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Two Loci Contribute to Age-Related Hearing Loss Resistance in the Japanese Wild-Derived Inbred MSM/Ms Mice
An MSM/Ms strain was established using Japanese wild mice, which exhibit resistance to several phenotypes associated with aging, such as obesity, inflammation, and tumorigenesis, compared to common inbred mouse strains. MSM/Ms strain is resistant to age-related hearing loss, and their auditory abili...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9496148/ https://www.ncbi.nlm.nih.gov/pubmed/36140322 http://dx.doi.org/10.3390/biomedicines10092221 |
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author | Yasuda, Shumpei P. Miyasaka, Yuki Hou, Xuehan Obara, Yo Shitara, Hiroshi Seki, Yuta Matsuoka, Kunie Takahashi, Ai Wakai, Eri Hibino, Hiroshi Takada, Toyoyuki Shiroishi, Toshihiko Kominami, Ryo Kikkawa, Yoshiaki |
author_facet | Yasuda, Shumpei P. Miyasaka, Yuki Hou, Xuehan Obara, Yo Shitara, Hiroshi Seki, Yuta Matsuoka, Kunie Takahashi, Ai Wakai, Eri Hibino, Hiroshi Takada, Toyoyuki Shiroishi, Toshihiko Kominami, Ryo Kikkawa, Yoshiaki |
author_sort | Yasuda, Shumpei P. |
collection | PubMed |
description | An MSM/Ms strain was established using Japanese wild mice, which exhibit resistance to several phenotypes associated with aging, such as obesity, inflammation, and tumorigenesis, compared to common inbred mouse strains. MSM/Ms strain is resistant to age-related hearing loss, and their auditory abilities are sustained for long durations. The age-related hearing loss 3 (ahl3) locus contributes to age-related hearing in MSM/Ms strain. We generated ahl3 congenic strains by transferring a genomic region on chromosome 17 from MSM/Ms mice into C57BL/6J mice. Although C57BL/6J mice develop age-related hearing loss because of the ahl allele of the cadherin 23 gene, the development of middle- to high-frequency hearing loss was significantly delayed in an ahl3 congenic strain. Moreover, the novel age-related hearing loss 10 (ahl10) locus associated with age-related hearing resistance in MSM/Ms strain was mapped to chromosome 12. Although the resistance effects in ahl10 congenic strain were slightly weaker than those in ahl3 congenic strain, slow progression of age-related hearing loss was confirmed in ahl10 congenic strain despite harboring the ahl allele of cadherin 23. These results suggest that causative genes and polymorphisms of the ahl3 and ahl10 loci are important targets for the prevention and treatment of age-related hearing loss. |
format | Online Article Text |
id | pubmed-9496148 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-94961482022-09-23 Two Loci Contribute to Age-Related Hearing Loss Resistance in the Japanese Wild-Derived Inbred MSM/Ms Mice Yasuda, Shumpei P. Miyasaka, Yuki Hou, Xuehan Obara, Yo Shitara, Hiroshi Seki, Yuta Matsuoka, Kunie Takahashi, Ai Wakai, Eri Hibino, Hiroshi Takada, Toyoyuki Shiroishi, Toshihiko Kominami, Ryo Kikkawa, Yoshiaki Biomedicines Article An MSM/Ms strain was established using Japanese wild mice, which exhibit resistance to several phenotypes associated with aging, such as obesity, inflammation, and tumorigenesis, compared to common inbred mouse strains. MSM/Ms strain is resistant to age-related hearing loss, and their auditory abilities are sustained for long durations. The age-related hearing loss 3 (ahl3) locus contributes to age-related hearing in MSM/Ms strain. We generated ahl3 congenic strains by transferring a genomic region on chromosome 17 from MSM/Ms mice into C57BL/6J mice. Although C57BL/6J mice develop age-related hearing loss because of the ahl allele of the cadherin 23 gene, the development of middle- to high-frequency hearing loss was significantly delayed in an ahl3 congenic strain. Moreover, the novel age-related hearing loss 10 (ahl10) locus associated with age-related hearing resistance in MSM/Ms strain was mapped to chromosome 12. Although the resistance effects in ahl10 congenic strain were slightly weaker than those in ahl3 congenic strain, slow progression of age-related hearing loss was confirmed in ahl10 congenic strain despite harboring the ahl allele of cadherin 23. These results suggest that causative genes and polymorphisms of the ahl3 and ahl10 loci are important targets for the prevention and treatment of age-related hearing loss. MDPI 2022-09-07 /pmc/articles/PMC9496148/ /pubmed/36140322 http://dx.doi.org/10.3390/biomedicines10092221 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Yasuda, Shumpei P. Miyasaka, Yuki Hou, Xuehan Obara, Yo Shitara, Hiroshi Seki, Yuta Matsuoka, Kunie Takahashi, Ai Wakai, Eri Hibino, Hiroshi Takada, Toyoyuki Shiroishi, Toshihiko Kominami, Ryo Kikkawa, Yoshiaki Two Loci Contribute to Age-Related Hearing Loss Resistance in the Japanese Wild-Derived Inbred MSM/Ms Mice |
title | Two Loci Contribute to Age-Related Hearing Loss Resistance in the Japanese Wild-Derived Inbred MSM/Ms Mice |
title_full | Two Loci Contribute to Age-Related Hearing Loss Resistance in the Japanese Wild-Derived Inbred MSM/Ms Mice |
title_fullStr | Two Loci Contribute to Age-Related Hearing Loss Resistance in the Japanese Wild-Derived Inbred MSM/Ms Mice |
title_full_unstemmed | Two Loci Contribute to Age-Related Hearing Loss Resistance in the Japanese Wild-Derived Inbred MSM/Ms Mice |
title_short | Two Loci Contribute to Age-Related Hearing Loss Resistance in the Japanese Wild-Derived Inbred MSM/Ms Mice |
title_sort | two loci contribute to age-related hearing loss resistance in the japanese wild-derived inbred msm/ms mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9496148/ https://www.ncbi.nlm.nih.gov/pubmed/36140322 http://dx.doi.org/10.3390/biomedicines10092221 |
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