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Transgenic Tmc2 expression preserves inner ear hair cells and vestibular function in mice lacking Tmc1
Recent work has demonstrated that transmembrane channel-like 1 protein (TMC1) is an essential component of the sensory transduction complex in hair cells of the inner ear. A closely related homolog, TMC2, is expressed transiently in the neonatal mouse cochlea and can enable sensory transduction in T...
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Published in: | Scientific reports 2018-08, Vol.8 (1), p.12124-15, Article 12124 |
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Main Authors: | , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Recent work has demonstrated that transmembrane channel-like 1 protein (TMC1) is an essential component of the sensory transduction complex in hair cells of the inner ear. A closely related homolog, TMC2, is expressed transiently in the neonatal mouse cochlea and can enable sensory transduction in
Tmc1
-null mice during the first postnatal week. Both TMC1 and TMC2 are expressed at adult stages in mouse vestibular hair cells. The extent to which TMC1 and TMC2 can substitute for each other is unknown. Several biophysical differences between TMC1 and TMC2 suggest these proteins perform similar but not identical functions. To investigate these differences, and whether TMC2 can substitute for TMC1 in mature hair cells, we generated a knock-in mouse model allowing
Cre
-inducible expression of
Tmc2
. We assayed for changes in hair cell sensory transduction and auditory and vestibular function in
Tmc2
knockin mice (
Tm
[
Tmc2
]) in the presence or absence of endogenous
Tmc1
,
Tmc2
or both. Our results show that expression of Tm[TMC2] restores sensory transduction in vestibular hair cells and transiently in cochlear hair cells in the absence of TMC1. The cellular rescue leads to recovery of balance but not auditory function. We conclude that TMC1 provides some additional necessary function, not provided by TMC2. |
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ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/s41598-018-28958-x |