Mitochondrial alterations in the cochlea of Cdk5rap1‐knockout mice with age‐related hearing loss

Author:

Miwa Toru12ORCID,Katsuno Tatsuya2,Wei Fan‐Yan34ORCID,Tomizawa Kazuhito3ORCID

Affiliation:

1. Department of Otolaryngology‐Head and Neck Surgery, Graduate School of Medicine Kyoto University Japan

2. Department of Otolaryngology‐Head and Neck Surgery Osaka Metropolitan University Japan

3. Department of Molecular Physiology, Faculty of Life Sciences Kumamoto University Japan

4. Department of Modomics Biology and Medicine, Institute of Development, Aging and Cancer Tohoku University Sendai Japan

Abstract

Previous studies have revealed that age‐related hearing loss (AHL) in Cdk5 regulatory subunit‐associated protein 1 (Cdk5rap1)‐knockout mice is associated with pathology in the cochlea. Here, we aimed to identify mitochondrial alterations in the cochlea of Cdk5rap1‐knockout mice with AHL. Mitochondria in the spiral ganglion neurons (SGNs) and hair cells (HCs) were normal despite senescence; however, the mitochondria of types I, II, and IV spiral ligament fibrocytes were ballooned, damaged, and ballooned, respectively, in the stria vascularis. Our results suggest that the accumulation of dysfunctional mitochondria in the lateral wall, rather than the loss of HCs and SGNs, leads to the onset of AHL. Our results provide valuable information regarding the underlying mechanisms of AHL and the relationship between aberrant tRNA modification‐induced hearing loss and mitochondrial dysfunction.

Publisher

Wiley

Subject

General Biochemistry, Genetics and Molecular Biology

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