Literature DB >> 2521337

Retinoic acid is a modulator of thyroid hormone activation of Ca2+-ATPase in the human erythrocyte membrane.

T J Smith1, F B Davis, P J Davis.   

Abstract

The thyroid hormones thyroxine (T4) and 3,3',5-L-triiodothyronine (T3) stimulate plasma membrane Ca2+-ATPase (EC 3.6.1.3) activity in human erythrocytes by a mechanism independent of the cell nucleus. The current studies were conducted to determine the effect of retinoic acid on the extranuclear activation by T4 and T3 of Ca2+-ATPase in the human red cell. The retinoid inhibited basal and T4-stimulatable activity of that enzyme in a dose-dependent manner. At the highest tested concentration (10(-6) M), retinoic acid inhibited basal enzyme activity by 25% and T4-stimulated activity by 72%. A concentration as low as 5 x 10(-10) M retinoic acid shifted the dose-response curve of both T4 and T3 so that the concentration of each associated with maximal enzyme stimulation was 10(-9) M instead of 10(-10) M. Retinoic acid displaced [125I]T4 binding to red cell membranes as effectively as unlabeled T4. Retinol failed to influence either basal or T4-stimulated enzyme activity or to displace T4 binding. These results indicate that retinoic acid can partially block the T4 and T3 stimulation of Ca2+-ATPase in human red cell membranes and suggest a physiologic role for the retinoid as a modulator of this peripheral action of thyroid hormone. They suggest that the red cell membrane is an important site of action for this active retinoid.

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Year:  1989        PMID: 2521337

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


  11 in total

1.  Sex-dependent inhibition by retinoic acid of thyroid-hormone action on rabbit reticulocyte Ca2(+)-ATPase activity.

Authors:  F B Davis; T J Smith; P J Davis; W D Lawrence; A J Ryan; M O Farrell; S D Blas
Journal:  Biochem J       Date:  1991-01-15       Impact factor: 3.857

2.  Ethanol impairs activation of retinoic acid receptors in cerebellar granule cells in a rodent model of fetal alcohol spectrum disorders.

Authors:  Ambrish Kumar; Chandra K Singh; Donald D DiPette; Ugra S Singh
Journal:  Alcohol Clin Exp Res       Date:  2010-03-01       Impact factor: 3.455

3.  Binding of all-trans-retinoic acid to MLTC-1 proteins.

Authors:  Erika Cione; Paola Tucci; Valentina Senatore; Giuseppina Ioele; Giuseppe Genchi
Journal:  Mol Cell Biochem       Date:  2005-08       Impact factor: 3.396

4.  Retinoylation reaction of proteins in Leydig (TM-3) cells.

Authors:  Erika Cione; Paola Tucci; Adele Chimento; Vincenzo Pezzi; Giuseppe Genchi
Journal:  J Bioenerg Biomembr       Date:  2005-02       Impact factor: 2.945

5.  Ligand specificities of recombinant retinoic acid receptors RAR alpha and RAR beta.

Authors:  M Crettaz; A Baron; G Siegenthaler; W Hunziker
Journal:  Biochem J       Date:  1990-12-01       Impact factor: 3.857

6.  Retinoic acid inhibits calmodulin binding to human erythrocyte membranes and reduces membrane Ca2(+)-adenosine triphosphatase activity.

Authors:  F B Davis; T J Smith; M R Deziel; P J Davis; S D Blas
Journal:  J Clin Invest       Date:  1990-06       Impact factor: 14.808

7.  Stereochemical requirements for the modulation by retinoic acid of thyroid hormone activation of Ca(2+)-ATPase and binding at the human erythrocyte membrane.

Authors:  T J Smith; F B Davis; P J Davis
Journal:  Biochem J       Date:  1992-06-01       Impact factor: 3.857

Review 8.  The Ca(2+)-transport ATPases from the plasma membrane.

Authors:  F Wuytack; L Raeymaekers
Journal:  J Bioenerg Biomembr       Date:  1992-06       Impact factor: 2.945

9.  Characterization of rat testes mitochondrial retinoylating system and its partial purification.

Authors:  Erika Cione; Giuseppe Genchi
Journal:  J Bioenerg Biomembr       Date:  2004-04       Impact factor: 2.945

10.  Covalent modification of proteins by ligands of steroid hormone receptors.

Authors:  N Takahashi; T R Breitman
Journal:  Proc Natl Acad Sci U S A       Date:  1992-11-15       Impact factor: 11.205

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