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噪声性损伤耳蜗中促炎细胞因子的表达

Proinflammatory cytokines expression in noise-induced damaged cochlea.

作者信息

Fujioka Masato, Kanzaki Sho, Okano Hirotaka James, Masuda Masatsugu, Ogawa Kaoru, Okano Hideyuki

机构信息

Department of Otolaryngology, Head and Neck Surgery, Keio University School of Medicine, Tokyo, Japan.

出版信息

J Neurosci Res. 2006 Mar;83(4):575-83. doi: 10.1002/jnr.20764.

DOI:10.1002/jnr.20764
PMID:16429448
Abstract

Recent studies have showed that inflammatory responses occur in inner ear under various damaging conditions including noise-overstimulation. We evaluated the time-dependent expression of proinflammatory cytokines in noise-exposed rat cochlea. Among several detected cytokines, real-time RT-PCR showed that interleukin-1beta (IL-1beta) and interleukin-6 (IL-6) were significantly induced 3 hr after noise exposure, and quickly downregulated to the basal level. Tumor necrosis factor-alpha (TNF-alpha) was also slightly upregulated immediately after noise exposure. Immunohistochemical analysis showed that IL-6 expression was distinctively induced within the lateral side of the spiral ligament. Sequential expression analysis showed that IL-6 immunoreactivity was initially found in the cytoplasm of lateral wall cells, including Type IV and III fibrocytes, and expanded broader throughout the lateral wall, finally to the stria vascularis. Because of the negative Iba-1 staining, IL-6 expression in the early-phase was not due to macrophage or microglia activation. IL-6 was also detected in spiral ganglion neurons at 12 and 24 hr after noise exposure. Our data demonstrates the production of proinflammatory cytokines, including TNF-alpha, IL-1beta, and IL-6, in early phase of noise overstimulated cochlea. IL-6 expression was observed in the spiral ligament, stria vascularis, and spiral ganglion neurons. These cytokines, produced by the cochlear structure itself in response to noise exposure, may initiate an inflammatory response and have some role in the mechanism of noise-induced cochlear damage.

摘要

最近的研究表明,在包括噪声过度刺激在内的各种损伤条件下,内耳会发生炎症反应。我们评估了噪声暴露大鼠耳蜗中促炎细胞因子的时间依赖性表达。在检测到的几种细胞因子中,实时逆转录聚合酶链反应显示,噪声暴露3小时后,白细胞介素-1β(IL-1β)和白细胞介素-6(IL-6)显著诱导,并迅速下调至基础水平。肿瘤坏死因子-α(TNF-α)在噪声暴露后也立即略有上调。免疫组织化学分析显示,IL-6表达在螺旋韧带外侧显著诱导。序列表达分析显示,IL-6免疫反应最初在包括IV型和III型纤维细胞在内的侧壁细胞胞质中发现,并在整个侧壁更广泛地扩展,最终到达血管纹。由于Iba-1染色阴性,早期IL-6表达不是由于巨噬细胞或小胶质细胞激活。噪声暴露后12小时和24小时,螺旋神经节神经元中也检测到IL-6。我们的数据表明,在噪声过度刺激的耳蜗早期会产生包括TNF-α、IL-1β和IL-6在内的促炎细胞因子。在螺旋韧带、血管纹和螺旋神经节神经元中观察到IL-6表达。这些由耳蜗结构自身对噪声暴露产生的细胞因子可能引发炎症反应,并在噪声性耳蜗损伤机制中发挥一定作用。

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