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The role of Espin in the stereocilia regeneration and protection in Atoh1‐overexpressed cochlear epithelium
Hair cells (HCs) in mammals cannot spontaneously regenerate after damage. Atoh1 overexpression can promote HC regeneration in the postnatal cochlea, but the regenerated HCs do not possess the structural and functional characteristics of HCs in situ. The stereocilia on the apical surface of HCs are t...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10623949/ https://www.ncbi.nlm.nih.gov/pubmed/37084708 http://dx.doi.org/10.1111/cpr.13483 |
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author | Yang, Xuechun Qi, Jieyu Zhang, Liyan Tan, Fangzhi Huang, Hongming Xu, Chunlai Cui, Yong Chai, Renjie Wu, Peina |
author_facet | Yang, Xuechun Qi, Jieyu Zhang, Liyan Tan, Fangzhi Huang, Hongming Xu, Chunlai Cui, Yong Chai, Renjie Wu, Peina |
author_sort | Yang, Xuechun |
collection | PubMed |
description | Hair cells (HCs) in mammals cannot spontaneously regenerate after damage. Atoh1 overexpression can promote HC regeneration in the postnatal cochlea, but the regenerated HCs do not possess the structural and functional characteristics of HCs in situ. The stereocilia on the apical surface of HCs are the first‐level structure for sound conduction, and regeneration of functional stereocilia is the key basis for the reproduction of functional HCs. Espin, as an actin bundling protein, plays an important role in the development and structural maintenance of the stereocilia. Here, we found that the upregulation of Espin by AAV‐ie was able to induced the aggregation of actin fibres in Atoh1‐induced HCs in both cochlear organoids and explants. In addition, we found that persistent Atoh1 overexpression resulted in impaired stereocilia in both endogenous and newly formed HCs. In contrast, the forced expression of Espin in endogenous and regenerative HCs was able to eliminate the stereocilia damage caused by persistent Atoh1 overexpression. Our study shows that the enhanced expression of Espin can optimize the developmental process of stereocilia in Atoh1‐induced HCs and can attenuate the damage to native HCs induced by Atoh1 overexpression. These results suggest an effective method to induce the maturation of stereocilia in regenerative HCs and pave the way for functional HC regeneration via supporting cell transdifferentiation. |
format | Online Article Text |
id | pubmed-10623949 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-106239492023-11-04 The role of Espin in the stereocilia regeneration and protection in Atoh1‐overexpressed cochlear epithelium Yang, Xuechun Qi, Jieyu Zhang, Liyan Tan, Fangzhi Huang, Hongming Xu, Chunlai Cui, Yong Chai, Renjie Wu, Peina Cell Prolif Original Articles Hair cells (HCs) in mammals cannot spontaneously regenerate after damage. Atoh1 overexpression can promote HC regeneration in the postnatal cochlea, but the regenerated HCs do not possess the structural and functional characteristics of HCs in situ. The stereocilia on the apical surface of HCs are the first‐level structure for sound conduction, and regeneration of functional stereocilia is the key basis for the reproduction of functional HCs. Espin, as an actin bundling protein, plays an important role in the development and structural maintenance of the stereocilia. Here, we found that the upregulation of Espin by AAV‐ie was able to induced the aggregation of actin fibres in Atoh1‐induced HCs in both cochlear organoids and explants. In addition, we found that persistent Atoh1 overexpression resulted in impaired stereocilia in both endogenous and newly formed HCs. In contrast, the forced expression of Espin in endogenous and regenerative HCs was able to eliminate the stereocilia damage caused by persistent Atoh1 overexpression. Our study shows that the enhanced expression of Espin can optimize the developmental process of stereocilia in Atoh1‐induced HCs and can attenuate the damage to native HCs induced by Atoh1 overexpression. These results suggest an effective method to induce the maturation of stereocilia in regenerative HCs and pave the way for functional HC regeneration via supporting cell transdifferentiation. John Wiley and Sons Inc. 2023-04-21 /pmc/articles/PMC10623949/ /pubmed/37084708 http://dx.doi.org/10.1111/cpr.13483 Text en © 2023 The Authors. Cell Proliferation published by Beijing Institute for Stem Cell and Regenerative Medicine and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Yang, Xuechun Qi, Jieyu Zhang, Liyan Tan, Fangzhi Huang, Hongming Xu, Chunlai Cui, Yong Chai, Renjie Wu, Peina The role of Espin in the stereocilia regeneration and protection in Atoh1‐overexpressed cochlear epithelium |
title | The role of Espin in the stereocilia regeneration and protection in Atoh1‐overexpressed cochlear epithelium |
title_full | The role of Espin in the stereocilia regeneration and protection in Atoh1‐overexpressed cochlear epithelium |
title_fullStr | The role of Espin in the stereocilia regeneration and protection in Atoh1‐overexpressed cochlear epithelium |
title_full_unstemmed | The role of Espin in the stereocilia regeneration and protection in Atoh1‐overexpressed cochlear epithelium |
title_short | The role of Espin in the stereocilia regeneration and protection in Atoh1‐overexpressed cochlear epithelium |
title_sort | role of espin in the stereocilia regeneration and protection in atoh1‐overexpressed cochlear epithelium |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10623949/ https://www.ncbi.nlm.nih.gov/pubmed/37084708 http://dx.doi.org/10.1111/cpr.13483 |
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