Cochlear progenitor number is controlled through mesenchymal FGF receptor signaling

Author:

Huh Sung-Ho1,Warchol Mark E2,Ornitz David M1ORCID

Affiliation:

1. Department of Developmental Biology, Washington University School of Medicine, St Louis, United States

2. Department of Otolaryngology, Washington University School of Medicine, St Louis, United States

Abstract

The sensory and supporting cells (SCs) of the organ of Corti are derived from a limited number of progenitors. The mechanisms that regulate the number of sensory progenitors are not known. Here, we show that Fibroblast Growth Factors (FGF) 9 and 20, which are expressed in the non-sensory (Fgf9) and sensory (Fgf20) epithelium during otic development, regulate the number of cochlear progenitors. We further demonstrate that Fgf receptor (Fgfr) 1 signaling within the developing sensory epithelium is required for the differentiation of outer hair cells and SCs, while mesenchymal FGFRs regulate the size of the sensory progenitor population and the overall cochlear length. In addition, ectopic FGFR activation in mesenchyme was sufficient to increase sensory progenitor proliferation and cochlear length. These data define a feedback mechanism, originating from epithelial FGF ligands and mediated through periotic mesenchyme that controls the number of sensory progenitors and the length of the cochlea.

Funder

Action on Hearing Loss

March of Dimes Foundation (March of Dimes Births Defect Foundation)

National Institutes of Health (NIH)

Hearing Health Foundation (HHF)

Office of Naval Research (ONR)

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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