Genomic and proteomic profiling of oxidative stress response in human diploid fibroblasts

Biogerontology. 2009 Apr;10(2):125-51. doi: 10.1007/s10522-008-9157-3. Epub 2008 Jul 25.

Abstract

A number of lines of evidence suggest that senescence of normal human diploid fibroblasts (HDFs) in culture is relevant to the process of aging in vivo. Using normal human skin diploid fibroblasts, we examine the changes in genes and proteins following treatment with a mild dose of H2O2, which induces premature senescence. Multidimensional Protein Identification Technology (MudPIT) in combination with mass spectrometry analyses of whole cell lysates from HDFs detected 65 proteins in control group, 48 proteins in H2O2-treated cells and 109 proteins common in both groups. In contrast, cDNA microarray analyses show 173 genes up-regulated and 179 genes down-regulated upon H2O2 treatment. Both MudPIT and cDNA microarray analyses indicate that H2O2 treatment caused elevated levels of thioredoxin reductase 1. Semi-quantitative RT-PCR and Western-blot were able to verify the finding. Out of a large number of genes or proteins detected, only a small fraction shows the overlap between the outcomes of microarray versus proteomics. The low overlap suggests the importance of considering proteins instead of transcripts when investigating the gene expression profile altered by oxidative stress.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Amino Acid Sequence
  • Blotting, Western
  • Cells, Cultured
  • Cellular Senescence / drug effects
  • Cellular Senescence / genetics*
  • Chromatography, High Pressure Liquid
  • Diploidy*
  • Fibroblasts / drug effects
  • Fibroblasts / metabolism*
  • Gene Expression Profiling* / methods
  • Gene Regulatory Networks
  • Humans
  • Hydrogen Peroxide / pharmacology
  • Molecular Sequence Data
  • Oligonucleotide Array Sequence Analysis
  • Oxidative Stress / drug effects
  • Oxidative Stress / genetics*
  • Proteomics* / methods
  • Reverse Transcriptase Polymerase Chain Reaction
  • Tandem Mass Spectrometry
  • Thioredoxin Reductase 1 / genetics
  • Thioredoxin Reductase 1 / metabolism

Substances

  • Hydrogen Peroxide
  • TXNRD1 protein, human
  • Thioredoxin Reductase 1