Someya Shinichi, Xu Jinze, Kondo Kenji, Ding Dalian, Salvi Richard J, Yamasoba Tatsuya, Rabinovitch Peter S, Weindruch Richard, Leeuwenburgh Christiaan, Tanokura Masaru, Prolla Tomas A
Department of Genetics and Medical Genetics, Veterans Administration Hospital, Geriatric Research Education and Clinical Center, University of Wisconsin, Madison, WI 53706, USA.
Proc Natl Acad Sci U S A. 2009 Nov 17;106(46):19432-7. doi: 10.1073/pnas.0908786106. Epub 2009 Nov 9.
Age-related hearing loss (AHL), known as presbycusis, is a universal feature of mammalian aging and is the most common sensory disorder in the elderly population. The molecular mechanisms underlying AHL are unknown, and currently there is no treatment for the disorder. Here we report that C57BL/6J mice with a deletion of the mitochondrial pro-apoptotic gene Bak exhibit reduced age-related apoptotic cell death of spiral ganglion neurons and hair cells in the cochlea, and prevention of AHL. Oxidative stress induces Bak expression in primary cochlear cells, and Bak deficiency prevents apoptotic cell death. Furthermore, a mitochondrially targeted catalase transgene suppresses Bak expression in the cochlea, reduces cochlear cell death, and prevents AHL. Oral supplementation with the mitochondrial antioxidants alpha-lipoic acid and coenzyme Q(10) also suppresses Bak expression in the cochlea, reduces cochlear cell death, and prevents AHL. Thus, induction of a Bak-dependent mitochondrial apoptosis program in response to oxidative stress is a key mechanism of AHL in C57BL/6J mice.
年龄相关性听力损失(AHL),即老年性耳聋,是哺乳动物衰老的普遍特征,也是老年人群中最常见的感觉障碍。AHL背后的分子机制尚不清楚,目前该疾病尚无治疗方法。在此我们报告,缺失线粒体促凋亡基因Bak的C57BL/6J小鼠,其耳蜗螺旋神经节神经元和毛细胞的年龄相关性凋亡细胞死亡减少,且预防了AHL。氧化应激诱导原代耳蜗细胞中Bak表达,而Bak缺陷可防止凋亡细胞死亡。此外,线粒体靶向过氧化氢酶转基因可抑制耳蜗中Bak表达,减少耳蜗细胞死亡,并预防AHL。口服线粒体抗氧化剂α-硫辛酸和辅酶Q10也可抑制耳蜗中Bak表达,减少耳蜗细胞死亡,并预防AHL。因此,响应氧化应激诱导的依赖Bak的线粒体凋亡程序是C57BL/6J小鼠AHL的关键机制。