Call to action to properly utilize electron microscopy to measure organelles to monitor disease

IF 4.5 3区 生物学 Q2 CELL BIOLOGY
Kit Neikirk , Edgar-Garza Lopez , Andrea G. Marshall , Ahmad Alghanem , Evan Krystofiak , Bartosz Kula , Nathan Smith , Jianqiang Shao , Prasanna Katti , Antentor Hinton Jr.
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引用次数: 1

Abstract

This review provides an overview of the current methods for quantifying mitochondrial ultrastructure, including cristae morphology, mitochondrial contact sites, and recycling machinery and a guide to utilizing electron microscopy to effectively measure these organelles. Quantitative analysis of mitochondrial ultrastructure is essential for understanding mitochondrial biology and developing therapeutic strategies for mitochondrial-related diseases. Techniques such as transmission electron microscopy (TEM) and serial block face-scanning electron microscopy, as well as how they can be combined with other techniques including confocal microscopy, super-resolution microscopy, and correlative light and electron microscopy are discussed. Beyond their limitations and challenges, we also offer specific magnifications that may be best suited for TEM analysis of mitochondrial, endoplasmic reticulum, and recycling machinery. Finally, perspectives on future quantification methods are offered.

呼吁采取行动,正确利用电子显微镜测量细胞器,以监测疾病。
这篇综述概述了目前量化线粒体超微结构的方法,包括嵴形态、线粒体接触位点和回收机制,并为利用电子显微镜有效测量这些细胞器提供了指南。线粒体超微结构的定量分析对于理解线粒体生物学和制定线粒体相关疾病的治疗策略至关重要。讨论了透射电子显微镜(TEM)和连续块面扫描电子显微镜等技术,以及它们如何与其他技术相结合,包括共焦显微镜、超分辨率显微镜以及相关的光学和电子显微镜。除了它们的局限性和挑战之外,我们还提供了可能最适合线粒体、内质网和回收机制的TEM分析的特定放大倍数。最后,对未来的量化方法进行了展望。
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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来源期刊
European journal of cell biology
European journal of cell biology 生物-细胞生物学
CiteScore
7.30
自引率
1.50%
发文量
80
审稿时长
38 days
期刊介绍: The European Journal of Cell Biology, a journal of experimental cell investigation, publishes reviews, original articles and short communications on the structure, function and macromolecular organization of cells and cell components. Contributions focusing on cellular dynamics, motility and differentiation, particularly if related to cellular biochemistry, molecular biology, immunology, neurobiology, and developmental biology are encouraged. Manuscripts describing significant technical advances are also welcome. In addition, papers dealing with biomedical issues of general interest to cell biologists will be published. Contributions addressing cell biological problems in prokaryotes and plants are also welcome.
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