In mammals, the permanence of many forms of hearing loss is the result of the inner ear's inability to replace lost sensory hair cells. Here, we apply a differentiation strategy to guide human embryonic stem cells (hESCs) into cells of the otic lineage using chemically defined attached-substrate conditions. The generation of human otic progenitor cells was dependent on fibroblast growth factor (FGF) signaling, and protracted culture led to the upregulation of markers indicative of differentiated inner ear sensory epithelia. Using a transgenic ESC reporter line based on a murine Atoh1 enhancer, we show that differentiated hair cell-like cells express multiple hair cell markers simultaneously. Hair cell-like cells displayed protrusions reminiscent of stereociliary bundles, but failed to fully mature into cells with typical hair cell cytoarchitecture. We conclude that optimized defined conditions can be used in vitro to attain otic progenitor specification and sensory cell differentiation.
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http://dx.doi.org/10.1089/scd.2014.0033 | DOI Listing |
Mol Genet Genomic Med
December 2024
Department of Otolaryngology-Head and Neck Surgery, Lanzhou University Second Hospital, Lanzhou, Gansu, China.
Aging (Albany NY)
October 2024
Department of Otolaryngology, The First People’s Hospital of Changzhou, Jiangsu 213003, China.
Age-related hearing loss (AHL) is a prevalent and multifaceted condition that significantly impacts a substantial portion of the aging population. Oxysterol Binding Protein-like 2 (OSBPL2) has been identified as a causal gene for hearing loss. However, its role in AHL is still unclear.
View Article and Find Full Text PDFPNAS Nexus
October 2024
Department of Neuroscience, Baylor College of Medicine, Houston, TX 77030, USA.
Development
November 2024
Department of Cell and Molecular Biology, Karolinska Institutet, Stockholm 17177, Sweden.
Notch signaling patterns the cochlear organ of Corti, and individuals with the JAG1/NOTCH2-related genetic disorder Alagille syndrome can thus experience hearing loss. We investigated the function of Jag1 in cochlear patterning and signaling using Jag1Ndr/Ndr mice, which are a model of Alagille syndrome. Jag1Ndr/Ndr mice exhibited expected vestibular and auditory deficits, a dose-dependent increase in ectopic inner hair cells, and a reduction in outer hair cells.
View Article and Find Full Text PDFExp Cell Res
June 2024
Department of Otorhinolaryngology-Head and Neck Surgery, Nantong University Wuxi Clinical College Affiliated Wuxi No.2 People's Hospital, Wuxi, Jiangsu, China.
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