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基因和细胞疗法治疗内耳毛细胞的潜力。

Potential of Gene and Cell Therapy for Inner Ear Hair Cells.

机构信息

Department of Otorhinolaryngology and Head & Neck Surgery, Dankook University Hospital, Cheonan, Chungnam, Republic of Korea.

Department of Otolaryngology-Head and Neck Surgery, College of Medicine, Chungnam National University, Daejeon, Republic of Korea.

出版信息

Biomed Res Int. 2018 Jun 13;2018:8137614. doi: 10.1155/2018/8137614. eCollection 2018.

Abstract

Sensorineural hearing loss is caused by the loss of sensory hair cells (HCs) or a damaged afferent nerve pathway to the auditory cortex. The most common option for the treatment of sensorineural hearing loss is hearing rehabilitation using hearing devices. Various kinds of hearing devices are available but, despite recent advancements, their perceived sound quality does not mimic that of the "naïve" cochlea. Damage to crucial cochlear structures is mostly irreversible and results in permanent hearing loss. Cochlear HC regeneration has long been an important goal in the field of hearing research. However, it remains challenging because, thus far, no medical treatment has successfully regenerated cochlear HCs. Recent advances in genetic modulation and developmental techniques have led to novel approaches to generating HCs or protecting against HC loss, to preserve hearing. In this review, we present and review the current status of two different approaches to restoring or protecting hearing, gene therapy, including the newly introduced CRISPR/Cas9 genome editing, and stem cell therapy, and suggest the future direction.

摘要

感音神经性听力损失是由感觉毛细胞(HCs)的丧失或传入听觉皮层的神经通路受损引起的。感音神经性听力损失的最常见治疗选择是使用听力设备进行听力康复。有各种类型的听力设备,但尽管最近取得了进展,它们感知到的声音质量仍无法模仿“原始”耳蜗。耳蜗关键结构的损伤大多是不可逆的,导致永久性听力损失。耳蜗 HC 再生长期以来一直是听力研究领域的重要目标。然而,由于迄今为止,没有任何医疗方法成功地再生了耳蜗 HCs,因此仍然具有挑战性。遗传调控和发育技术的最新进展为产生 HCs 或防止 HC 损失以保护听力提供了新的方法。在这篇综述中,我们介绍并回顾了两种不同的恢复或保护听力的方法的现状,即基因治疗,包括新引入的 CRISPR/Cas9 基因组编辑,以及干细胞治疗,并提出了未来的方向。

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