Cargando…

Dual expression of Atoh1 and Ikzf2 promotes transformation of adult cochlear supporting cells into outer hair cells

Mammalian cochlear outer hair cells (OHCs) are essential for hearing. Severe hearing impairment follows OHC degeneration. Previous attempts at regenerating new OHCs from cochlear supporting cells (SCs) have been unsuccessful, notably lacking expression of the key OHC motor protein, Prestin. Thus, re...

Descripción completa

Detalles Bibliográficos
Autores principales: Sun, Suhong, Li, Shuting, Luo, Zhengnan, Ren, Minhui, He, Shunji, Wang, Guangqin, Liu, Zhiyong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8439656/
https://www.ncbi.nlm.nih.gov/pubmed/34477109
http://dx.doi.org/10.7554/eLife.66547
_version_ 1783752551975354368
author Sun, Suhong
Li, Shuting
Luo, Zhengnan
Ren, Minhui
He, Shunji
Wang, Guangqin
Liu, Zhiyong
author_facet Sun, Suhong
Li, Shuting
Luo, Zhengnan
Ren, Minhui
He, Shunji
Wang, Guangqin
Liu, Zhiyong
author_sort Sun, Suhong
collection PubMed
description Mammalian cochlear outer hair cells (OHCs) are essential for hearing. Severe hearing impairment follows OHC degeneration. Previous attempts at regenerating new OHCs from cochlear supporting cells (SCs) have been unsuccessful, notably lacking expression of the key OHC motor protein, Prestin. Thus, regeneration of Prestin+ OHCs represents a barrier to restore auditory function in vivo. Here, we reported the successful in vivo conversion of adult mouse cochlear SCs into Prestin+ OHC-like cells through the concurrent induction of two key transcriptional factors known to be necessary for OHC development: Atoh1 and Ikzf2. Single-cell RNA sequencing revealed the upregulation of 729 OHC genes and downregulation of 331 SC genes in OHC-like cells. The resulting differentiation status of these OHC-like cells was much more advanced than previously achieved. This study thus established an efficient approach to induce the regeneration of Prestin+ OHCs, paving the way for in vivo cochlear repair via SC transdifferentiation.
format Online
Article
Text
id pubmed-8439656
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-84396562021-09-15 Dual expression of Atoh1 and Ikzf2 promotes transformation of adult cochlear supporting cells into outer hair cells Sun, Suhong Li, Shuting Luo, Zhengnan Ren, Minhui He, Shunji Wang, Guangqin Liu, Zhiyong eLife Developmental Biology Mammalian cochlear outer hair cells (OHCs) are essential for hearing. Severe hearing impairment follows OHC degeneration. Previous attempts at regenerating new OHCs from cochlear supporting cells (SCs) have been unsuccessful, notably lacking expression of the key OHC motor protein, Prestin. Thus, regeneration of Prestin+ OHCs represents a barrier to restore auditory function in vivo. Here, we reported the successful in vivo conversion of adult mouse cochlear SCs into Prestin+ OHC-like cells through the concurrent induction of two key transcriptional factors known to be necessary for OHC development: Atoh1 and Ikzf2. Single-cell RNA sequencing revealed the upregulation of 729 OHC genes and downregulation of 331 SC genes in OHC-like cells. The resulting differentiation status of these OHC-like cells was much more advanced than previously achieved. This study thus established an efficient approach to induce the regeneration of Prestin+ OHCs, paving the way for in vivo cochlear repair via SC transdifferentiation. eLife Sciences Publications, Ltd 2021-09-03 /pmc/articles/PMC8439656/ /pubmed/34477109 http://dx.doi.org/10.7554/eLife.66547 Text en © 2021, Sun et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Developmental Biology
Sun, Suhong
Li, Shuting
Luo, Zhengnan
Ren, Minhui
He, Shunji
Wang, Guangqin
Liu, Zhiyong
Dual expression of Atoh1 and Ikzf2 promotes transformation of adult cochlear supporting cells into outer hair cells
title Dual expression of Atoh1 and Ikzf2 promotes transformation of adult cochlear supporting cells into outer hair cells
title_full Dual expression of Atoh1 and Ikzf2 promotes transformation of adult cochlear supporting cells into outer hair cells
title_fullStr Dual expression of Atoh1 and Ikzf2 promotes transformation of adult cochlear supporting cells into outer hair cells
title_full_unstemmed Dual expression of Atoh1 and Ikzf2 promotes transformation of adult cochlear supporting cells into outer hair cells
title_short Dual expression of Atoh1 and Ikzf2 promotes transformation of adult cochlear supporting cells into outer hair cells
title_sort dual expression of atoh1 and ikzf2 promotes transformation of adult cochlear supporting cells into outer hair cells
topic Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8439656/
https://www.ncbi.nlm.nih.gov/pubmed/34477109
http://dx.doi.org/10.7554/eLife.66547
work_keys_str_mv AT sunsuhong dualexpressionofatoh1andikzf2promotestransformationofadultcochlearsupportingcellsintoouterhaircells
AT lishuting dualexpressionofatoh1andikzf2promotestransformationofadultcochlearsupportingcellsintoouterhaircells
AT luozhengnan dualexpressionofatoh1andikzf2promotestransformationofadultcochlearsupportingcellsintoouterhaircells
AT renminhui dualexpressionofatoh1andikzf2promotestransformationofadultcochlearsupportingcellsintoouterhaircells
AT heshunji dualexpressionofatoh1andikzf2promotestransformationofadultcochlearsupportingcellsintoouterhaircells
AT wangguangqin dualexpressionofatoh1andikzf2promotestransformationofadultcochlearsupportingcellsintoouterhaircells
AT liuzhiyong dualexpressionofatoh1andikzf2promotestransformationofadultcochlearsupportingcellsintoouterhaircells