Data from proteomic characterization of the role of Snail1 in murine mesenchymal stem cells and 3T3-L1 fibroblasts differentiation

A. Peláez-García, R. Barderas, M. Mendes, M. Lopez-Lucendo, J. C. Sanchez, A. García de Herreros, J. I. Casal*

*Corresponding author for this work

Research output: Contribution to journalArticleResearchpeer-review

5 Citations (Scopus)

Abstract

The transcription factor (TF) Snail1 is a major inducer of the epithelial-mesenchymal transition (EMT) during embryonic development and cancer progression. Ectopic expression of Snail in murine mesenchymal stem cells (mMSC) abrogated their differentiation to osteoblasts or adipocytes. We used either stable isotopic metabolic labeling (SILAC) for 3T3-L1 cells or isobaric labeling with tandem mass tags (TMT) for mMSC stably transfected cells with Snail1 or control. We carried out a proteomic analysis on the nuclear fraction since Snail is a nuclear TF that mediates its effects mainly through the regulation of other TFs. Proteomics data have been deposited in ProteomeXchange via the PRIDE partner repository with the dataset identifiers PXD001529 and PXD002157 (Vizcaino et al., 2014) [1]. Data are associated with a research article published in Molecular and Cellular Proteomics (Pelaez-Garcia et al., 2015) [2].

Original languageEnglish
Pages (from-to)606-613
Number of pages8
JournalData in Brief
Volume4
DOIs
Publication statusPublished - 1 Sept 2015
Externally publishedYes

Keywords

  • Adipogenesis
  • Differentiation
  • IL-17
  • Mesenchymal cells
  • Obesity
  • Proteomics
  • Snail
  • Transcription factors

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