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Updated: Apr 20, 2026

Initiating Differentiation in Immortalized Multipotent Otic Progenitor Cells
Published on: January 2, 2016
Generation of human induced pluripotent stem cell lines from a patient with OTOF-related deafness and a carrier
Meirong Yu1, Yangyiyi Huang2, Pengfang Lin2
1Center for Basic and Translational Research, the Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Abstract:
OTOF-related deafness (DFNB9) is an auditory neuropathy caused by mutations in the OTOF gene, disrupting synaptic transmission in the inner ear. We generated two human induced pluripotent stem cell (iPSC) lines using transgene-free episomal reprogramming: ZEENTi001-A from a patient with compound heterozygous OTOF mutations (c.2122C > T and c.5197G > A) and ZEENTi002-A from a heterozygous carrier. Both lines demonstrated normal pluripotency, karyotype, and trilineage differentiation, serving as critical tools for mechanistic studies, gene therapy optimization, and drug screening in DFNB9. ZEENTi002-A further enables comparative analyses to elucidate heterozygous mutation effects in auditory pathology.
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