Combinatorial Atoh1 and Gfi1 induction enhances hair cell regeneration in the adult cochlea
Abstract Mature mammalian cochlear hair cells (HCs) do not spontaneously regenerate once lost, leading to life-long hearing deficits. Attempts to induce HC regeneration in adult mammals have used over-expression of the HC-specific transcription factor Atoh1, but to date this approach has yielded low...
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doaj-a5f302ca620148b1ae8d55867529301b2020-12-13T12:34:09ZengNature Publishing GroupScientific Reports2045-23222020-12-0110111510.1038/s41598-020-78167-8Combinatorial Atoh1 and Gfi1 induction enhances hair cell regeneration in the adult cochleaSungsu Lee0Jae-Jun Song1Lisa A. Beyer2Donald L. Swiderski3Diane M. Prieskorn4Melih Acar5Hsin-I Jen6Andrew K. Groves7Yehoash Raphael8Kresge Hearing Research Institute, Department of Otolaryngology-Head and Neck Surgery, The University of MichiganDepartment of Otolaryngology-Head and Neck Surgery, Korea University College of MedicineKresge Hearing Research Institute, Department of Otolaryngology-Head and Neck Surgery, The University of MichiganKresge Hearing Research Institute, Department of Otolaryngology-Head and Neck Surgery, The University of MichiganKresge Hearing Research Institute, Department of Otolaryngology-Head and Neck Surgery, The University of MichiganDepartment of Medical Biology, School of Medicine, Bahcesehir UniversityDepartment of Neuroscience, Baylor College of MedicineDepartment of Neuroscience, Baylor College of MedicineKresge Hearing Research Institute, Department of Otolaryngology-Head and Neck Surgery, The University of MichiganAbstract Mature mammalian cochlear hair cells (HCs) do not spontaneously regenerate once lost, leading to life-long hearing deficits. Attempts to induce HC regeneration in adult mammals have used over-expression of the HC-specific transcription factor Atoh1, but to date this approach has yielded low and variable efficiency of HC production. Gfi1 is a transcription factor important for HC development and survival. We evaluated the combinatorial effects of Atoh1 and Gfi1 over-expression on HC regeneration using gene transfer methods in neonatal cochlear explants, and in vivo in adult mice. Adenoviral over-expression of Atoh1 and Gfi1 in cultured neonatal cochlear explants resulted in numerous ectopic HC-like cells (HCLCs), with significantly more cells in Atoh1 + Gfi1 cultures than Atoh1 alone. In vitro, ectopic HCLCs emerged in regions medial to inner HCs as well as in the stria vascularis. In vivo experiments were performed in mature Pou4f3DTR mice in which HCs were completely and specifically ablated by administration of diphtheria toxin. Adenoviral expression of Atoh1 or Atoh1 + Gfi1 in cochlear supporting cells induced appearance of HCLCs, with Atoh1 + Gfi1 expression leading to 6.2-fold increase of new HCLCs after 4 weeks compared to Atoh1 alone. New HCLCs were detected throughout the cochlea, exhibited immature stereocilia and survived for at least 8 weeks. Combinatorial Atoh1 and Gfi1 induction is thus a promising strategy to promote HC regeneration in the mature mammalian cochlea.https://doi.org/10.1038/s41598-020-78167-8 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Sungsu Lee Jae-Jun Song Lisa A. Beyer Donald L. Swiderski Diane M. Prieskorn Melih Acar Hsin-I Jen Andrew K. Groves Yehoash Raphael |
spellingShingle |
Sungsu Lee Jae-Jun Song Lisa A. Beyer Donald L. Swiderski Diane M. Prieskorn Melih Acar Hsin-I Jen Andrew K. Groves Yehoash Raphael Combinatorial Atoh1 and Gfi1 induction enhances hair cell regeneration in the adult cochlea Scientific Reports |
author_facet |
Sungsu Lee Jae-Jun Song Lisa A. Beyer Donald L. Swiderski Diane M. Prieskorn Melih Acar Hsin-I Jen Andrew K. Groves Yehoash Raphael |
author_sort |
Sungsu Lee |
title |
Combinatorial Atoh1 and Gfi1 induction enhances hair cell regeneration in the adult cochlea |
title_short |
Combinatorial Atoh1 and Gfi1 induction enhances hair cell regeneration in the adult cochlea |
title_full |
Combinatorial Atoh1 and Gfi1 induction enhances hair cell regeneration in the adult cochlea |
title_fullStr |
Combinatorial Atoh1 and Gfi1 induction enhances hair cell regeneration in the adult cochlea |
title_full_unstemmed |
Combinatorial Atoh1 and Gfi1 induction enhances hair cell regeneration in the adult cochlea |
title_sort |
combinatorial atoh1 and gfi1 induction enhances hair cell regeneration in the adult cochlea |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2020-12-01 |
description |
Abstract Mature mammalian cochlear hair cells (HCs) do not spontaneously regenerate once lost, leading to life-long hearing deficits. Attempts to induce HC regeneration in adult mammals have used over-expression of the HC-specific transcription factor Atoh1, but to date this approach has yielded low and variable efficiency of HC production. Gfi1 is a transcription factor important for HC development and survival. We evaluated the combinatorial effects of Atoh1 and Gfi1 over-expression on HC regeneration using gene transfer methods in neonatal cochlear explants, and in vivo in adult mice. Adenoviral over-expression of Atoh1 and Gfi1 in cultured neonatal cochlear explants resulted in numerous ectopic HC-like cells (HCLCs), with significantly more cells in Atoh1 + Gfi1 cultures than Atoh1 alone. In vitro, ectopic HCLCs emerged in regions medial to inner HCs as well as in the stria vascularis. In vivo experiments were performed in mature Pou4f3DTR mice in which HCs were completely and specifically ablated by administration of diphtheria toxin. Adenoviral expression of Atoh1 or Atoh1 + Gfi1 in cochlear supporting cells induced appearance of HCLCs, with Atoh1 + Gfi1 expression leading to 6.2-fold increase of new HCLCs after 4 weeks compared to Atoh1 alone. New HCLCs were detected throughout the cochlea, exhibited immature stereocilia and survived for at least 8 weeks. Combinatorial Atoh1 and Gfi1 induction is thus a promising strategy to promote HC regeneration in the mature mammalian cochlea. |
url |
https://doi.org/10.1038/s41598-020-78167-8 |
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