The cochlea is built to last a lifetime

被引:4
|
作者
Savas, Jeffrey N. [1 ]
机构
[1] Northwestern Univ, Feinberg Sch Med, Dept Neurol, Chicago, IL 60611 USA
基金
美国国家卫生研究院;
关键词
Long-lived proteins; Proteostasis; Protein degradation; Proteasome; Ubiquitin; Autophagy; Lysosome; Noise induced hearing loss; Post -mitotic cells; INDUCED HEARING-LOSS; INNER-EAR; TECTORIAL MEMBRANE; BASILAR-MEMBRANE; CELL-DEATH; PROTEIN; DAMAGE; NOISE; DEGENERATION; RACEMIZATION;
D O I
10.1016/j.heares.2023.108821
中图分类号
R36 [病理学]; R76 [耳鼻咽喉科学];
学科分类号
100104 ; 100213 ;
摘要
Orchestration of protein production and degradation and the regulation of protein lifetimes play a cen-tral role in many basic biological processes. Nearly all mammalian proteins are replenished by protein turnover in waves of synthesis and degradation. Protein lifetimes in vivo are typically measured in days, but a small number of extremely long-lived proteins (ELLPs) persist for months or even years. ELLPs are rare in all tissues but are enriched in tissues containing terminally differentiated post-mitotic cells and extracellular matrix. Consistently, emerging evidence suggests that the cochlea may be particularly en-riched in ELLPs. Damage to ELLPs in specialized cell types, such as crystallin in the lens cells of the eye, causes organ failure such as cataracts. Similarly, damage to cochlear ELLPs is likely to occur with many insults, including acoustic overstimulation, drugs, anoxia, and antibiotics, and may play an underappreci-ated role in hearing loss. Furthermore, hampered protein degradation may contribute to acquired hearing loss. In this review, I highlight our knowledge of the lifetimes of cochlear proteins with an emphasis on ELLPs and the potential contribution that impaired cochlear protein degradation has on acquired hearing loss and the emerging relevance of ELLPs.& COPY; 2023 The Author. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license ( http://creativecommons.org/licenses/by-nc-nd/4.0/ )
引用
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页数:7
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