Selivanova Oxana, Brieger Jürgen, Heinrich Ulf-Rüdiger, Mann Wolf
Department of Otorhinolaryngology, Mainz Medical School, Mainz, Germany.
ORL J Otorhinolaryngol Relat Spec. 2007;69(5):277-82. doi: 10.1159/000103871. Epub 2007 Jun 12.
The molecular mechanisms induced in the inner ear after noise exposure are not well understood. Akt and c-Jun N-terminal kinase (JNK) are key factors of signaling pathways balancing cellular survival and apoptosis. Therefore, we analyzed the spatial distribution of Akt, JNK, their respective activated (i.e. phosphorylated) forms, p-Akt and p-JNK, as well as NF kappa B by immunohistochemistry after 70- and 90-dB noise exposure in an animal model. Alterations of the expression patterns compared to unexposed animals were quantified by a computer-based image analysis method. In unexposed specimens, Akt, p-Akt, JNK, p-JNK were found to be commonly expressed in different regions of the cochlea, whereas NF kappa B was exclusively restricted to the lateral wall. After noise stimulation, the expression of the different molecules was downregulated with the exception of JNK. JNK remained largely unchanged or increased JNK levels were identified in ganglion cells and Schwann cells after 70 dB as well as in the unstained nerve fibers. The stable or increasing levels of JNK might be indicative of a preapoptotic state. The downregulation of Akt in the cochlea might support these activities. p-Akt was not reduced in the spiral ganglion cells after 90-dB exposure and was upregulated in the unstained nerve fibers, probably indicating a counteracting prosurvival cellular reaction in these tissues. In conclusion, we suggest that the observed alterations in both the Akt and JNK pathways are part of a noise distress-induced response indicating pro- and antiapoptotic activities in the different tissues of the cochlea.
噪声暴露后内耳诱导的分子机制尚未完全明确。Akt和c-Jun氨基末端激酶(JNK)是平衡细胞存活和凋亡的信号通路的关键因子。因此,我们通过免疫组织化学分析了动物模型在70分贝和90分贝噪声暴露后Akt、JNK、它们各自的活化(即磷酸化)形式p-Akt和p-JNK以及核因子κB的空间分布。通过基于计算机的图像分析方法对与未暴露动物相比的表达模式变化进行了量化。在未暴露的标本中,发现Akt、p-Akt、JNK、p-JNK在耳蜗的不同区域普遍表达,而核因子κB仅局限于侧壁。噪声刺激后,除JNK外,不同分子的表达均下调。70分贝噪声暴露后,JNK在很大程度上保持不变,或在神经节细胞和施万细胞以及未染色的神经纤维中JNK水平升高。JNK水平稳定或升高可能表明处于凋亡前期状态。耳蜗中Akt的下调可能支持这些活动。90分贝暴露后,螺旋神经节细胞中的p-Akt没有降低,且在未染色的神经纤维中上调,这可能表明这些组织中存在对抗细胞存活的反应。总之,我们认为观察到的Akt和JNK通路的改变是噪声应激诱导反应的一部分,表明耳蜗不同组织中存在促凋亡和抗凋亡活动。