Taura A, Taura K, Koyama Y, Yamamoto N, Nakagawa T, Ito J, Ryan A F
Department of Otolaryngology-Head and Neck Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Department of Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Gene Ther. 2016 May;23(5):415-23. doi: 10.1038/gt.2016.12. Epub 2016 Mar 10.
Once inner ear hair cells (HCs) are damaged by drugs, noise or aging, their apical structures including the stereociliary arrays are frequently the first cellular feature to be lost. Although this can be followed by progressive loss of HC somata, a significant number of HC bodies often remain even after stereociliary loss. However, in the absence of stereocilia they are nonfunctional. HCs can sometimes be regenerated by Atoh1 transduction or Notch inhibition, but they also may lack stereociliary bundles. It is therefore important to develop methods for the regeneration of stereocilia, in order to achieve HC functional recovery. Espin is an actin-bundling protein known to participate in sterociliary elongation during development. We evaluated stereociliary array regeneration in damaged vestibular sensory epithelia in tissue culture, using viral vector transduction of two espin isoforms. Utricular HCs were damaged with aminoglycosides. The utricles were then treated with a γ-secretase inhibitor, followed by espin or control transduction and histochemistry. Although γ-secretase inhibition increased the number of HCs, few had stereociliary arrays. In contrast, 46 h after espin1 transduction, a significant increase in hair-bundle-like structures was observed. These were confirmed to be immature stereociliary arrays by scanning electron microscopy. Increased uptake of FM1-43 uptake provided evidence of stereociliary function. Espin4 transduction had no effect. The results demonstrate that espin1 gene therapy can restore stereocilia on damaged or regenerated HCs.
一旦内耳毛细胞(HCs)因药物、噪音或衰老而受损,其包括静纤毛束在内的顶端结构往往是最先丧失的细胞特征。尽管随后可能会出现HC胞体的逐渐丧失,但即使在静纤毛丧失后,仍有相当数量的HC胞体常常留存。然而,在没有静纤毛的情况下,它们是无功能的。HCs有时可通过Atoh1转导或Notch抑制实现再生,但它们也可能缺乏静纤毛束。因此,开发静纤毛再生方法以实现HC功能恢复很重要。Espin是一种肌动蛋白成束蛋白,已知在发育过程中参与静纤毛伸长。我们使用两种Espin亚型的病毒载体转导,在组织培养中评估受损前庭感觉上皮中的静纤毛束再生情况。椭圆囊HCs用氨基糖苷类药物损伤。然后用γ-分泌酶抑制剂处理椭圆囊,接着进行Espin或对照转导及组织化学分析。尽管γ-分泌酶抑制增加了HCs的数量,但很少有静纤毛束。相比之下,在Espin1转导后46小时,观察到类似毛束的结构显著增加。通过扫描电子显微镜证实这些是不成熟的静纤毛束。FM1-43摄取增加提供了静纤毛功能的证据。Espin4转导没有效果。结果表明,Espin1基因治疗可恢复受损或再生HCs上的静纤毛。