Department of Neuroscience, Tufts University School of Medicine, Boston, Massachusetts 02111, USA.
J Neurosci Res. 2010 Oct;88(13):2976-90. doi: 10.1002/jnr.22449.
Generation of reactive oxygen species (ROS) is a common denominator in many conditions leading to cell death in the cochlea, yet little is known of the cochlea's endogenous mechanisms involved in preventing oxidative stress and its consequences in the cochlea. We have recently described a corticotropin-releasing factor (CRF) signaling system in the inner ear involved in susceptibility to noise-induced hearing loss. We use biochemical and proteomics assays to define further the role of CRF signaling in the response of cochlear cells to aminoglycoside exposure. We demonstrate that activity via the CRF(2) class of receptors protects against aminoglycoside-induced ROS production and activation of cell death pathways. This study suggests for the first time a role for CRF signaling in protecting the cochlea against oxidative stress, and our proteomics data suggest novel mechanisms beyond induction of free radical scavengers that are involved in its protective mechanisms.
活性氧(ROS)的产生是许多导致耳蜗细胞死亡的情况的共同特征,但对于耳蜗中涉及预防氧化应激及其后果的内源性机制知之甚少。我们最近描述了内耳中的促肾上腺皮质释放因子(CRF)信号系统,该系统与噪声性听力损失的易感性有关。我们使用生化和蛋白质组学检测来进一步定义 CRF 信号在耳蜗细胞对氨基糖苷类暴露的反应中的作用。我们证明,通过 CRF(2)类受体的活性可防止氨基糖苷类诱导的 ROS 产生和细胞死亡途径的激活。这项研究首次表明 CRF 信号在保护耳蜗免受氧化应激方面的作用,并且我们的蛋白质组学数据表明,除了诱导自由基清除剂之外,还涉及到其保护机制的新机制。