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 inStem cell research Vol. 79; p. 103489
Main Authors Saegusa, Chika, Mutai, Hideki, Saeki, Tsubasa, Matsuzaki, Saeko, Mizukoshi, Akifumi, Kitajiri, Shin-ichiro, Matsunaga, Tatsuo, Hosoya, Makoto, Okano, Hideyuki, Fujioka, Masato
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Published England 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.
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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10.1002/stem.1293
10.1016/j.scr.2023.103017
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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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Snippet Disease-related cells differentiated from patient-derived iPSCs are useful for elucidating the pathophysiological mechanisms underlying these diseases. In this...
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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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