNA beta 1 in rat liver also increased markedly (greater than 30-fold) in rats treated with the hormone for 6 h. We conclude that dexamethasone causes an induction of Na,K-ATPase subunit mRNAs, an effect that is markedly greater for mRNA beta 1 than for mRNA alpha 1. The increases in subunit mRNA content, however, are associated with, at most, a small increase in Na,K-ATPase activity, suggesting that the increments in mRNA abundances, especially that of mRNA beta 1, do not play a determining role in the regulation of Na,K-ATPase activity in these cells.

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Year:  1991        PMID: 1645712

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  7 in total

1.  Role of enhanced Na+ entry in the control of Na,K-ATPase gene expression by serum.

Authors:  A Kirtane; N Ismail-Beigi; F Ismail-Beigi
Journal:  J Membr Biol       Date:  1994-01       Impact factor: 1.843

2.  Regulation of Na+,K(+)-ATPase and the Na+/K+/Cl- co-transporter in the renal epithelial cell line NBL-1 under osmotic stress.

Authors:  A Ferrer-Martinez; F J Casado; A Felipe; M Pastor-Anglada
Journal:  Biochem J       Date:  1996-10-15       Impact factor: 3.857

3.  Aldosterone and thyroid hormone modulation of alpha 1-, beta 1-mRNA, and Na,K-pump sites in rabbit distal colon epithelium. Evidence for a novel mechanism of escape from the effect of hyperaldosteronemia.

Authors:  H Wiener; J M Nielsen; D A Klaerke; P L Jørgensen
Journal:  J Membr Biol       Date:  1993-05       Impact factor: 1.843

4.  Regulation of rat renal (Na(+) + K+)-adenosine triphosphatase mRNA levels by corticosterone.

Authors:  L E Klein; C S Lo
Journal:  Experientia       Date:  1992-08-15

5.  Cellular responses to steroids in the enhancement of Na+ transport by rat collecting duct cells in culture. Differences between glucocorticoid and mineralocorticoid hormones.

Authors:  J R Laplace; R F Husted; J B Stokes
Journal:  J Clin Invest       Date:  1992-10       Impact factor: 14.808

6.  Induction of GLUT1 mRNA in response to azide and inhibition of protein synthesis.

Authors:  A Behrooz; F Ismail-Beigi
Journal:  Mol Cell Biochem       Date:  1998-10       Impact factor: 3.396

Review 7.  Transcriptional regulators of Na,K-ATPase subunits.

Authors:  Zhiqin Li; Sigrid A Langhans
Journal:  Front Cell Dev Biol       Date:  2015-10-26
  7 in total

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