Département d'Otoneurologie, CHU Lille, Université de Lille 2 Henri-Warembourg, 59000 Lille, France; Unité INSERM U1008-Controlled Drug Delivery Systems and Biomaterials, 59000 Lille, France.
Département d'Otoneurologie, CHU Lille, Université de Lille 2 Henri-Warembourg, 59000 Lille, France; Unité INSERM U1008-Controlled Drug Delivery Systems and Biomaterials, 59000 Lille, France.
Eur Ann Otorhinolaryngol Head Neck Dis. 2022 Nov;139(6):333-336. doi: 10.1016/j.anorl.2022.03.002. Epub 2022 Jul 5.
To assess a clearing protocol using ethyl cinnamate, an organic substance which is non-toxic for humans, and its value in light-sheet microscopy study of post-implantation cochlear damage in the Mongolian gerbil.
The animals underwent right cochlear implantation in the round window by a retroauricular approach. They were then euthanized 10 weeks after implantation (electrode array in place). The cochleae were prepared according to a 29-day protocol including steps of fixation, microdissection, decalcification, permeabilization, blocking, fluorescent immunolabeling, dehydration and finally clearing in ethyl cinnamate solution. Acquisition of transparent cochleae was performed by light-sheet microscopy. Imaris software was then used for 3D analysis.
The transparent cochleae had not undergone any shrinkage or any significant architectural changes. Six cochleae were acquired by light-sheet microscopy, allowing good visibility of the whole cochlea. 3D immunofluorescence analysis of the cochlea provided sufficient image resolution for analysis of the spiral ganglion neurons and assessment of the fibrotic tissue reaction surrounding the electrode array.
The ethyl cinnamate clearing protocol was effective for light-sheet microscopy analysis of the whole Mongolian gerbil cochlea with the implant left in situ. This technique is suitable for the study of post-implantation cell and tissue damage in the same sample, without the potential toxicity of other methods described to date.
评估一种使用肉桂酸乙酯的透明化方案,肉桂酸乙酯是一种对人类无毒的有机物质,并评估其在光片显微镜下研究蒙古沙鼠植入后耳蜗损伤中的价值。
动物通过耳后入路进行右耳蜗植入。植入后 10 周(电极阵列在位)将其处死。根据包括固定、微解剖、脱钙、通透、阻断、荧光免疫标记、脱水和最后在肉桂酸乙酯溶液中透明化的 29 天方案来制备耳蜗。通过光片显微镜获取透明耳蜗。然后使用 Imaris 软件进行 3D 分析。
透明耳蜗未发生任何收缩或明显的结构变化。通过光片显微镜获得了 6 个耳蜗,可以很好地观察整个耳蜗。耳蜗的 3D 免疫荧光分析提供了足够的图像分辨率,可用于分析螺旋神经节神经元和评估围绕电极阵列的纤维组织反应。
肉桂酸乙酯透明化方案对于原位植入物的整个蒙古沙鼠耳蜗的光片显微镜分析是有效的。该技术适用于同一样本中植入后细胞和组织损伤的研究,而没有迄今为止描述的其他方法的潜在毒性。