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心脏组织中线粒体的系统定量超微结构分析方案

Protocol for the Systematic Quantitative Ultrastructural Analysis of Mitochondria in Cardiac Tissue.

作者信息

Schönmehl Rebecca, Winter Lina, Mendelsohn Daniel H, Cheung Wing-Hoi, Wong Ronald Man Yeung, Pabel Steffen, Sossalla Samuel, Brochhausen Christoph

机构信息

Institute of Pathology, Medical Faculty Mannheim, Heidelberg University, 68167 Mannheim, Germany.

Department of Neurology, LMU University Hospital, LMU Munich, 81377 Munich, Germany.

出版信息

Methods Protoc. 2025 Aug 2;8(4):87. doi: 10.3390/mps8040087.

DOI:10.3390/mps8040087
PMID:40863737
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12388055/
Abstract

Mitochondria play a crucial role in adapting to fluctuating energy demands, particularly in various heart diseases. In addition to functional analyses such as the measurement of ROS or ATP, analysis of mitochondrial ultrastructure can be used to draw further conclusions about their functions and effects in tissue. In this protocol, we introduce a set of measurements to compare the ultrastructural and functional characteristics of human left ventricular mitochondria, using transmission electron microscopy (TEM). Measured parameters included mean size in µm, elongation, count, percental mitochondrial area in the measuring frame, and a conglomeration score. We also introduce a novel method of defining hydropic mitochondria as a comparable evaluation standard. With this cluster of measurement parameters, we aim to contribute a protocol for studying human mitochondrial morphology, distribution, and functionality.

摘要

线粒体在适应能量需求波动方面发挥着关键作用,尤其是在各种心脏疾病中。除了进行诸如活性氧(ROS)或三磷酸腺苷(ATP)测量等功能分析外,线粒体超微结构分析可用于进一步推断其在组织中的功能和作用。在本方案中,我们介绍了一组测量方法,使用透射电子显微镜(TEM)来比较人类左心室线粒体的超微结构和功能特征。测量参数包括以微米为单位的平均大小、伸长率、数量、测量框架中线粒体面积的百分比以及聚集分数。我们还引入了一种将水肿性线粒体定义为可比评估标准的新方法。通过这组测量参数,我们旨在提供一个研究人类线粒体形态、分布和功能的方案。

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本文引用的文献

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Mitochondrial Dysfunction in Cardiac Disease: The Fort Fell.心脏病中的线粒体功能障碍:堡垒陷落。
Biomolecules. 2024 Nov 29;14(12):1534. doi: 10.3390/biom14121534.
2
Mitochondrial Alterations in Alzheimer's Disease: Insight from the 5xFAD Mouse Model.阿尔茨海默病中的线粒体改变:来自5xFAD小鼠模型的见解
Mol Neurobiol. 2025 Jun;62(6):7075-7092. doi: 10.1007/s12035-024-04632-4. Epub 2024 Dec 11.
3
Comparative Analysis of Mitochondria Surrounding the Intercalated Discs in Heart Diseases-An Ultrastructural Pilot Study.比较分析心脏病中心肌闰盘周围的线粒体-一项超微结构初步研究。
Int J Mol Sci. 2024 Jul 12;25(14):7644. doi: 10.3390/ijms25147644.
4
Mitochondrial Structure and Function in Human Heart Failure.线粒体结构和功能在人类心力衰竭中的作用。
Circ Res. 2024 Jul 5;135(2):372-396. doi: 10.1161/CIRCRESAHA.124.323800. Epub 2024 Jul 4.
5
Mitochondrial dysfunction: mechanisms and advances in therapy.线粒体功能障碍:机制与治疗进展。
Signal Transduct Target Ther. 2024 May 15;9(1):124. doi: 10.1038/s41392-024-01839-8.
6
Mitochondria in disease: changes in shapes and dynamics.线粒体在疾病中的作用:形态和动力学的变化。
Trends Biochem Sci. 2024 Apr;49(4):346-360. doi: 10.1016/j.tibs.2024.01.011. Epub 2024 Feb 23.
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Disrupted brain mitochondrial morphology after in vivo hydrogen sulfide exposure.体内硫化氢暴露后大脑线粒体形态的破坏。
Sci Rep. 2023 Oct 24;13(1):18129. doi: 10.1038/s41598-023-44807-y.
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Mitochondrial dynamics in health and disease: mechanisms and potential targets.线粒体动态平衡在健康和疾病中的作用:机制与潜在靶点
Signal Transduct Target Ther. 2023 Sep 6;8(1):333. doi: 10.1038/s41392-023-01547-9.
9
Three-dimensional mitochondria reconstructions of murine cardiac muscle changes in size across aging.三维重构的衰老小鼠心肌线粒体大小变化。
Am J Physiol Heart Circ Physiol. 2023 Nov 1;325(5):H965-H982. doi: 10.1152/ajpheart.00202.2023. Epub 2023 Aug 25.
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Mitochondrial cristae in health and disease.健康与疾病状态下的线粒体嵴
Int J Biol Macromol. 2023 Apr 30;235:123755. doi: 10.1016/j.ijbiomac.2023.123755. Epub 2023 Feb 20.