Single-cell transcriptomic profiling of the zebrafish inner ear reveals molecularly distinct hair cell and supporting cell subtypes

Author:

Shi Tuo12ORCID,Beaulieu Marielle O3ORCID,Saunders Lauren M4ORCID,Fabian Peter1,Trapnell Cole4,Segil Neil12ORCID,Crump J Gage1ORCID,Raible David W345ORCID

Affiliation:

1. Department of Stem Cell Biology and Regenerative Medicine, Keck School of Medicine, University of Southern California

2. Caruso Department of Otolaryngology-Head and Neck Surgery, Keck School of Medicine, University of Southern California

3. Department of Otolaryngology-Head and Neck Surgery, University of Washington

4. Department of Genome Sciences, University of Washington

5. Department of Biological Structure, University of Washington

Abstract

A major cause of human deafness and vestibular dysfunction is permanent loss of the mechanosensory hair cells of the inner ear. In non-mammalian vertebrates such as zebrafish, regeneration of missing hair cells can occur throughout life. While a comparative approach has the potential to reveal the basis of such differential regenerative ability, the degree to which the inner ears of fish and mammals share common hair cells and supporting cell types remains unresolved. Here, we perform single-cell RNA sequencing of the zebrafish inner ear at embryonic through adult stages to catalog the diversity of hair cells and non-sensory supporting cells. We identify a putative progenitor population for hair cells and supporting cells, as well as distinct hair and supporting cell types in the maculae versus cristae. The hair cell and supporting cell types differ from those described for the lateral line system, a distributed mechanosensory organ in zebrafish in which most studies of hair cell regeneration have been conducted. In the maculae, we identify two subtypes of hair cells that share gene expression with mammalian striolar or extrastriolar hair cells. In situ hybridization reveals that these hair cell subtypes occupy distinct spatial domains within the three macular organs, the utricle, saccule, and lagena, consistent with the reported distinct electrophysiological properties of hair cells within these domains. These findings suggest that primitive specialization of spatially distinct striolar and extrastriolar hair cells likely arose in the last common ancestor of fish and mammals. The similarities of inner ear cell type composition between fish and mammals validate zebrafish as a relevant model for understanding inner ear-specific hair cell function and regeneration.

Funder

National Institute on Deafness and Other Communication Disorders

Hamilton and Mildred Kellogg Trust

The Whitcraft Family Gift

Hearing Health Foundation

Paul G. Allen Frontiers Group

National Human Genome Research Institute

National Institute of Dental and Craniofacial Research

Publisher

eLife Sciences Publications, Ltd

Subject

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

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