Rescue of Outer Hair Cells with Antisense Oligonucleotides in Usher Mice Is Dependent on Age of Treatment
Open Access
- 12 October 2017
- journal article
- research article
- Published by Springer Nature in Journal of the Association for Research in Otolaryngology
- Vol. 19 (1) , 1-16
Abstract
The absence of functional outer hair cells is a component of several forms of hereditary hearing impairment, including Usher syndrome, the most common cause of concurrent hearing and vision loss. Antisense oligonucleotide (ASO) treatment of mice with the human Usher mutation, Ush1c c.216G>A, corrects gene expression and significantly improves hearing, as measured by auditory-evoked brainstem responses (ABRs), as well as inner and outer hair cell (IHC and OHC) bundle morphology. However, it is not clear whether the improvement in hearing achieved by ASO treatment involves the functional rescue of outer hair cells. Here, we show that Ush1c c.216AA mice lack OHC function as evidenced by the absence of distortion product otoacoustic emissions (DPOAEs) in response to low-, mid-, and high-frequency tone pairs. This OHC deficit is rescued by treatment with an ASO that corrects expression of Ush1c c.216G>A. Interestingly, although rescue of inner hairs cells, as measured by ABR, is achieved by ASO treatment as late as 7 days after birth, rescue of outer hair cells, measured by DPOAE, requires treatment before post-natal day 5. These results suggest that ASO-mediated rescue of both IHC and OHC function is age dependent and that the treatment window is different for the different cell types. The timing of treatment for congenital hearing disorders is of critical importance for the development of drugs such ASO-29 for hearing rescue.Keywords
Funding Information
- National Institute on Deafness and Other Communication Disorders (1R01DC012596)
- National Institute of General Medical Sciences (1 U54 GM104940)
- National Institutes of Health (P30 GM104940)
- Foundation Fighting Blindness (TA-NMT-0613-0609-LSU-WG)
- Eye on Jacob Foundation
- Ush One See Foundation
- Usher 2020 Foundation
- Hearing Health Foundation
- Midwest Eye-Banks
- Capita Foundation
- National Organization for Hearing Research Foundation
This publication has 53 references indexed in Scilit:
- Rescue of hearing and vestibular function by antisense oligonucleotides in a mouse model of human deafnessNature Medicine, 2013
- Over Half the Hair Cells in the Mouse Utricle First Appear After Birth, with Significant Numbers Originating from Early Postnatal Mitotic Production in Peripheral and Striolar Growth ZonesJournal of the Association for Research in Otolaryngology, 2012
- Eya1-Six1 Interaction Is Sufficient to Induce Hair Cell Fate in the Cochlea by Activating Atoh1 Expression in Cooperation with Sox2Developmental Cell, 2012
- Deafness and retinal degeneration in a novel USH1C knock‐in mouse modelDevelopmental Neurobiology, 2010
- Harmonin Mutations Cause Mechanotransduction Defects in Cochlear Hair CellsNeuron, 2009
- Evolutionary insights into the unique electromotility motor of mammalian outer hair cellsEvolution & Development, 2008
- Prestin-Based Outer Hair Cell Motility Is Necessary for Mammalian Cochlear AmplificationNeuron, 2008
- Ush1c216A knock-in mouse survives KatrinaMutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 2007
- Hearing thresholds with outer and inner hair cell lossAmerican Journal of Otolaryngology, 1979
- Effect of absence of cochlear outer hair cells on behavioural auditory thresholdNature, 1975