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Vestibular hair cell regeneration and restoration of balance function induced by math1 gene transfer.

机译:math1基因转移诱导前庭毛细胞再生和平衡功能的恢复。

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摘要

HYPOTHESIS: Delivery of math1 using an adenovector (Admath1.11D) results in vestibular hair cell regeneration and recovery of balance function in ototoxin-treated adult mice. BACKGROUND: Loss of peripheral vestibular function is associated with disease processes such as vestibular neuronitis, aminoglycoside ototoxicity, and aging. Loss of vestibular hair cells is one of the mechanisms underlying balance dysfunction in all of these disorders. Currently, recovery from these diseases relies on central vestibular compensation rather than on local tissue recovery. Overexpression of the mammalian atonal homologue math1 has been demonstrated to induce generation of hair cells in neonatal organ of Corti cultures and in the guinea pig cochlea in vivo and could thus provide an approach to local tissue recovery. METHODS: Admath1.11D was applied to cultures of aminoglycoside-treated macular organs or in vivo in a mouse aminoglycoside ototoxicity model. Outcome measures included histologic examination, immunohistochemistry, swim testing, and evaluation of the horizontal vestibulo-ocular reflex. RESULTS: Delivery of math1 resulted in the generation of vestibular hair cells in vitro after aminoglycoside-mediated loss of hair cells. Math1-treated mice showed recovery of the vestibular neuroepithelium within 8 weeks after Admath1.11D treatment. Assessment of animals after vector infusion demonstrated a recovery of vestibular function compared with aminoglycoside-only-treated mice. CONCLUSION: Molecular replacement of math1 may provide a therapeutic means of restoring vestibular function related to vestibular hair cell loss.
机译:假设:使用腺载体(Admath1.11D)传递math1会导致前耳毛细胞再生,并在经毒素处理的成年小鼠中恢复平衡功能。背景:外周前庭功能的丧失与疾病过程有关,例如前庭神经炎,氨基糖苷耳毒性和衰老。在所有这些疾病中,前庭毛细胞的丧失是平衡功能障碍的潜在机制之一。当前,从这些疾病的恢复取决于中央前庭补偿而不是局部组织恢复。哺乳动物的无性同系物math1的过表达已被证明可以在体内Corti培养的新生器官和豚鼠耳蜗中诱导毛细胞的生成,因此可以为局部组织恢复提供一种途径。方法:将Admath1.11D应用于经氨基糖苷处理的黄斑器官的培养或在小鼠氨基糖苷耳毒性模型中的体内培养。结果措施包括组织学检查,免疫组织化学,游泳测试和水平前庭眼反射的评估。结果:在氨基糖苷介导的毛细胞损失之后,math1的交付导致了体外前庭毛细胞的产生。 Math1处理的小鼠在Admath1.11D治疗后8周内显示前庭神经上皮的恢复。与仅使用氨基糖苷治疗的小鼠相比,载体输注后的动物评估显示前庭功能得以恢复。结论:math1分子替代可能提供恢复与前庭毛细胞丢失有关的前庭功能的治疗手段。

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