» Articles » PMID: 35250483

Hearing Recovery Induced by DNA Demethylation in a Chemically Deafened Adult Mouse Model

Overview
Specialty Cell Biology
Date 2022 Mar 7
PMID 35250483
Authors
Affiliations
Soon will be listed here.
Abstract

Functional hair cell regeneration in the adult mammalian inner ear remains challenging. This study aimed to study the function of new hair cells induced by a DNA demethylating agent 5-azacytidine. Adult mice were deafened chemically, followed by injection of 5-azacytidine or vehicle into the inner ear. Functionality of regenerated hair cells was evaluated by expression of hair cell proteins, auditory brainstem response (ABR), and distortion-product otoacoustic emission (DPOAE) tests for 6 weeks. In the vehicle-treated group, no cells expressed the hair cell-specific protein myosin VIIa in the cochlea, whereas numerous myosin VIIa-expressing cells were found in the 5-azacytidine-treated cochlea, suggesting the regeneration of auditory hair cells. Moreover, regenerated hair cells were co-labeled with functional proteins espin and prestin. Expression of ribbon synapse proteins suggested synapse formation between new hair cells and neurons. In hearing tests, progressive improvements in ABR [5-30 dB sound pressure level (SPL)] and DPOAE (5-20 dB) thresholds were observed in 5-azacytidine-treated mice. In vehicle-treated mice, there were <5 dB threshold changes in hearing tests. This study demonstrated the ability of 5-azacytidine to promote the functional regeneration of auditory hair cells in a mature mouse model DNA demethylation, which may provide insights into hearing regeneration using an epigenetic approach.

Citing Articles

Exploring the application of stem cell technology in treating sensorineural hearing loss.

Li M, Ma R, Li Q, Guo M Am J Stem Cells. 2024; 13(4):212-221.

PMID: 39308766 PMC: 11411250. DOI: 10.62347/AEIV5813.


Long-term survival of LGR5 expressing supporting cells after severe ototoxic trauma in the adult mouse cochlea.

Smith-Cortinez N, Hendriksen F, Ramekers D, Stokroos R, Versnel H, Straatman L Front Cell Neurosci. 2023; 17:1236894.

PMID: 37692553 PMC: 10483136. DOI: 10.3389/fncel.2023.1236894.


Advancements in inner ear development, regeneration, and repair through otic organoids.

Nist-Lund C, Kim J, Koehler K Curr Opin Genet Dev. 2022; 76:101954.

PMID: 35853286 PMC: 10425989. DOI: 10.1016/j.gde.2022.101954.

References
1.
Parham K, Sun X, Kim D . Distortion product otoacoustic emissions in the CBA/J mouse model of presbycusis. Hear Res. 1999; 134(1-2):29-38. DOI: 10.1016/s0378-5955(99)00059-3. View

2.
Chen Y, Gu Y, Li Y, Li G, Chai R, Li W . Generation of mature and functional hair cells by co-expression of Gfi1, Pou4f3, and Atoh1 in the postnatal mouse cochlea. Cell Rep. 2021; 35(3):109016. DOI: 10.1016/j.celrep.2021.109016. View

3.
Dallos P . Cochlear amplification, outer hair cells and prestin. Curr Opin Neurobiol. 2008; 18(4):370-6. PMC: 2630119. DOI: 10.1016/j.conb.2008.08.016. View

4.
Hu Z, Komal F, Singh A, Deng M . Generation of a Spiral Ganglion Neuron Degeneration Mouse Model. Front Cell Dev Biol. 2021; 9:761847. PMC: 8578993. DOI: 10.3389/fcell.2021.761847. View

5.
HAWKINS Jr J, Johnsson L, Stebbins W, Moody D, Coombs S . Hearing loss and cochlear pathology in monkeys after noise exposure. Acta Otolaryngol. 1976; 81(3-4):337-43. DOI: 10.3109/00016487609119971. View