Vitamin B6 influences glucocorticoid receptor-dependent gene expression

J Biol Chem. 1990 Jul 25;265(21):12424-33.

Abstract

We have examined the influence of intracellular vitamin B6 concentration on glucocorticoid receptor function in HeLa S3 cells transfected with a glucocorticoid-responsive chloramphenicol acetyltransferase (CAT) reporter plasmid. CAT activity is induced from this plasmid specifically by glucocorticoid hormones in a glucocorticoid receptor-dependent manner. The intracellular concentration of pyridoxal phosphate, the physiologically active form of the vitamin, was elevated by supplementation of the culture medium with the synthesis precursor pyridoxine and lowered by exposure to the pyridoxal phosphate synthesis inhibitor 4-deoxypyridoxine. Analysis of glucocorticoid responsiveness revealed that elevated concentrations of intracellular pyridoxal phosphate suppressed the amount of glucocorticoid-induced CAT activity whereas moderate deficiency enhanced the level of glucocorticoid receptor-mediated gene expression. In contrast, modulation of the intracellular pyridoxal phosphate concentration had no effect on either basal CAT activity derived from cells not stimulated with dexamethasone or on CAT activity derived from two glucocorticoid-insensitive reporter plasmids. The modulatory effects of pyridoxal phosphate concentration occur without changes in glucocorticoid receptor mRNA levels, glucocorticoid receptor protein concentration, or the steroid binding capacity of the receptor. These observations demonstrate that vitamin B6 selectively influences glucocorticoid receptor-dependent gene expression through a novel mechanism that does not involve alterations in glucocorticoid receptor concentration or ligand binding capacity.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Gene Expression / drug effects*
  • Glucocorticoids / pharmacology
  • HeLa Cells
  • Humans
  • In Vitro Techniques
  • Plasmids
  • Promoter Regions, Genetic
  • Pyridoxal Phosphate / metabolism
  • Pyridoxine / analogs & derivatives
  • Pyridoxine / pharmacology*
  • RNA, Messenger / genetics
  • Receptors, Glucocorticoid / physiology*

Substances

  • Glucocorticoids
  • RNA, Messenger
  • Receptors, Glucocorticoid
  • Pyridoxal Phosphate
  • 4-deoxypyridoxine
  • Pyridoxine