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Role of Spiral Ligament Fibrocytes in Immune-Mediated Inner Ear Damage

螺旋韧带纤维细胞在免疫介导的内耳损伤中的作用

基本信息

批准号：
8306773
负责人：
David J. Lim
金额：
$ 22.13万
依托单位：
HOUSE RESEARCH INSTITUTE
依托单位国家：
美国
项目类别：
财政年份：
2011
资助国家：
美国
起止时间：
2011-08-01 至 2013-07-31
项目状态：
已结题

项目摘要

DESCRIPTION (provided by applicant): Immune-mediated sensorineural hearing loss (IMSNHL) is of clinical importance because of progressive bilateral involvement and potential reversibility. Currently, the therapeutic targets specific to IMSNHL are not available because its molecular pathogenesis is poorly understood. Our long-term goal is to elucidate the molecular mechanism of immune-mediated inner ear damage, resulting in SNHL. Etiopathogenesis of IMSNHL is largely unknown, but regardless of the initiating factors, the final course of IMSNHL is commonly associated with immune-mediated damage of the cochlear cells (sensory and non- sensory). Immune-mediated tissue damage generally involves direct cell-cell signaling via surface molecules such as antibody-dependent cytotoxicity; and indirect signaling via cytokines such as tumor necrosis factor-( (TNF-(). Previously, we have demonstrated that spiral ligament fibrocytes (SLFs) release mediators in response to inflammatory signals and SLF-derived molecules directly attract the inflammatory cells. Therefore, we hypothesize that SLFs are key players in immune-mediated inner ear damage by responding to inflammatory mediators and releasing chemoattractive and cytotoxic molecules. We also found that secretion of TNF-( is required for cisplatin-induced ototoxicity and that down-regulation of TNF-( attenuates cisplatin-induced auditory damage. These results led us to focus on TNF-(-mediated cytotoxicity as a mechanism of immune- mediated inner ear damage. However, the auditory sensory cells appeared to be damaged only by the extremely high concentration of TNF-( in animal experiments, indicating the requirement of sensitization for TNF-(-mediated inner ear cytotoxicity. Therefore, we aim to determine the molecular mechanism involved in: (1) SLF's TNF-( induction in response to IL-1, a model inflammatory mediator; and (2) sensitization of the auditory sensory cells to induce TNF-(-mediated cytotoxicity via interferon-( (IFN-(). In addition, we plan to determine the therapeutic potential of targeting the key molecules involved in IFN-(-sensitized TNF-(-mediated cytotoxicity, which will provide us with a scientific basis for the development of a novel strategy to manage IMSNHL.

描述（由申请方提供）：免疫介导的感音神经性听力损失（IMSNHL）具有临床重要性，因为其进行性双侧受累和潜在可逆性。目前，由于对IMSNHL的分子发病机制知之甚少，还没有针对IMSNHL的特异性治疗靶点。我们的长期目标是阐明免疫介导的内耳损伤的分子机制，导致SNHL。IMSNHL的发病机制在很大程度上是未知的，但无论起始因素如何，IMSNHL的最终过程通常与耳蜗细胞（感觉和非感觉）的免疫介导的损伤相关。免疫介导的组织损伤通常涉及通过表面分子如抗体依赖性细胞毒性的直接细胞-细胞信号传导;和通过细胞因子如肿瘤坏死因子-（TNF-α）的间接信号传导。以前，我们已经证明，螺旋韧带纤维细胞（SLF）释放介质响应炎症信号和SLF衍生的分子直接吸引炎症细胞。因此，我们假设SLF是免疫介导的内耳损伤的关键参与者，通过响应炎症介质和释放化学吸引和细胞毒性分子。我们还发现，分泌TNF-α是顺铂诱导的耳毒性所必需的，下调TNF-α可减轻顺铂诱导的听觉损伤。这些结果使我们关注TNF-α介导的细胞毒性作为免疫介导的内耳损伤的机制。然而，动物实验中，听感觉细胞似乎仅被极高浓度的TNF-α损伤，表明TNF-α介导的内耳细胞毒性需要致敏。因此，我们的目标是确定参与以下过程的分子机制：（1）SLF对IL-1（一种模型炎症介质）的TNF-α诱导;（2）听觉感觉细胞通过干扰素-α（IFN-α）致敏以诱导TNF-α介导的细胞毒性。此外，我们计划确定靶向参与IFN-α致敏TNF-α介导的细胞毒性的关键分子的治疗潜力，这将为我们开发管理IMSNHL的新策略提供科学依据。