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人耳蜗中支持细胞与毛细胞的存活:对再生疗法的启示

Supporting-cell vs. hair-cell survival in the human cochlea: Implications for regenerative therapies.

作者信息

Kaur Charanjeet, Van Orden McKayla, O'Malley Jennifer T, Wu Pei-Zhe, Liberman M Charles

机构信息

Eaton-Peabody Laboratories, Massachusetts Eye and Ear, Boston, MA 02114.

Dept of Otolaryngology-Head & Neck Surgery, Harvard Medical School, Boston, MA 02115.

出版信息

bioRxiv. 2023 Apr 24:2023.04.24.538119. doi: 10.1101/2023.04.24.538119.

Abstract

UNLABELLED

Animal studies have shown that the supporting-cells surviving in the organ of Corti after cochlear insult can be transdifferentiated into hair cells as a treatment for sensorineural hearing loss. Clinical trials of small-molecule therapeutics have been undertaken, but little is known about how to predict the pattern and degree of supporting-cell survival based on audiogram, hearing loss etiology or any other metric obtainable pre-mortem. To address this, we systematically assessed supporting-cell and hair cell survival, as a function of cochlear location in 274 temporal bone cases from the archives at the Massachusetts Eye and Ear and compared the histopathology with the audiograms and hearing-loss etiologies. Results showed that supporting-cell survival was always significantly greater in the apical half than the basal half of the cochlea, that inner pillars were more robust than outer pillars or Deiters' cells, and that total replacement of all supporting cells with a flat epithelium was rare outside of the extreme basal 20% of the cochlea. Supporting cell survival in the basal half of the cochlea was better correlated with the slope of the audiogram than with the mean high-frequency threshold per se: i.e. survival was better with flatter audiograms than with steeply down-sloping audiograms. Cochlear regions with extensive hair cell loss and exceptional supporting cell survival were most common in cases with hearing loss due to ototoxic drugs. Such cases also tended to have less pathology in other functionally critical structures, i.e. spiral ganglion neurons and the stria vascularis.

HIGHLIGHTS

Supporting cell survival was systematically assessed in 274 human cochleasSupporting cell survival was better with flat than with down-sloping audiogramsSupporting cell survival was most robust when hearing loss was from ototoxic drugsOtotoxic cases also showed less pathology in other critical cochlear structuresThe data can inform clinical trials for regeneration via supporting cell conversion.

摘要

未标注

动物研究表明,耳蜗受损后在柯蒂氏器中存活的支持细胞可转分化为毛细胞,作为感音神经性听力损失的一种治疗方法。小分子疗法的临床试验已经开展,但对于如何根据听力图、听力损失病因或生前可获得的任何其他指标来预测支持细胞存活的模式和程度,人们知之甚少。为解决这一问题,我们系统评估了来自马萨诸塞州眼耳医院档案中的274例颞骨病例中,支持细胞和毛细胞的存活情况与耳蜗位置的关系,并将组织病理学与听力图和听力损失病因进行了比较。结果显示,耳蜗顶半部的支持细胞存活总是显著多于基底半部,内柱细胞比外柱细胞或Dieters细胞更具韧性,并且在耳蜗最基部20%以外的区域,很少出现所有支持细胞被扁平上皮完全替代的情况。耳蜗基底半部的支持细胞存活与听力图的斜率比与高频平均阈值本身的相关性更好:即听力图较平坦时的支持细胞存活情况优于急剧下降的听力图。在因耳毒性药物导致听力损失的病例中,毛细胞广泛缺失但支持细胞存活异常的耳蜗区域最为常见。这类病例在其他功能关键结构,即螺旋神经节神经元和血管纹中,病理变化也往往较少。

重点

在274个人类耳蜗中系统评估了支持细胞存活情况

听力图平坦时的支持细胞存活情况优于下降型听力图

听力损失由耳毒性药物导致时,支持细胞存活最具韧性

耳毒性病例在其他关键耳蜗结构中的病理变化也较少

这些数据可为通过支持细胞转化进行再生的临床试验提供参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ce7/10168255/5593d85b6419/nihpp-2023.04.24.538119v1-f0001.jpg

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