Generation of four induced pluripotent stem cell lines (KEIUi004-A, KEIUi005-A, KEIUi006-A, and KEIUi007-A) from patients with sensorineural hearing loss with mutation in EYA4 gene
Disease-related cells differentiated from patient-derived iPSCs are useful for elucidating the pathophysiological mechanisms underlying these diseases. In this study, four iPSC lines were established from independent patients with sensorineural hearing loss and a mutation in EYA4. These iPSCs showed...
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Published in | Stem cell research Vol. 79; p. 103489 |
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Main Authors | , , , , , , , , , |
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Elsevier B.V
01.09.2024
Elsevier |
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Abstract | Disease-related cells differentiated from patient-derived iPSCs are useful for elucidating the pathophysiological mechanisms underlying these diseases. In this study, four iPSC lines were established from independent patients with sensorineural hearing loss and a mutation in EYA4. These iPSCs showed pluripotency, the capacity to differentiate into three germ layers, and normal karyotypes, suggesting that these lines are useful for the pathological study of sensorineural hearing loss and drug screening for ear disorders. |
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AbstractList | Disease-related cells differentiated from patient-derived iPSCs are useful for elucidating the pathophysiological mechanisms underlying these diseases. In this study, four iPSC lines were established from independent patients with sensorineural hearing loss and a mutation in EYA4. These iPSCs showed pluripotency, the capacity to differentiate into three germ layers, and normal karyotypes, suggesting that these lines are useful for the pathological study of sensorineural hearing loss and drug screening for ear disorders. Disease-related cells differentiated from patient-derived iPSCs are useful for elucidating the pathophysiological mechanisms underlying these diseases. In this study, four iPSC lines were established from independent patients with sensorineural hearing loss and a mutation in EYA4. These iPSCs showed pluripotency, the capacity to differentiate into three germ layers, and normal karyotypes, suggesting that these lines are useful for the pathological study of sensorineural hearing loss and drug screening for ear disorders.Disease-related cells differentiated from patient-derived iPSCs are useful for elucidating the pathophysiological mechanisms underlying these diseases. In this study, four iPSC lines were established from independent patients with sensorineural hearing loss and a mutation in EYA4. These iPSCs showed pluripotency, the capacity to differentiate into three germ layers, and normal karyotypes, suggesting that these lines are useful for the pathological study of sensorineural hearing loss and drug screening for ear disorders. |
ArticleNumber | 103489 |
Author | Saeki, Tsubasa Mizukoshi, Akifumi Matsuzaki, Saeko Kitajiri, Shin-ichiro Saegusa, Chika Mutai, Hideki Hosoya, Makoto Fujioka, Masato Matsunaga, Tatsuo Okano, Hideyuki |
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References | Okura, Ishii, Suzuki (b0020) 2023; 67 Depreux, Darrow, Conner (b0005) 2008; 118 Hosoya, Fujioka, Sone (b0010) 2017; 18 Okita, Yamakawa, Matsumura (b0015) 2013; 31 Wayne, Robertson, DeClau (b0025) 2001; 10 Hosoya (10.1016/j.scr.2024.103489_b0010) 2017; 18 Wayne (10.1016/j.scr.2024.103489_b0025) 2001; 10 Okita (10.1016/j.scr.2024.103489_b0015) 2013; 31 Depreux (10.1016/j.scr.2024.103489_b0005) 2008; 118 Okura (10.1016/j.scr.2024.103489_b0020) 2023; 67 |
References_xml | – volume: 67 year: 2023 ident: b0020 article-title: Generation of two induced pluripotent stem cell lines from individuals without auditory disorders publication-title: Stem Cell Res. contributor: fullname: Suzuki – volume: 10 start-page: 195 year: 2001 end-page: 200 ident: b0025 article-title: Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus publication-title: Hum. Mol. Genet. contributor: fullname: DeClau – volume: 18 start-page: 68 year: 2017 end-page: 81 ident: b0010 article-title: Cochlear cell modeling using disease-specific iPSCs unveils a degenerative phenotype and suggests treatments for congenital progressive hearing loss publication-title: Cell Rep. contributor: fullname: Sone – volume: 118 start-page: 651 year: 2008 end-page: 658 ident: b0005 article-title: Eya4-deficient mice are a model for heritable otitis media publication-title: J. Clin. Invest. contributor: fullname: Conner – volume: 31 start-page: 458 year: 2013 end-page: 466 ident: b0015 article-title: An efficient nonviral method to generate integration-free human-induced pluripotent stem cells from cord blood and peripheral blood cells publication-title: Stem Cells contributor: fullname: Matsumura – volume: 10 start-page: 195 year: 2001 ident: 10.1016/j.scr.2024.103489_b0025 article-title: Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus publication-title: Hum. Mol. Genet. doi: 10.1093/hmg/10.3.195 contributor: fullname: Wayne – volume: 31 start-page: 458 year: 2013 ident: 10.1016/j.scr.2024.103489_b0015 article-title: An efficient nonviral method to generate integration-free human-induced pluripotent stem cells from cord blood and peripheral blood cells publication-title: Stem Cells doi: 10.1002/stem.1293 contributor: fullname: Okita – volume: 118 start-page: 651 year: 2008 ident: 10.1016/j.scr.2024.103489_b0005 article-title: Eya4-deficient mice are a model for heritable otitis media publication-title: J. Clin. Invest. contributor: fullname: Depreux – volume: 67 year: 2023 ident: 10.1016/j.scr.2024.103489_b0020 article-title: Generation of two induced pluripotent stem cell lines from individuals without auditory disorders publication-title: Stem Cell Res. doi: 10.1016/j.scr.2023.103017 contributor: fullname: Okura – volume: 18 start-page: 68 year: 2017 ident: 10.1016/j.scr.2024.103489_b0010 article-title: Cochlear cell modeling using disease-specific iPSCs unveils a degenerative phenotype and suggests treatments for congenital progressive hearing loss publication-title: Cell Rep. doi: 10.1016/j.celrep.2016.12.020 contributor: fullname: Hosoya |
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SubjectTerms | Cell Differentiation Cell Line Child Female Hearing Loss, Sensorineural - genetics Hearing Loss, Sensorineural - pathology Humans Induced Pluripotent Stem Cells - metabolism Karyotype Male Mutation Trans-Activators - genetics |
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Title | Generation of four induced pluripotent stem cell lines (KEIUi004-A, KEIUi005-A, KEIUi006-A, and KEIUi007-A) from patients with sensorineural hearing loss with mutation in EYA4 gene |
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