[3H]-13-cis-retinoic acid covalently binds to thioredoxin reductase in human keratinocytes
- PMID: 2064786
- DOI: 10.1159/000210919
[3H]-13-cis-retinoic acid covalently binds to thioredoxin reductase in human keratinocytes
Abstract
13-cis-Retinoic acid is a stereospecific suicide inhibitor of thioredoxin reductase. [3H]-labeled 13-cis-retinoic acid has been used to covalently label thioredoxin reductase in human keratinocytes. The acid-soluble cytosol fraction of human keratinocytes contained three radioactive proteins labeled by the addition of high-specific-activity [3H]-13-cis-retinoic acid to cell cultures. One of these proteins was identified as cytosolic keratinocyte thioredoxin reductase by fast-protein liquid chromatography and SDS-gel radioautography. The inhibition of thioredoxin reductase by 13-cis-retinoic acid may explain the known cytostatic and teratogenic properties attributed to this retinoid.
Similar articles
-
The stereospecific suicide inhibition of human melanoma thioredoxin reductase by 13-cis-retinoic acid.Biochem Biophys Res Commun. 1989 Apr 28;160(2):573-9. doi: 10.1016/0006-291x(89)92471-6. Biochem Biophys Res Commun. 1989. PMID: 2719682
-
All-trans-retinoic acid and 13-cis-retinoic acid: pharmacokinetics and biological activity in different cell culture models of human keratinocytes.Horm Metab Res. 2007 Feb;39(2):136-40. doi: 10.1055/s-2007-961813. Horm Metab Res. 2007. PMID: 17326009
-
all-trans-retinoic acid regulates retinol and 3,4-didehydroretinol metabolism in cultured human epidermal keratinocytes.J Invest Dermatol. 1996 Jan;106(1):168-75. doi: 10.1111/1523-1747.ep12329900. J Invest Dermatol. 1996. PMID: 8592069
-
Ultraviolet irradiation depletes cellular retinol and alters the metabolism of retinoic acid in cultured human keratinocytes and melanocytes.Melanoma Res. 1999 Aug;9(4):339-46. doi: 10.1097/00008390-199908000-00001. Melanoma Res. 1999. PMID: 10504051
-
Hsp90 and Thioredoxin-Thioredoxin Reductase enable the catalytic activity of Clostridial neurotoxins inside nerve terminals.Toxicon. 2018 Jun 1;147:32-37. doi: 10.1016/j.toxicon.2017.10.028. Epub 2017 Oct 28. Toxicon. 2018. PMID: 29111118 Review.
Cited by
-
Covalent modification of proteins by ligands of steroid hormone receptors.Proc Natl Acad Sci U S A. 1992 Nov 15;89(22):10807-11. doi: 10.1073/pnas.89.22.10807. Proc Natl Acad Sci U S A. 1992. PMID: 1438281 Free PMC article.
-
Nuclear MEK1 sequesters PPARγ and bisects MEK1/ERK signaling: a non-canonical pathway of retinoic acid inhibition of adipocyte differentiation.PLoS One. 2014 Jun 24;9(6):e100862. doi: 10.1371/journal.pone.0100862. eCollection 2014. PLoS One. 2014. PMID: 24959884 Free PMC article.