Newly expressed proteins of mouse embryonic fibroblasts irradiated to be inactive

Biochem Biophys Res Commun. 2004 Mar 12;315(3):581-8. doi: 10.1016/j.bbrc.2004.01.089.

Abstract

It has been found that post-radiation mouse embryonic fibroblasts can well maintain the pluripotency in human embryonic stem cells. However, the molecular mechanism remains unclear. In the present study, the new protein expression profile of post-radiation mouse embryonic fibroblasts was analyzed by immobilized pH gradient 2-dimensional polyacrylamide gel electrophoresis. Image analysis following silver staining revealed (969+/-57) vs. (1085+/-107) spots from post-radiation mouse embryonic fibroblasts and pre-radiation ones, respectively. Some newly expressed proteins, which were only abundantly present after irradiation, were subjected to peptide mass fingerprint analysis and identified using MALDI-TOF-MS, SWISS-PROT database, and RT-PCR. Several of those proteins were preliminarily identified to participate in cytokine secretion, cell signal transduction, transcriptional regulation, and apoptosis, etc., which suggested that inactive post-radiation mouse embryonic fibroblasts expressed some new proteins that may underlie the molecular mechanisms to maintain the pluripotency in human embryonic stem cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ADAM Proteins
  • Animals
  • Blastocyst / cytology
  • Cell Culture Techniques / methods
  • Databases, Protein
  • Electrophoresis, Gel, Two-Dimensional
  • Embryo, Mammalian / cytology
  • Female
  • Fibroblasts / cytology
  • Fibroblasts / metabolism*
  • Fibroblasts / radiation effects*
  • Gamma Rays
  • Gene Expression / radiation effects*
  • Humans
  • Integrins / biosynthesis*
  • Male
  • Mice
  • Mice, Inbred Strains
  • Mice, SCID
  • Pregnancy
  • Protein Biosynthesis*
  • Proteins*
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization / methods
  • Stem Cells / cytology
  • Tumor Suppressor Proteins / biosynthesis*
  • Wnt Proteins
  • Wnt3 Protein

Substances

  • Integrins
  • Proteins
  • Tumor Suppressor Proteins
  • Wnt Proteins
  • Wnt3 Protein
  • ADAM Proteins
  • ADAM11 protein, human