ES cells do not activate p53-dependent stress responses and undergo p53-independent apoptosis in response to DNA damage

Curr Biol. 1998 Jan 29;8(3):145-55. doi: 10.1016/s0960-9822(98)70061-2.

Abstract

Background: Embryonic stem (ES) cells can contribute precursors to all adult cell lineages. Consequently, damage to ES cell genomes may cause serious developmental malfunctions. In somatic cells, cell-cycle checkpoints limit DNA damage by preventing DNA replication under conditions that may produce chromosomal aberrations. The tumor suppressor p53 is involved in such checkpoint controls and is also required to avoid a high rate of embryonic malformations. We characterized the cell-cycle and DNA-damage responses of ES cells to elucidate the mechanisms that prevent accumulation or transmission of damaged genomes during development.

Results: ES cells derived from wild-type mice did not undergo cell-cycle arrest in response to DNA damage or nucleotide depletion, although they synthesized abundant quantities of p53. The p53 protein in ES cells was cytoplasmic and translocated inefficiently to the nucleus upon nucleotide depletion. Expression of high levels of active p53 from an adenovirus vector could not trigger cell cycle arrest. Instead, ES cells that sustained DNA damage underwent p53-independent apoptosis. The antimetabolite-induced p53-dependent arrest response was restored in ES cells upon differentiation.

Conclusions: Cell-cycle regulatory pathways in early embryos differ significantly from those in differentiated somatic cells. In undifferentiated ES cells, p53 checkpoint pathways are compromised by factors that affect the nuclear localization of p53 and by the loss of downstream factors that are necessary to induce cell-cycle arrest. A p53-independent programmed cell death pathway is effectively employed to prevent cells with damaged genomes from contributing to the developing organism. The p53-mediated checkpoint controls become important when differentiation occurs.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Antimetabolites / pharmacology
  • Apoptosis*
  • Aspartic Acid / analogs & derivatives
  • Aspartic Acid / pharmacology
  • Cell Cycle / physiology*
  • Cell Differentiation / drug effects
  • Cell Nucleus / metabolism
  • DNA Damage*
  • Doxorubicin / pharmacology
  • Embryo, Mammalian / cytology*
  • Gamma Rays
  • Humans
  • Phosphonoacetic Acid / analogs & derivatives
  • Phosphonoacetic Acid / pharmacology
  • Stem Cells / drug effects
  • Stem Cells / metabolism*
  • Stem Cells / radiation effects
  • Transfection
  • Tretinoin
  • Tumor Suppressor Protein p53 / physiology*

Substances

  • Antimetabolites
  • Tumor Suppressor Protein p53
  • Aspartic Acid
  • Tretinoin
  • sparfosic acid
  • Doxorubicin
  • Phosphonoacetic Acid