Role of the Innate Immune System in the Survival of Auditory Neurons

螺旋神经节神经元将听觉信息从耳蜗毛细胞传递到耳蜗神经元 原子核。因此，螺旋神经节和耳蜗核神经元对正常听力和 聋人通过人工耳蜗术或耳蜗核植入术恢复听力。然而，在某些情况下 在某些情况下，这些神经元可能会在耳聋后退化或死亡，从而限制了这些神经元的潜在疗效 设备。这种神经变性的原因及其在毛细胞死亡后的可变性质尚不清楚。 我们实验室的最新发现表明，先天免疫系统的元素被招募到 耳聋后的螺旋神经节和耳蜗核，提示免疫细胞的激活状态是 这是两个结构中神经元存活的重要决定因素。我们还表明， 先天免疫系统对听觉神经元的存活有深远的影响，在某些情况下 细胞毒性，在其他情况下可能具有神经保护作用。在至少一个耳聋模型中，免疫反应， 值得注意的是，这可能是耳聋后螺旋神经节神经元死亡的主要原因。要解决这些问题 先天免疫系统对听神经元存活的复杂和不同的影响-长期 开发神经保护免疫疗法的目标--我们建议系统地删除特定的 天然免疫系统的组成部分，涉及自然杀伤(NK)细胞、巨噬细胞或小胶质细胞 确定它们对神经元存活的影响。这些实验将使用转基因小鼠，在某些情况下， 抑制性抗体。巨噬细胞和NK细胞都被招募到螺旋神经节对毛发的反应 细胞损伤。拟议中的实验将确定巨噬细胞和NK细胞是否具有神经毒性或 耳蜗神经损伤后的神经保护作用及特异性细胞因子和趋化因子在刺激和恢复过程中的作用 这些免疫细胞的潜在神经毒性。一系列平行的研究将集中在神经免疫方面。 耳蜗核的相互作用，其中一位合作者的广泛研究表明，神经元 存活依赖于在出生后早期成熟的“关键时期”的传入输入。相比之下，成熟的 耳蜗核神经元在去传入的情况下存活。初步数据显示，这可能是由于 小胶质细胞(中枢神经系统的常驻免疫细胞)的神经保护作用拟议中的实验将验证这一点。 假设。总之，这些研究将从根本上测试新的假说，这些假说涉及到 先天免疫系统是神经保护治疗的关键目标，如果不是最佳的话，以提高患者的存活率 耳蜗病理学后的耳蜗神经细胞和听性脑干神经元。

Spiral ganglion neurons transmit auditory information from cochlear hair cells to the neurons of the cochlear nucleus. Thus, spiral ganglion and cochlear nucleus neurons are essential for normal hearing and for restoration of hearing via cochlear or cochlear nucleus implants in deaf individuals. However, in some circumstances these neurons may degenerate or die after deafening, limiting the potential efficacy of these devices. The reasons for this neurodegeneration and its variable nature after hair cell death remain unclear. Recent findings from our labs have revealed that elements of the innate immune system are recruited to the spiral ganglion and cochlear nucleus after deafening and suggest that the activation status of immune cells is an important determinant of neuronal survival in both structures. We also show that these elements of the innate immune system have profound effects on the survival of the auditory neurons, in some cases being cytotoxic, in others possibly neuroprotective. In at least one deafness model, the immune response, remarkably, may be a principal cause of spiral ganglion neuronal death after deafening. To resolve these complex and disparate effects of the innate immune system on auditory neuronal survival – with the long-term goal of developing immunotherapies for neuroprotection – we propose to systematically delete specific components of the innate immune system involving Natural Killer (NK) cells, macrophages, or microglia to determine their effect on neuronal survival. The experiments will use transgenic mice and, in some cases, inhibitory antibodies. Both macrophages and NK cells are recruited into the spiral ganglion in response to hair cell injury. The proposed experiments will determine whether macrophages and NK cells are neurotoxic or neuroprotective in the injured cochlea and the roles of specific cytokines and chemokines in stimulation and potential neurotoxicity of these immune cells. A parallel series of studies will focus on neuroimmune interactions in the cochlear nucleus, in which extensive research by one of the co-PI's has shown that neuronal survival depends on afferent input during a `critical period' in early postnatal maturation. In contrast, mature cochlear nucleus neurons survive deafferentation. Preliminary data suggest that this may be due to neuroprotection by microglia (the resident immune cells of the CNS.) The proposed experiments will test this hypothesis. Together, these studies will test fundamentally new hypotheses implicating specific components of the innate immune system as critical, if not optimal, targets for neuroprotective therapies to promote survival of cochlea and auditory brainstem neurons after cochlear pathology.