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Genetic Correction of Induced Pluripotent Stem Cells From a Deaf Patient With MYO7A Mutation Results in Morphologic and Functional Recovery of the Derived Hair Cell-Like Cells.
- Source :
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Stem cells translational medicine [Stem Cells Transl Med] 2016 May; Vol. 5 (5), pp. 561-71. Date of Electronic Publication: 2016 Mar 24. - Publication Year :
- 2016
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Abstract
- Unlabelled: The genetic correction of induced pluripotent stem cells (iPSCs) induced from somatic cells of patients with sensorineural hearing loss (caused by hereditary factors) is a promising method for its treatment. The correction of gene mutations in iPSCs could restore the normal function of cells and provide a rich source of cells for transplantation. In the present study, iPSCs were generated from a deaf patient with compound heterozygous MYO7A mutations (c.1184G>A and c.4118C>T; P-iPSCs), the asymptomatic father of the patient (MYO7A c.1184G>A mutation; CF-iPSCs), and a normal donor (MYO7A(WT/WT); C-iPSCs). One of MYO7A mutation sites (c.4118C>T) in the P-iPSCs was corrected using CRISPR/Cas9. The corrected iPSCs (CP-iPSCs) retained cell pluripotency and normal karyotypes. Hair cell-like cells induced from CP-iPSCs showed restored organization of stereocilia-like protrusions; moreover, the electrophysiological function of these cells was similar to that of cells induced from C-iPSCs and CF-iPSCs. These results might facilitate the development of iPSC-based gene therapy for genetic disorders.<br />Significance: Induced pluripotent stem cells (iPSCs) were generated from a deaf patient with compound heterozygous MYO7A mutations (c.1184G>A and c.4118C>T). One of the MYO7A mutation sites (c.4118C>T) in the iPSCs was corrected using CRISPR/Cas9. The genetic correction of MYO7A mutation resulted in morphologic and functional recovery of hair cell-like cells derived from iPSCs. These findings confirm the hypothesis that MYO7A plays an important role in the assembly of stereocilia into stereociliary bundles. Thus, the present study might provide further insight into the pathogenesis of sensorineural hearing loss and facilitate the development of therapeutic strategies against monogenic disease through the genetic repair of patient-specific iPSCs.<br /> (©AlphaMed Press.)
- Subjects :
- Cell Differentiation
Cell Line
DNA Mutational Analysis
Female
Gene Expression Regulation
Genetic Predisposition to Disease
Hearing Loss, Sensorineural diagnosis
Hearing Loss, Sensorineural pathology
Hearing Loss, Sensorineural surgery
Heredity
Heterozygote
Humans
Male
Membrane Potentials
Myosin VIIa
Pedigree
Phenotype
Recovery of Function
Transfection
CRISPR-Cas Systems
Cell Shape
Hair Cells, Auditory metabolism
Hair Cells, Auditory transplantation
Hair Cells, Auditory ultrastructure
Hearing Loss, Sensorineural genetics
Induced Pluripotent Stem Cells metabolism
Induced Pluripotent Stem Cells transplantation
Induced Pluripotent Stem Cells ultrastructure
Mutation
Myosins genetics
Targeted Gene Repair methods
Subjects
Details
- Language :
- English
- ISSN :
- 2157-6564
- Volume :
- 5
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Stem cells translational medicine
- Publication Type :
- Academic Journal
- Accession number :
- 27013738
- Full Text :
- https://doi.org/10.5966/sctm.2015-0252