人体耳蜗的免疫监视和保护

Wei Liu, Hao Li, Charlotta Kämpfe Nordström, N. Danckwardt-Lillieström, S. Agrawal, H. Ladak, Helge Rask-Andersen
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引用次数: 0

摘要

尽管人类的内耳位于感染高发区附近,但它却表现出惊人的恢复力。这表明,有一些固有的工具可以阻止病原体侵入和扩散到内耳。在这里,我们将高分辨率光学显微镜、超分辨率免疫组化(SR-SIM)和同步加速器相衬成像(SRC-PCI)结合起来,以侧壁、螺旋神经节和内淋巴囊为重点,识别人内耳各部分的保护和屏障系统。使用 SR-PCI 和尸体标本的三维重建估算声调位置。对切片进行了白细胞和巨噬细胞活性分析,并使用共聚焦显微镜和 SR-SIM 将结果与免疫组化相关联。免疫组化显示,IBA1细胞经常在螺旋神经节、神经纤维、侧壁、螺旋缘、耳蜗所有转折处的鼓膜覆盖层以及内淋巴囊共同表达MHC II。RNAscope 分析显示,I 型螺旋神经节细胞中广泛表达 fractalkine 基因转录本。CD4 和 CD8 细胞偶尔会包围模耳和侧壁的血管。TMEM119和P2Y12没有表达,表明用IBA1标记的细胞不是小胶质细胞。结果表明,人类耳蜗受到居住和循环免疫细胞的监视。研究结果表明,人类耳蜗受到居住和循环免疫细胞的监视。居住和血液传播的巨噬细胞可能通过侧壁、螺旋膜和螺旋神经节不同频率位置的趋化因子信号,启动保护性免疫反应。同步加速器成像揭示了耳蜗底部令人感兴趣的保护屏障。本文讨论了内淋巴囊在人类内耳先天性和适应性免疫中的作用。
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Immuno-surveillance and protection of the human cochlea
Despite its location near infection-prone areas, the human inner ear demonstrates remarkable resilience. This suggests that there are inherent instruments deterring the invasion and spread of pathogens into the inner ear. Here, we combined high-resolution light microscopy, super-resolution immunohistochemistry (SR-SIM) and synchrotron phase contrast imaging (SR-PCI) to identify the protection and barrier systems in the various parts of the human inner ear, focusing on the lateral wall, spiral ganglion, and endolymphatic sac.Light microscopy was conducted on mid-modiolar, semi-thin sections, after direct glutaraldehyde/osmium tetroxide fixation. The tonotopic locations were estimated using SR-PCI and 3D reconstruction in cadaveric specimens. The sections were analyzed for leucocyte and macrophage activity, and the results were correlated with immunohistochemistry using confocal microscopy and SR-SIM.Light microscopy revealed unprecedented preservation of cell anatomy and several macrophage-like cells that were localized in the cochlea. Immunohistochemistry demonstrated IBA1 cells frequently co-expressing MHC II in the spiral ganglion, nerve fibers, lateral wall, spiral limbus, and tympanic covering layer at all cochlear turns as well as in the endolymphatic sac. RNAscope assays revealed extensive expression of fractalkine gene transcripts in type I spiral ganglion cells. CD4 and CD8 cells occasionally surrounded blood vessels in the modiolus and lateral wall. TMEM119 and P2Y12 were not expressed, indicating that the cells labeled with IBA1 were not microglia. The round window niche, compact basilar membrane, and secondary spiral lamina may form protective shields in the cochlear base.The results suggest that the human cochlea is surveilled by dwelling and circulating immune cells. Resident and blood-borne macrophages may initiate protective immune responses via chemokine signaling in the lateral wall, spiral lamina, and spiral ganglion at different frequency locations. Synchrotron imaging revealed intriguing protective barriers in the base of the cochlea. The role of the endolymphatic sac in human inner ear innate and adaptive immunity is discussed.
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