Wide-field montage on transmission electron microscopy via network tele-microscopy enables quantitative analysis of mouse olfactory bulb neural circuits.

IF 1.9
Haruyo Yamanishi, Emi Kiyokage, Satoshi Ichikawa, Kaoru Mitsuoka, Kazunori Toida
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Abstract

Transmission electron microscopy (TEM) provides nanometer-scale resolution, which is essential for ultrastructural analysis of biological tissue. However, its application for large tissue areas is limited by a restricted field of view and observer-dependent sampling. In this study, we present a workflow that combines wide-field montage TEM-via 'network tele-microscopy'-with correlative light and electron microscopy to enable large-area ultrastructural analysis while preserving synapse-level resolution. We demonstrate this approach in the glomerular layer and tyrosine hydroxylase-positive neurons in mouse olfactory bulb glomeruli, which exhibit dense, heterogeneous synaptic organization. Light and confocal laser scanning microscopy were first used for orientation in regions of interest, allowing the generation of continuous wide-field montage TEM datasets. This approach allowed systematic identification and quantification of synapses across an entire glomerulus while maintaining spatial relationships among ultrastructural elements. This study demonstrates a technically feasible platform for the development of TEM and the future integration of network tele-microscopy with computational methods.

通过网络远程显微镜对透射电子显微镜进行宽视场蒙太奇,可以对小鼠嗅球神经回路进行定量分析。
透射电子显微镜(TEM)提供纳米尺度的分辨率,这对生物组织的超微结构分析至关重要。然而,它在大组织区域的应用受到视场限制和观察者依赖采样的限制。在这项研究中,我们提出了一种将宽视场蒙太奇tem(通过“网络远程显微镜”)与相关光学和电子显微镜相结合的工作流程,以实现大面积超微结构分析,同时保持突触级分辨率。我们在小鼠嗅球肾小球的肾小球层和酪氨酸羟化酶阳性神经元中证明了这种方法,这些神经元表现出致密的、异质的突触组织。光和共聚焦激光扫描显微镜首先用于定位感兴趣的区域,允许生成连续的宽视场蒙太奇TEM数据集。这种方法可以系统地识别和量化整个肾小球的突触,同时保持超微结构元素之间的空间关系。该研究为TEM的发展和未来网络远程显微镜与计算方法的整合提供了一个技术上可行的平台。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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