Resveratrol is a natural polyphenol with several therapeutic effects, in particular, inducing p53-dependent cell cycle arrest and/or apoptosis in tumor cells. Resveratrol-induced p53 activation may trigger differentiation and apoptosis in embryonic stem cells (ESCs). We show that resveratrol activates p53 that is negatively regulated by SIRT1 deacetylation on Lys379 and positively by AMPK phosphorylation on Ser15 in mouse ESCs (mESCs). Surprisingly, the resveratrol-activated p53 is not associated with either G1/S cell cycle checkpoint or apoptosis in mESCs. Instead, it stimulates autophagy in a transcriptional-dependent manner involving up-regulation of dram1 gene expression. This study demonstrates a novel mechanism of resveratrol-dependent p53 activation in mESCs.

Original languageEnglish
Pages (from-to)2180-2185
Number of pages6
JournalBiochemical and Biophysical Research Communications
Volume503
Issue number3
DOIs
StatePublished - 10 Sep 2018
Externally publishedYes

    Research areas

  • Animals, Autophagy/drug effects, Cell Cycle Checkpoints/drug effects, Cells, Cultured, Membrane Proteins/genetics, Mice, Mouse Embryonic Stem Cells/cytology, Resveratrol/pharmacology, Tumor Suppressor Protein p53/agonists, Up-Regulation/drug effects

ID: 85161344