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Updated: Dec 26, 2025

Gene Transfer to the Developing Mouse Inner Ear by In Vivo Electroporation
Published on: June 30, 2012
Systemic Fluorescent Gentamicin Enters Neonatal Mouse Hair Cells Predominantly Through Sensory Mechanoelectrical
Ayane Makabe1, Yoshiyuki Kawashima2, Yuriko Sakamaki3
1Department of Otolaryngology, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo, 113-8519, Japan.
Abstract:
Systemically administered aminoglycoside antibiotics can enter inner ear hair cells and trigger apoptosis. However, the in vivo route(s) by which aminoglycoside antibiotics enter hair cells remains controversial. Aminoglycosides can enter mouse hair cells by endocytosis or by permeation through transmembrane ion channels such as sensory mechanoelectrical transduction (MET) channels, transient receptor potential (TRP) channels, P2X channels, Piezo2-containing ion channels, or a combination of these routes. Transmembrane channel-like 1 (TMC1) and TMC2 are essential for sensory MET and appear to be the pore-forming components of sensory MET channels. The present study tested the hypothesis that systemic fluorescent gentamicin enters mouse hair cells predominantly through sensory MET channels. We employed Tmc1Δ, Tmc2Δ, and Tmc1::mCherry mice. In Tmc1::mCherry mice, the transgene was integrated on the X chromosome, resulting in mosaic expression of TMC1-mCherry in the hair cells of female heterozygous mice. After systemic administration of gentamicin-conjugated Texas Red (GTTR) into Tmc1Δ;Tmc2Δ mice and wild-type mice at postnatal day 4 (P4), robust GTTR fluorescence was detected in wild-type hair cells, whereas little or no GTTR fluorescence was detected in Tmc1Δ;Tmc2Δ hair cells. When GTTR was injected into developing mice at P0, P2, P4, or P6, the GTTR fluorescent intensity gradually increased from P0 to P4 in wild-type hair cells, whereas the intensity was stably low from P0 through P6 in Tmc1Δ;Tmc2Δ hair cells. The increase in the GTTR intensity coincided with the spatio-temporal onset of sensory MET in wild-type hair cells. In Tmc1::mCherry cochleae, only hair cells that showed a significant uptake of systemic GTTR took up FM1-43. Transmission electron microscopy could detect no disruption of normal endocytosis at the apical surface of Tmc1Δ;Tmc2Δ hair cells in vitro. These results provide substantial novel evidence that in vivo gentamicin enters neonatal mouse hair cells predominantly through sensory MET channels and not via endocytosis.
Insights
Systemic gentamicin enters neonatal mouse inner ear hair cells primarily through sensory mechanoelectrical transduction (MET) channels, not endocytosis. This finding clarifies the ototoxicity pathway for aminoglycoside antibiotics.
Area of Science:
- Ototoxicity and auditory neuroscience
- Cellular biology and ion channel function
- Pharmacology of antibiotic entry into inner ear cells
Background:
- Aminoglycoside antibiotics can cause inner ear hair cell apoptosis.
- The precise in vivo entry route of aminoglycosides into hair cells is debated.
- Potential entry routes include endocytosis and ion channels like MET, TRP, P2X, and Piezo2.
Purpose of the Study:
- To test the hypothesis that systemic gentamicin enters mouse hair cells predominantly via sensory mechanoelectrical transduction (MET) channels.
- To elucidate the primary in vivo pathway for aminoglycoside antibiotic entry into developing hair cells.
Main Methods:
- Utilized Tmc1Δ, Tmc2Δ, and Tmc1::mCherry genetically modified mice.
- Administered fluorescent gentamicin-conjugated Texas Red (GTTR) systemically at various neonatal stages (P0-P6).
- Analyzed GTTR fluorescence in hair cells using microscopy and correlated with sensory MET onset and FM1-43 uptake; performed transmission electron microscopy.
Main Results:
- Robust GTTR fluorescence observed in wild-type hair cells, but minimal in Tmc1Δ;Tmc2Δ hair cells after systemic GTTR administration.
- GTTR uptake increased with age in wild-type hair cells, coinciding with sensory MET onset, while remaining low in Tmc1Δ;Tmc2Δ mice.
- Hair cells showing GTTR uptake also took up FM1-43; no endocytosis disruption was observed in Tmc1Δ;Tmc2Δ hair cells.
Conclusions:
- Systemic gentamicin enters neonatal mouse hair cells predominantly through sensory MET channels.
- Endocytosis is not the primary route for gentamicin entry into these cells in vivo.
- Transmembrane channel-like 1 (TMC1) and TMC2 are critical for aminoglycoside entry via sensory MET channels.

