Yamahara Kohei, Yamamoto Norio, Nakagawa Takayuki, Ito Juichi
Department of Otolaryngology, Head and Neck Surgery, Graduate School of Medicine, Kyoto University, 54 Shogoin Kawahara-cho, Sakyo-ku, Kyoto 606-8507, Japan.
Department of Otolaryngology, Head and Neck Surgery, Graduate School of Medicine, Kyoto University, 54 Shogoin Kawahara-cho, Sakyo-ku, Kyoto 606-8507, Japan.
Hear Res. 2015 Dec;330(Pt A):2-9. doi: 10.1016/j.heares.2015.04.009. Epub 2015 Apr 30.
Sensorineural hearing loss (SNHL) is mainly caused by cochlear hair cell damage. Because cochlear hair cells and supporting cells lose their ability to proliferate in postnatal mammals, SNHL was thought to be an intractable disease. The maintenance of hair cell and supporting cell numbers after cochlear injury is therefore important for the treatment of sensorineural hearing loss. To achieve such treatment, protection and/or regeneration of hair cells is necessary. Progress in cochlear injury research, developmental biology, and regenerative medicine has led to the discovery of cochlear hair cells being protected or regenerated not only by direct reaction of hair cells themselves but also by that of supporting cells. Insulin-like growth factor 1 (IGF1) is considered a novel and potent treatment for SNHL based on the findings of various in vivo and in vitro experiments and clinical trials. The application of IGF1 maintains hair cell number of postnatal mammalian cochleae after various kinds of ototoxicity including aminoglycoside treatment, noise exposure, and ischemia. The positive effects of IGF1 on hair cell damage have been confirmed with in vivo animal experiments; hearing recovery in patients with sudden sensorineural hearing loss refractory to systemic glucocorticoid treatment has also been shown to occur following IGF1 treatment. The mechanisms of IGF1-induced maintenance of hair cell number have been investigated using a cochlear explant culture system, which demonstrated that IGF1 acts on supporting cells, leading to the inhibition of hair cell apoptosis and the proliferation of supporting cells. Netrin1 has furthermore been identified as one of the effectors whose expression is increased by IGF1 treatment.
感音神经性听力损失(SNHL)主要由耳蜗毛细胞损伤引起。由于耳蜗毛细胞和支持细胞在出生后的哺乳动物中失去了增殖能力,SNHL曾被认为是一种难治性疾病。因此,耳蜗损伤后毛细胞和支持细胞数量的维持对于感音神经性听力损失的治疗至关重要。为了实现这种治疗,毛细胞的保护和/或再生是必要的。耳蜗损伤研究、发育生物学和再生医学的进展导致发现耳蜗毛细胞不仅通过自身的直接反应,而且通过支持细胞的反应得到保护或再生。基于各种体内和体外实验以及临床试验的结果,胰岛素样生长因子1(IGF1)被认为是一种治疗SNHL的新型有效方法。IGF1的应用可在包括氨基糖苷类治疗、噪声暴露和缺血在内的各种耳毒性作用后维持出生后哺乳动物耳蜗的毛细胞数量。IGF1对毛细胞损伤的积极作用已在体内动物实验中得到证实;IGF1治疗后,对全身糖皮质激素治疗无效的突发性感音神经性听力损失患者的听力也已显示有所恢复。已使用耳蜗外植体培养系统研究了IGF1诱导毛细胞数量维持的机制,结果表明IGF1作用于支持细胞,导致毛细胞凋亡的抑制和支持细胞的增殖。此外,Netrin1已被确定为其表达因IGF1治疗而增加的效应分子之一。