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鼠中枢神经系统髓鞘形成的透射电镜分析。

Transmission electron microscopic analysis of myelination in the murine central nervous system.

机构信息

Department of Neurology, School of Medicine, University of California, Davis, Sacramento, CA 95817, USA.

Institute for Pediatric Regenerative Medicine (IPRM), Shriners Hospitals for Children - Northern California, Sacramento, CA 95817, USA.

出版信息

STAR Protoc. 2022 Apr 18;3(2):101304. doi: 10.1016/j.xpro.2022.101304. eCollection 2022 Jun 17.

Abstract

Myelin provides physical, neurotrophic, and metabolic support for axonal integrity. The thickness of CNS (central nervous system) myelin sheath is usually < one micrometer, which is under or near the detection threshold of the conventional light microscopy. Here, we present a high-resolution transmission electron microscopy-based protocol to assess myelination at the ultrastructural level. We describe sample preparation from mouse tissue, followed by electron microscopic imaging and CNS myelination analysis. This protocol is also useful for analyzing murine PNS myelination. For complete details on the use and execution of this protocol, please refer to Wang et al. (2021).

摘要

髓鞘为轴突完整性提供物理、神经营养和代谢支持。中枢神经系统 (CNS) 髓鞘的厚度通常 < 1 微米,低于或接近常规光学显微镜的检测阈值。在这里,我们提供了一种基于高分辨率透射电子显微镜的方案,用于在超微结构水平上评估髓鞘形成。我们描述了从小鼠组织中进行样本制备,然后进行电子显微镜成像和 CNS 髓鞘分析。该方案也可用于分析小鼠周围神经系统的髓鞘形成。有关该方案使用和执行的完整详细信息,请参阅 Wang 等人。(2021)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d887/9043565/fa83edf7b898/fx1.jpg

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