Department of Chemical Engineering, National Tsing Hua University, Hsinchu, Taiwan.
Neurogastroenterol Motil. 2011 Oct;23(10):e446-57. doi: 10.1111/j.1365-2982.2011.01773.x. Epub 2011 Sep 4.
Due to the dispersed nature of neurites and fibers, the microtome-based 2-dimensional histology provides only a limited perspective of the enteric nervous system. To visualize the enteric plexus, we applied optical clearing to avoid scattering in the human ileum to facilitate photon penetration for 3-dimensional (3-D) microscopy of the neural tissue.
Human ileal specimens were derived by trimming the donor bowel due to its excess length during the clinical trial of small intestinal transplantation. The pan-neuronal marker PGP9.5 was used as the immunostaining target to reveal the enteric plexuses. The labeled tissues were immersed in the optical-clearing solution prior to deep-tissue confocal microscopy. The serial sections were digitally analyzed and processed by reconstruction algorithms for 3-D visualization.
Optical clearing of the ileal specimen led to less fluorescence signal decay along the focal path in the tissue and a higher signal-to-noise ratio of the confocal micrographs in comparison with the untreated saline control. Taking advantage of the high signal-to-noise ratio images, we applied software-based signal analysis to identify the presence of the nerve fibers and quantify the signal peaks. The image stacks derived from the serial anatomic micrographs created panoramic views of the gut wall innervations with their associated microstructures.
CONCLUSIONS & INFERENCES: We provide an optical approach to improve the imaging depth in 3-D neurohistology of the human ileum. This methodology has significant promise in facilitating our understanding of the enteric nervous system in health and disease.
由于神经突和纤维的分散性质,基于切片机的 2 维组织学仅提供了对肠神经系统的有限视角。为了可视化肠神经丛,我们应用光学透明化来避免人回肠中的散射,以促进光子穿透,从而对神经组织进行 3 维(3-D)显微镜检查。
通过修剪捐赠者肠道的多余长度,从临床小肠移植试验中获得人类回肠标本。使用泛神经元标志物 PGP9.5 作为免疫染色靶标,以揭示肠神经丛。将标记的组织浸入光学透明溶液中,然后进行深层组织共聚焦显微镜检查。通过重建算法对连续切片进行数字分析和处理,以实现 3 维可视化。
与未经处理的盐水对照相比,回肠标本的光学透明化导致组织中沿焦点路径的荧光信号衰减减少,并且共焦显微镜图像的信噪比更高。利用高信噪比图像,我们应用基于软件的信号分析来识别神经纤维的存在并量化信号峰值。从连续解剖学显微照片衍生的图像堆栈创建了带有相关微观结构的肠道壁神经支配的全景视图。
我们提供了一种光学方法来改善人回肠 3-D 神经组织学的成像深度。这种方法在促进我们对健康和疾病中的肠神经系统的理解方面具有重要意义。