Proteomic alterations in progeny of irradiated human liver cells

J Toxicol Environ Health A. 2010;73(7):520-8. doi: 10.1080/15287390903523501.

Abstract

This study was designed to characterize the differential protein expression in the progeny of human liver cells surviving exposure to ionizing radiation. The progeny of irradiated cells were derived from a human liver cell line exposed to 0, 2, 4, or 6 Gy of (60)Co gamma-irradiation. Total protein of the cells was extracted by two-dimensional electrophoresis (2-DE) and analyzed with ImageMaster 2D Platinum software. In total, 42 differentially expressed proteins from the progeny of irradiated cells were screened, of which 17 were identified by matrix assistant laser desorption ion-top flight-mass spectrometry (MALDI-TOF-MS) analysis. There were 4 upregulated and 13 downregulated proteins detected. The upregulated expression of two proteins, mitochondrial heat-shock 60-kD protein (HSP60) and globin transcription factor 1 (GATA-1), was further confirmed by immunoblotting. Database search revealed that these differentially expressed proteins may function in cell cycle regulation, cytoskeleton maintenance, stress response, and tumor metastasis, indicating an effect of radiation-induced genomic instability (RIGI) in the progeny of irradiated cells. Analysis on functional roles of the screened proteins may provide insight into further mechanistic investigations underlying molecular events induced by RIGI.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line
  • Chaperonin 60 / metabolism
  • Dose-Response Relationship, Radiation
  • Down-Regulation / radiation effects
  • Electrophoresis, Gel, Two-Dimensional
  • GATA1 Transcription Factor / metabolism
  • Genomic Instability / radiation effects
  • Humans
  • Liver / cytology
  • Liver / metabolism
  • Liver / radiation effects*
  • Proteome / metabolism
  • Proteome / radiation effects*
  • Up-Regulation / radiation effects

Substances

  • Chaperonin 60
  • GATA1 Transcription Factor
  • Proteome