Tetraploidization or autophagy: The ultimate fate of senescent human endometrial stem cells under ATM or p53 inhibition

Cell Cycle. 2016;15(1):117-27. doi: 10.1080/15384101.2015.1121326.

Abstract

Previously we demonstrated that endometrium-derived human mesenchymal stem cells (hMESCs) via activation of the ATM/p53/p21/Rb pathway enter the premature senescence in response to oxidative stress. Down regulation effects of the key components of this signaling pathway, particularly ATM and p53, on a fate of stressed hMESCs have not yet been investigated. In the present study by using the specific inhibitors Ku55933 and Pifithrin-α, we confirmed implication of both ATM and p53 in H(2)O(2)-induced senescence of hMESCs. ATM or p53 down regulation was shown to modulate differently the cellular fate of H(2)O(2)-treated hMESCs. ATM inhibition allowed H(2)O(2)-stimulated hMESCs to escape the permanent cell cycle arrest due to loss of the functional ATM/p53/p21/Rb pathway, and induced bypass of mitosis and re-entry into S phase, resulting in tetraploid cells. On the contrary, suppression of the p53 transcriptional activity caused a pronounced cell death of H(2)O(2)-treated hMESCs via autophagy induction. The obtained data clearly demonstrate that down regulation of ATM or p53 shifts senescence of human endometrial stem cells toward tetraploidization or autophagy.

Keywords: ATM kinase; autophagy; cellular senescence; oxidative stress; p53; stem cells; tetraploidization.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Ataxia Telangiectasia Mutated Proteins / antagonists & inhibitors
  • Ataxia Telangiectasia Mutated Proteins / metabolism*
  • Autophagy / drug effects
  • Autophagy / physiology*
  • Cell Survival / drug effects
  • Cell Survival / physiology
  • Cellular Senescence / drug effects
  • Cellular Senescence / physiology*
  • Endometrium / drug effects
  • Endometrium / metabolism*
  • Female
  • Humans
  • Hydrogen Peroxide / pharmacology
  • Mesenchymal Stem Cells / drug effects
  • Mesenchymal Stem Cells / metabolism*
  • Morpholines / pharmacology
  • Pyrones / pharmacology
  • Tetraploidy*
  • Tumor Suppressor Protein p53 / antagonists & inhibitors
  • Tumor Suppressor Protein p53 / metabolism*

Substances

  • 2-morpholin-4-yl-6-thianthren-1-yl-pyran-4-one
  • Morpholines
  • Pyrones
  • Tumor Suppressor Protein p53
  • Hydrogen Peroxide
  • ATM protein, human
  • Ataxia Telangiectasia Mutated Proteins