Oxidative stress and dietary micronutrient deficiencies contribute to overexpression of epigenetically regulated genes by lupus T cells

Copyright © 2018 Elsevier Inc. All rights reserved.

Détails bibliographiques
Publié dans:Clinical immunology (Orlando, Fla.). - 1999. - 196(2018) vom: 05. Nov., Seite 97-102
Auteur principal: Ray, Donna (Auteur)
Autres auteurs: Strickland, Faith M, Richardson, Bruce C
Format: Article en ligne
Langue:English
Publié: 2018
Accès à la collection:Clinical immunology (Orlando, Fla.)
Sujets:Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Diet Lupus Oxidative stress T-lymphocytes Micronutrients Homocysteine plus... 0LVT1QZ0BA Peroxynitrous Acid 14691-52-2 Vitamin B 6 8059-24-3 Folic Acid 935E97BOY8 Methionine AE28F7PNPL DNA Modification Methylases EC 2.1.1.- Zinc J41CSQ7QDS Choline N91BDP6H0X Vitamin B 12 P6YC3EG204 Riboflavin TLM2976OFR
Description
Résumé:Copyright © 2018 Elsevier Inc. All rights reserved.
Patients with active lupus have altered T cells characterized by low DNA methyltransferase levels. We hypothesized that low DNA methyltransferase levels synergize with low methionine levels to cause greater overexpression of genes normally suppressed by DNA methylation. CD4+ T cells from lupus patients and controls were stimulated with PHA then cultured in custom media with normal or low methionine levels. Oxidative stress was induced by treating the normal CD4+ T cells with peroxynitrite prior to culture. Methylation sensitive gene expression was measured by flow cytometry. Results showed low methionine levels caused greater overexpression of methylation sensitive genes in peroxynitrite treated T cells relative to untreated T cells, and in T cells from lupus patients relative to T cells from healthy controls. In conclusion, low dietary transmethylation micronutrient levels and low DNA methyltransferase levels caused either by oxidative stress or lupus, have additive effects on methylation sensitive T cell gene expression
Description:Date Completed 14.10.2019
Date Revised 06.03.2020
published: Print-Electronic
Citation Status MEDLINE
ISSN:1521-7035
DOI:10.1016/j.clim.2018.04.003