4.7 Article

Repression of Igf1 expression by Ezh2 prevents basal cell differentiation in the developing lung

期刊

DEVELOPMENT
卷 142, 期 8, 页码 1458-1469

出版社

COMPANY BIOLOGISTS LTD
DOI: 10.1242/dev.122077

关键词

Polycomb repressive complex 2; Ezh2; Lung development; Basal cells; IGF1; Mouse

资金

  1. Australian Research Council Queen Elizabeth II Fellowships
  2. Elizabeth and Vernon Puzey Scholarship from the University of Melbourne
  3. Strathmore Community College Scholarship
  4. Australian National Health and Medical Research Council grant [APP1079756]

向作者/读者索取更多资源

Epigenetic mechanisms involved in the establishment of lung epithelial cell lineage identities during development are largely unknown. Here, we explored the role of the histone methyltransferase Ezh2 during lung lineage determination. Loss of Ezh2 in the lung epithelium leads to defective lung formation and perinatal mortality. We show that Ezh2 is crucial for airway lineage specification and alveolarization. Using optical projection tomography imaging, we found that branching morphogenesis is affected in Ezh2 conditional knockout mice and the remaining bronchioles are abnormal, lacking terminally differentiated secretory club cells. Remarkably, RNA-seq analysis revealed the upregulation of basal genes in Ezh2-deficient epithelium. Three-dimensional imaging for keratin 5 further showed the unexpected presence of a layer of basal cells from the proximal airways to the distal bronchioles in E16.5 embryos. ChIP-seq analysis indicated the presence of Ezh2-mediated repressive marks on the genomic loci of some but not all basal genes, suggesting an indirect mechanism of action of Ezh2. We found that loss of Ezh2 de-represses insulin-like growth factor 1 (Igf1) expression and that modulation of IGF1 signaling ex vivo in wild-type lungs could induce basal cell differentiation. Altogether, our work reveals an unexpected role for Ezh2 in controlling basal cell fate determination in the embryonic lung endoderm, mediated in part by repression of Igf1 expression.

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