State Key Laboratory of Digital Medical Engineering, Department of Otolaryngology-Head and Neck Surgery, Zhongda Hospital, School of Life Sciences and Technology, School of Medicine, Advanced Institute for Life and Health, Jiangsu Province High-Tech Key Laboratory for Bio-Medical Research, Southeast University, Nanjing, 210096, China.
Department of Otolaryngology-Head and Neck Surgery, Shandong Provincial ENT Hospital, Shandong University, Jinan, 250022, China.
Adv Sci (Weinh). 2024 Aug;11(29):e2304551. doi: 10.1002/advs.202304551. Epub 2024 May 29.
Mammalian cochlear hair cells (HCs) are essential for hearing, and damage to HCs results in severe hearing impairment. Damaged HCs can be regenerated by neighboring supporting cells (SCs), thus the functional regeneration of HCs is the main goal for the restoration of auditory function in vivo. Here, cochlear SC trans-differentiation into outer and inner HC by the induced expression of the key transcription factors Atoh1 and its co-regulators Gfi1, Pou4f3, and Six1 (GPAS), which are necessary for SCs that are destined for HC development and maturation via the AAV-ie targeting the inner ear stem cells are successfully achieved. Single-cell nuclear sequencing and lineaging tracing results showed that the majority of new Atoh1-derived HCs are in a state of initiating differentiation, while GP (Gfi1, Pou4f3) and GPS (Gfi1, Pou4f3, and Six1) enhanced the Atoh1-induced new HCs into inner and outer HCs. Moreover, the patch-clamp analysis indicated that newborn inner HCs induced by GPAS forced expression have similar electrophysiological characteristics to those of native inner HCs. Also, GPAS can induce HC regeneration in the HC-damaged mice model. In summary, the study demonstrates that AAV-mediated co-regulation of multiple genes, such as GPAS, is an effective means to achieve functional HC regeneration in the mouse cochlea.
哺乳动物耳蜗毛细胞(HCs)是听觉的关键,其损伤会导致严重的听力障碍。相邻的支持细胞(SCs)可以再生受损的 HCs,因此 HCs 的功能再生是体内听觉功能恢复的主要目标。在这里,通过诱导表达关键转录因子 Atoh1 及其共调节因子 Gfi1、Pou4f3 和 Six1(GPAS),可以使耳蜗 SC 转分化为外毛细胞和内毛细胞,这些因子对于通过靶向内耳干细胞的 AAV-ie 内 SC 发育和成熟所必需的。单细胞核测序和谱系追踪结果表明,大多数新的 Atoh1 衍生 HCs 处于起始分化状态,而 GP(Gfi1、Pou4f3)和 GPS(Gfi1、Pou4f3 和 Six1)增强了 Atoh1 诱导的新 HCs 成为内毛细胞和外毛细胞。此外,膜片钳分析表明,由 GPAS 强制表达诱导的新生内毛细胞具有与内源性内毛细胞相似的电生理特征。此外,GPAS 可在 HCs 损伤的小鼠模型中诱导 HCs 再生。总之,该研究表明,AAV 介导的多个基因的共调控,如 GPAS,是在小鼠耳蜗中实现功能性 HCs 再生的有效手段。