Temporal quantitative proteomics by iTRAQ 2D-LC-MS/MS and corresponding mRNA expression analysis identify post-transcriptional modulation of actin-cytoskeleton regulators during TGF-beta-Induced epithelial-mesenchymal transition

J Proteome Res. 2009 Jan;8(1):35-47. doi: 10.1021/pr8006478.

Abstract

To gain insights into how TGF-beta regulates epithelial-mesenchymal transition (EMT), we assessed the time course of proteins and mRNAs during EMT by multiplex iTRAQ labeling and 2D-LC-MS/MS, and by hybridization, respectively. Temporal iTRAQ analysis identified 66 proteins as differentially expressed during EMT, including newly associated proteins calpain, fascin and macrophage-migration inhibitory factor (MIF). Comparing protein and mRNA expression overtime showed that all the 14 up-regulated proteins involved in the actin-cytoskeleton remodeling were accompanied by increases in corresponding mRNA expression. Interestingly, siRNA mediated knockdown of cofilin1 potentiated TGF-beta-induced EMT. Further analysis of cofilin1 and beta-actin revealed an increase in their mRNA stability in response to TGF-beta, contributing to the observed increase in mRNA and protein expression. These results are the first demonstration of post-transcriptional regulation of cytoskeletal remodelling and a key role for cofilin1 during TGF-beta-induced EMT.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / metabolism*
  • Cell Differentiation / drug effects
  • Cell Line, Tumor
  • Chromatography, Liquid / methods*
  • Cofilin 1 / metabolism
  • Cytoskeleton / metabolism*
  • Epithelium / drug effects*
  • Gene Expression Regulation
  • Humans
  • Mass Spectrometry / methods*
  • Mesoderm / drug effects*
  • Proteomics / methods*
  • RNA Processing, Post-Transcriptional*
  • RNA, Messenger / metabolism*
  • Time Factors
  • Transforming Growth Factor beta / metabolism*

Substances

  • Actins
  • Cofilin 1
  • RNA, Messenger
  • Transforming Growth Factor beta