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听觉系统中与年龄相关的环鸟苷酸-腺苷酸合酶-干扰素基因信号刺激物的激活与 C57BL/6J 雄性小鼠的 presbycusis 有关。

Age-related Activation of Cyclic GMP-AMP synthase-Stimulator of Interferon Genes Signaling in the Auditory System is Associated with Presbycusis in C57BL/6J Male Mice.

机构信息

Department of Otolaryngology-Head & Neck Surgery, First Afliated Hospital of Guangxi Medical University, Nanning 530021, Guangxi, China.

Department of Otolaryngology-Head & Neck Surgery, First Afliated Hospital of Guangxi Medical University, Nanning 530021, Guangxi, China.

出版信息

Neuroscience. 2022 Jan 15;481:73-84. doi: 10.1016/j.neuroscience.2021.11.031. Epub 2021 Nov 27.

Abstract

Presbycusis, or age-related hearing loss (ARHL), is primarily associated with sensory or transduction nerve cell degeneration in the peripheral and/or central auditory systems. During aging, the auditory system shows mitochondrial dysfunction and increased inflammatory responses. Mitochondrial dysfunction promotes leakage of mitochondrial DNA (mtDNA) into the cytosol, which activates the cyclic GMP-AMP synthase (cGAS)-stimulator of interferon genes (STING) pathway to induce type I interferon and inflammatory responses. However, whether this pathway is involved in the occurrence and development of ARHL is unknown. This study aimed to determine whether there are age-related changes in the levels of cytosolic mtDNA and cGAS-STING pathway activation in the auditory pathway and to explore their relationship with ARHL. The results showed that cGAS-positive immunoreactive cells were observed in the cochlea, inferior colliculus, and auditory cortex. Levels of cytosolic mtDNA, cGAS, STING, phosphorylated interferon regulatory factor 3, and cytokines were significantly increased in the cochlea, inferior colliculus, and auditory cortex of 6-, 9-, and 12-month-old mice compared with 3-month-old mice. These findings suggested that cytosolic mtDNA may play an important role in the pathogenesis of ARHL by activating cGAS-STING-mediated type I interferon and inflammatory responses.

摘要

老年性聋(presbycusis),又称与年龄相关的听力损失(age-related hearing loss,ARHL),主要与外周和/或中枢听觉系统的感觉或转导神经细胞变性有关。在衰老过程中,听觉系统表现出线粒体功能障碍和炎症反应增加。线粒体功能障碍导致线粒体 DNA(mitochondrial DNA,mtDNA)漏出线粒体进入细胞质,激活环鸟苷酸-腺苷酸合酶(cyclic GMP-AMP synthase,cGAS)-干扰素基因刺激物(stimulator of interferon genes,STING)通路,诱导 I 型干扰素和炎症反应。然而,该通路是否参与 ARHL 的发生发展尚不清楚。本研究旨在确定听觉通路上细胞质 mtDNA 水平和 cGAS-STING 通路激活是否存在与年龄相关的变化,并探讨其与 ARHL 的关系。结果显示,在内耳、下丘和听觉皮层中观察到 cGAS 阳性免疫反应细胞。与 3 月龄小鼠相比,6、9 和 12 月龄小鼠的耳蜗、下丘和听觉皮层中细胞质 mtDNA、cGAS、STING、磷酸化干扰素调节因子 3 和细胞因子水平显著升高。这些发现表明,细胞质 mtDNA 通过激活 cGAS-STING 介导的 I 型干扰素和炎症反应,可能在 ARHL 的发病机制中发挥重要作用。

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