4.7 Article

Nox3-Derived Superoxide in Cochleae Induces Sensorineural Hearing Loss

Journal

JOURNAL OF NEUROSCIENCE
Volume 41, Issue 21, Pages 4716-4731

Publisher

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.2672-20.2021

Keywords

age-related hearing loss; drug-induced hearing loss; hearing loss; NADPH oxidase; noise-induced hearing loss; reactive oxygen species

Categories

Funding

  1. Japan Society for the Promotion of Sciences Kakenhi Grants [JP19K22472, JP21H02672, JP18K09383]
  2. Japan Agency for Medical Research and Development [JP19ek0109398]
  3. Hyogo Science and Technology Association [30075]
  4. Naito Foundation
  5. Japan Foundation for Applied Enzymology
  6. Terumo Life Science Foundation
  7. joint research program of the Biosignal Research Center, Kobe University [301004, 192003]

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Research has shown that the expression of Nox3 in the inner ear is associated with sensorineural hearing loss (SNHL), particularly playing a significant role in cisplatin-induced hearing loss, age-related hearing loss, and noise-induced hearing loss. This suggests that inhibiting Nox3 in the cochlea may be a promising strategy for treating ROS-related SNHL.
Reactive oxygen species (ROS) produced by NADPH oxidases (Nox) contribute to the development of different types of sensorineural hearing loss (SNHL), a common impairment in humans with no established treatment. Although the essential role of Nox3 in otoconia biosynthesis and its possible involvement in hearing have been reported in rodents, immunohistological methods targeted at detecting Nox3 expression in inner ear cells reveal ambiguous results. Therefore, the mechanism underlying Nox3-dependent SNHL remains unclear and warrants further investigation. We generated Nox3-Cre knock-in mice, in which Nox3 was replaced with Cre recombinase (Cre). Using Nox3-Cre;tdTomato mice of either sex, in which tdTomato is expressed under the control of the Nox3 promoter, we determined Nox3-expressing regions and cell types in the inner ear. Nox3-expressing cells in the cochlea included various types of supporting cells, outer hair cells, inner hair cells, and spiral ganglion neurons. Nox3 expression increased with cisplatin, age, and noise insults. Moreover, increased Nox3 expression in supporting cells and outer hair cells, especially at the basal turn of the cochlea, played essential roles in ROS-related SNHL. The extent of Nox3 involvement in SNHL follows the following order: cisplatin-induced hearing loss. age-related hearing loss. noise-induced hearing loss. Here, on the basis of Nox3-Cre;tdTomato, which can be used as a reporter system (Nox3-Cre(+/-);tdTomato(+/+) and Nox3-Cre(+/+);tdTomato(+/+)), and Nox3-KO (Nox3-Cre(+/+);tdTomato(+/+)) mice, we demonstrate that Nox3 inhibition in the cochlea is a promising strategy for ROS-related SNHL, such as cisplatin-induced HL, age-related HL, and noise-induced HL.

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