International Cancer Center, Marshall Laboratory of Biomedical Engineering, Department of Otolaryngology, The First Affiliated Hospital, Department of Anatomy and Histology, Shenzhen University Medical School, Shenzhen 518060, China.
Department of Pathology, Shenzhen University Medical School, Shenzhen 518060, China.
J Neurosci. 2024 Oct 16;44(42):e0132242024. doi: 10.1523/JNEUROSCI.0132-24.2024.
Cochlear hair cells (HCs) sense sound waves and allow us to hear. Loss of HCs will cause irreversible sensorineural hearing loss. It is well known that DNA damage repair plays a critical role in protecting cells in many organs. However, how HCs respond to DNA damage and how defective DNA damage repair contributes to hearing loss remain elusive. In this study, we showed that cisplatin induced DNA damage in outer hair cells (OHCs) and promoted OHC loss, leading to hearing loss in mice of either sex. Cisplatin induced the expression of Brca1, a DNA damage repair factor, in OHCs. Deficiency of Brca1 induced OHC and hearing loss, and further promoted cisplatin-induced DNA damage in OHCs, accelerating OHC loss. This study provides the first in vivo evidence demonstrating that cisplatin mainly induces DNA damage in OHCs and that BRCA1 promotes repair of DNA damage in OHCs and prevents hearing loss. Our findings not only demonstrate that DNA damage-inducing agent generates DNA damage in postmitotic HCs but also suggest that DNA repair factors, like BRCA1, protect postmitotic HCs from DNA damage-induced cell death and hearing loss.
耳蜗毛细胞 (HCs) 感知声波,使我们能够听到声音。 HCs 的损失会导致不可逆转的感音神经性听力损失。众所周知,DNA 损伤修复在保护许多器官中的细胞方面起着至关重要的作用。然而,HCs 如何对 DNA 损伤做出反应,以及有缺陷的 DNA 损伤修复如何导致听力损失,仍然难以捉摸。在这项研究中,我们表明顺铂诱导外毛细胞 (OHCs) 中的 DNA 损伤,并促进 OHC 损失,导致雌雄小鼠听力损失。顺铂诱导了 OHC 中 DNA 损伤修复因子 Brca1 的表达。Brca1 的缺失导致 OHC 和听力损失,并进一步促进了 OHC 中的顺铂诱导的 DNA 损伤,加速了 OHC 的损失。这项研究提供了第一个体内证据,证明顺铂主要诱导 OHC 中的 DNA 损伤,而 BRCA1 促进 OHC 中的 DNA 损伤修复,并防止听力损失。我们的研究结果不仅表明有丝分裂后 HCs 中的致 DNA 损伤剂会产生 DNA 损伤,而且表明 DNA 修复因子(如 BRCA1)可保护有丝分裂后 HCs 免受 DNA 损伤诱导的细胞死亡和听力损失。