» Articles » PMID: 34285964

Transmission Electron Microscopy for Analysis of Mitochondria in Mouse Skeletal Muscle

Overview
Journal Bio Protoc
Specialty Biology
Date 2021 Jul 21
PMID 34285964
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Skeletal muscle is the most abundant tissue in the human body and regulates a variety of functions including locomotion and whole-body metabolism. Skeletal muscle has a plethora of mitochondria, the organelles that are essential for aerobic generation of ATP which provides the chemical energy to fuel vital functions such as contraction. The number of mitochondria in skeletal muscle and their function decline with normal aging and in various neuromuscular diseases and in catabolic conditions such as cancer, starvation, denervation, and immobilization. Moreover, compromised mitochondrial function is also associated with metabolic disorders including type 2 diabetes mellitus. It is now clear that maintaining mitochondrial content and function in skeletal muscle is vital for sustained health throughout the lifespan. While a number of staining methods are available to study mitochondria, transmission electron microscopy (TEM) is still the most important method to study mitochondrial structure and health in skeletal muscle. It provides critical information about mitochondrial content, cristae density, organization, formation of autophagosomes, and any other abnormalities commonly observed in various disease conditions. In this article, we describe a detailed protocol for sample preparation and analysis of mouse skeletal muscle mitochondria by TEM.

Citing Articles

Altered Mitochondrial Morphology and Reduced Cardiolipin Levels in Oocytes of Endometriosis Model Mice: Implications for Mitochondrial Dysfunction in Infertility.

Wijaya O, Anas J, Widjiati W, Widyanugraha M, Samsulhadi S, Bayuaji H Med Sci Monit. 2025; 31:e947194.

PMID: 40040270 PMC: 11892530. DOI: 10.12659/MSM.947194.


The Matrix of Mitochondrial Imaging: Exploring Spatial Dimensions.

Hemel I, Arts I, Moerel M, Gerards M Biomolecules. 2025; 15(2).

PMID: 40001532 PMC: 11853629. DOI: 10.3390/biom15020229.


Mitochondrial Structure and Function in Human Heart Failure.

Hinton Jr A, Claypool S, Neikirk K, Senoo N, Wanjalla C, Kirabo A Circ Res. 2024; 135(2):372-396.

PMID: 38963864 PMC: 11225798. DOI: 10.1161/CIRCRESAHA.124.323800.


A Laing distal myopathy-associated proline substitution in the β-myosin rod perturbs myosin cross-bridging activity.

Buvoli M, Wilson G, Buvoli A, Gugel J, Hau A, Bonnemann C J Clin Invest. 2024; 134(9).

PMID: 38690726 PMC: 11060730. DOI: 10.1172/JCI172599.


Lipopolysaccharide binding protein resists hepatic oxidative stress by regulating lipid droplet homeostasis.

Zhang Q, Shen X, Yuan X, Huang J, Zhu Y, Zhu T Nat Commun. 2024; 15(1):3213.

PMID: 38615060 PMC: 11016120. DOI: 10.1038/s41467-024-47553-5.


References
1.
Peterson C, Johannsen D, Ravussin E . Skeletal muscle mitochondria and aging: a review. J Aging Res. 2012; 2012:194821. PMC: 3408651. DOI: 10.1155/2012/194821. View

2.
Picard M, White K, Turnbull D . Mitochondrial morphology, topology, and membrane interactions in skeletal muscle: a quantitative three-dimensional electron microscopy study. J Appl Physiol (1985). 2012; 114(2):161-71. PMC: 3544498. DOI: 10.1152/japplphysiol.01096.2012. View

3.
Soplop N, Patel R, Kramer S . Preparation of embryos for electron microscopy of the Drosophila embryonic heart tube. J Vis Exp. 2009; (34). PMC: 3143026. DOI: 10.3791/1630. View

4.
Bonnard C, Durand A, Peyrol S, Chanseaume E, Chauvin M, Morio B . Mitochondrial dysfunction results from oxidative stress in the skeletal muscle of diet-induced insulin-resistant mice. J Clin Invest. 2008; 118(2):789-800. PMC: 2176186. DOI: 10.1172/JCI32601. View

5.
Hindi S, Mishra V, Bhatnagar S, Tajrishi M, Ogura Y, Yan Z . Regulatory circuitry of TWEAK-Fn14 system and PGC-1α in skeletal muscle atrophy program. FASEB J. 2013; 28(3):1398-411. PMC: 3929677. DOI: 10.1096/fj.13-242123. View