Transcription factor NF-Y inhibits cell growth and decreases SOX2 expression in human embryonal carcinoma cell line NT2/D1

Biochemistry (Mosc). 2015 Feb;80(2):202-7. doi: 10.1134/S0006297915020066.

Abstract

Transcription factor NF-Y belongs to the embryonic stem cell transcription factor circuitry due to its role in the regulation of cell proliferation. We investigated the role of NF-Y in pluripotency maintenance using NT2/D1 cells as one of the best-characterized human embryonal carcinoma cell line. We investigated the efficiency of protein transduction and analyzed the effects of forced expression of short isoform of NF-Y A-subunit (NF-YAs) on NT2/D1 cell growth and expression of SOX2. We found that protein transduction is an efficient method for NF-Y overexpression in NT2/D1 cells. Next, we analyzed the effect of NF-YAs overexpression on NT2/D1 cell viability and detected significant reduction in cell growth. The negative effect of NF-YAs overexpression on NT2/D1 cell pluripotency maintenance was confirmed by the decrease in the level of the pluripotency marker SOX2. Finally, we checked the p53 status and determined that the NF-Y-induced inhibition of NT2/D1 cell growth is p53-independent.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • CCAAT-Binding Factor / physiology*
  • Cell Line, Tumor
  • Cell Proliferation
  • Embryonal Carcinoma Stem Cells
  • Gene Expression
  • Humans
  • Pluripotent Stem Cells / metabolism*
  • SOXB1 Transcription Factors / genetics*
  • Tumor Suppressor Protein p53 / genetics

Substances

  • CCAAT-Binding Factor
  • NFYA protein, human
  • SOX2 protein, human
  • SOXB1 Transcription Factors
  • Tumor Suppressor Protein p53