Identification of mouse cochlear progenitors that develop hair and supporting cells in the organ of Corti

Nat Commun. 2017 May 11:8:15046. doi: 10.1038/ncomms15046.

Abstract

The adult mammalian cochlear sensory epithelium houses two major types of cells, mechanosensory hair cells and underlying supporting cells, and lacks regenerative capacity. Recent evidence indicates that a subset of supporting cells can spontaneously regenerate hair cells after ablation only within the first week postparturition. Here in vivo clonal analysis of mouse inner ear cells during development demonstrates clonal relationship between hair and supporting cells in sensory organs. We report the identification in mouse of a previously unknown population of multipotent stem/progenitor cells that are capable of not only contributing to the hair and supporting cells but also to other cell types, including glia, in cochlea undergoing development, maturation and repair in response to damage. These multipotent progenitors originate from Eya1-expressing otic progenitors. Our findings also provide evidence for detectable regenerative potential in the postnatal cochlea beyond 1 week of age.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Newborn
  • Basic Helix-Loop-Helix Transcription Factors / genetics
  • Basic Helix-Loop-Helix Transcription Factors / metabolism
  • Biomarkers / metabolism
  • Cell Differentiation
  • Embryo, Mammalian
  • Female
  • Gene Expression
  • Genes, Reporter
  • Green Fluorescent Proteins / genetics
  • Green Fluorescent Proteins / metabolism
  • Hair Cells, Auditory / cytology*
  • Hair Cells, Auditory / metabolism
  • Hearing / physiology*
  • Intracellular Signaling Peptides and Proteins / genetics
  • Intracellular Signaling Peptides and Proteins / metabolism
  • Labyrinth Supporting Cells / cytology*
  • Labyrinth Supporting Cells / metabolism
  • Luminescent Proteins / genetics
  • Luminescent Proteins / metabolism
  • Male
  • Mice
  • Multipotent Stem Cells / cytology*
  • Multipotent Stem Cells / metabolism
  • Myosin VIIa
  • Myosins / genetics
  • Myosins / metabolism
  • Neuroglia / cytology*
  • Neuroglia / metabolism
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism
  • Protein Tyrosine Phosphatases / genetics
  • Protein Tyrosine Phosphatases / metabolism
  • Red Fluorescent Protein

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • Biomarkers
  • Cyan Fluorescent Protein
  • Intracellular Signaling Peptides and Proteins
  • Luminescent Proteins
  • Myo7a protein, mouse
  • Myosin VIIa
  • Neurod1 protein, mouse
  • Nuclear Proteins
  • Green Fluorescent Proteins
  • Eya1 protein, mouse
  • Protein Tyrosine Phosphatases
  • Myosins