Symmetrical and asymmetrical division analysis provides evidence for a hierarchy of prostate epithelial cell lineages

Nat Commun. 2014 Aug 28:5:4758. doi: 10.1038/ncomms5758.

Abstract

Although symmetrical and asymmetrical divisions of stem cells have been extensively studied in invertebrate and mammalian neural epithelia, their role remains largely unknown in mammalian non-neural epithelial development, regeneration and tumorigenesis. Here, using basal and luminal cell-specific markers and cell lineage tracing transgenic mice, we report that in developing prostatic epithelia, basal and luminal cells exhibit distinct division modes. While basal cells display both symmetric and asymmetric divisions leading to different cell fates, luminal cells only exhibit symmetrical divisions. Examination of cell division modes in prostate-specific Pten-null mice indicates that both luminal and basal cells can be cellular origins for prostate cancer. Furthermore, analysis of Sox2-expressing cells in p63 and Pten-null mice suggests that basal cells contribute to the luminal population and tumorigenesis. These findings provide direct evidence for the existence of a hierarchy of epithelial cell lineages during prostate development, regeneration and tumorigenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Division
  • Cell Lineage*
  • Cell Polarity / genetics
  • Epithelial Cells / cytology
  • Inhibitor of Apoptosis Proteins / metabolism
  • Male
  • Mice, Inbred BALB C
  • Mice, Mutant Strains
  • Mice, Transgenic
  • PTEN Phosphohydrolase / genetics
  • Phosphoproteins / genetics
  • Prostate / cytology*
  • Prostate / physiology
  • Repressor Proteins / metabolism
  • SOXB1 Transcription Factors / metabolism
  • Survivin
  • Trans-Activators / genetics

Substances

  • Birc5 protein, mouse
  • Inhibitor of Apoptosis Proteins
  • Phosphoproteins
  • Repressor Proteins
  • SOXB1 Transcription Factors
  • Sox2 protein, mouse
  • Survivin
  • Trans-Activators
  • Trp63 protein, mouse
  • PTEN Phosphohydrolase
  • Pten protein, mouse