Ezh2 represses the basal cell lineage during lung endoderm development

Development. 2015 Jan 1;142(1):108-17. doi: 10.1242/dev.116947.

Abstract

The development of the lung epithelium is regulated in a stepwise fashion to generate numerous differentiated and stem cell lineages in the adult lung. How these different lineages are generated in a spatially and temporally restricted fashion remains poorly understood, although epigenetic regulation probably plays an important role. We show that the Polycomb repressive complex 2 component Ezh2 is highly expressed in early lung development but is gradually downregulated by late gestation. Deletion of Ezh2 in early lung endoderm progenitors leads to the ectopic and premature appearance of Trp63+ basal cells that extend the entire length of the airway. Loss of Ezh2 also leads to reduced secretory cell differentiation. In their place, morphologically similar cells develop that express a subset of basal cell genes, including keratin 5, but no longer express high levels of either Trp63 or of standard secretory cell markers. This suggests that Ezh2 regulates the phenotypic switch between basal cells and secretory cells. Together, these findings show that Ezh2 restricts the basal cell lineage during normal lung endoderm development to allow the proper patterning of epithelial lineages during lung formation.

Keywords: Basal cell; Endoderm; Lung; Mouse.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Biomarkers / metabolism
  • Cell Differentiation / genetics
  • Cell Lineage* / genetics
  • Cell Proliferation
  • Endoderm / cytology*
  • Endoderm / embryology*
  • Enhancer of Zeste Homolog 2 Protein
  • Epithelial Cells / cytology
  • Epithelial Cells / metabolism
  • Epithelium / embryology
  • Epithelium / metabolism
  • Gene Expression Profiling
  • Gene Expression Regulation, Developmental
  • Gene Ontology
  • Goblet Cells / cytology
  • Goblet Cells / metabolism
  • Hedgehog Proteins / metabolism
  • Keratin-5 / metabolism
  • Lung / cytology*
  • Lung / embryology*
  • Lung / metabolism
  • Mice
  • Mutation / genetics
  • Neuroendocrine Cells / cytology
  • Neuroendocrine Cells / metabolism
  • Nuclear Proteins / metabolism
  • Oligonucleotide Array Sequence Analysis
  • Phosphoproteins / metabolism
  • Polycomb Repressive Complex 2 / metabolism*
  • Software
  • Thyroid Nuclear Factor 1
  • Trans-Activators / metabolism
  • Transcription Factors / metabolism

Substances

  • Biomarkers
  • Hedgehog Proteins
  • Keratin-5
  • Nuclear Proteins
  • Phosphoproteins
  • Shh protein, mouse
  • Thyroid Nuclear Factor 1
  • Trans-Activators
  • Transcription Factors
  • Trp63 protein, mouse
  • Enhancer of Zeste Homolog 2 Protein
  • Ezh2 protein, mouse
  • Polycomb Repressive Complex 2