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Single cell transcriptomic analysis reveals cellular diversity of murine esophageal epithelium.

Mohammad Faujul KabirAdam L KaramiRicardo Cruz-AcuñaAlena KlochkovaReshu SaxenaAnbin MuMary Grace MurrayJasmine CruzAnnie D FullerMargarette H ClevengerKumaraswamy Naidu ChitralaYinfei TanKelsey KeithJozef MadzoHugh HuangJaroslav JelinekTatiana A KarakashevaKathryn E HamiltonAmanda B MuirMarie-Pier TétreaultKelly A Whelan
Published in: Nature communications (2022)
Although morphologic progression coupled with expression of specific molecular markers has been characterized along the esophageal squamous differentiation gradient, the molecular heterogeneity within cell types along this trajectory has yet to be classified at the single cell level. To address this knowledge gap, we perform single cell RNA-sequencing of 44,679 murine esophageal epithelial, to identify 11 distinct cell populations as well as pathways alterations along the basal-superficial axis and in each individual population. We evaluate the impact of aging upon esophageal epithelial cell populations and demonstrate age-associated mitochondrial dysfunction. We compare single cell transcriptomic profiles in 3D murine organoids and human esophageal biopsies with that of murine esophageal epithelium. Finally, we employ pseudotemporal trajectory analysis to develop a working model of cell fate determination in murine esophageal epithelium. These studies provide comprehensive molecular perspective on the cellular heterogeneity of murine esophageal epithelium in the context of homeostasis and aging.
Keyphrases
  • single cell
  • rna seq
  • high throughput
  • healthcare
  • endothelial cells
  • stem cells
  • cell fate
  • poor prognosis
  • mesenchymal stem cells
  • high grade
  • single molecule
  • induced pluripotent stem cells
  • binding protein