Dose-dependent modulation of the T cell proteome by ascorbic acid

Br J Nutr. 2007 Jan;97(1):19-26. doi: 10.1017/S0007114507197592.

Abstract

To investigate the hypothesis that the micronutrient ascorbic acid can modulate the functional genome, T cells (CCRF-HSB2) were treated with ascorbic acid (up to 150 microM) for up to 24 h. Protein expression changes were assessed by two-dimensional electrophoresis. Forty-one protein spots which showed greater than two-fold expression changes were subject to identification by matrix-assisted laser desorption ionisation time of flight MS. The confirmed protein identifications were clustered into five groups; proteins were associated with signalling, carbohydrate metabolism, apoptosis, transcription and immune function. The increased expression of phosphatidylinositol transfer protein (promotes intracellular signalling) within 5 min of ascorbic acid treatment was confirmed by Western blotting. Together, these observations suggest that ascorbic acid modulates the T cell proteome in a time- and dose-dependent manner and identify molecular targets for study following antioxidant supplementation in vivo.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Ascorbic Acid / pharmacology*
  • Blotting, Western / methods
  • Cell Line, Transformed
  • DNA Fingerprinting
  • Dose-Response Relationship, Drug
  • Electrophoresis, Gel, Two-Dimensional
  • Humans
  • Phospholipid Transfer Proteins / genetics
  • Phospholipid Transfer Proteins / metabolism
  • Proteome / drug effects*
  • Proteome / genetics
  • Proteome / metabolism
  • Signal Transduction / drug effects*
  • Signal Transduction / genetics
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
  • T-Lymphocytes / chemistry*
  • T-Lymphocytes / drug effects
  • T-Lymphocytes / metabolism
  • Time Factors

Substances

  • Phospholipid Transfer Proteins
  • Proteome
  • Ascorbic Acid