Literature DB >> 30168663

Isolation of mitochondrial subpopulations from skeletal muscle: Optimizing recovery and preserving integrity.

Nicola Lai1,2,3, China M Kummitha1,2,3, Mariana G Rosca4, Hisashi Fujioka5, Bernard Tandler6, Charles L Hoppel5,7,8.   

Abstract

AIM: The subsarcolemmal (SSM) and interfibrillar (IFM) mitochondria in skeletal muscle appear to have distinct biochemical properties affecting metabolism in health and disease. The isolation of mitochondrial subpopulations has been a long-time challenge while the presence of a continuous mitochondrial reticulum challenges the view of distinctive SSM and IFM bioenergetics. Here, a comprehensive approach is developed to identify the best conditions to separate mitochondrial fractions.
METHODS: The main modifications to the protocol to isolate SSM and IFM from rat skeletal muscle were: (a) decreased dispase content and homogenization speed; (b) trypsin treatment of SSM fractions; (c) recentrifugation of mitochondrial fractions at low speed to remove subcellular components. To identify the conditions preserving mitochondrial function, integrity, and maximizing their recovery, microscopy (light and electron) were used to monitor effectiveness and efficiency in separating mitochondrial subpopulations while respiratory and enzyme activities were employed to evaluate function, recovery, and integrity.
RESULTS: With the modifications described, the total mitochondrial yield increased with a recovery of 80% of mitochondria contained in the original skeletal muscle sample. The difference between SSM and IFM oxidative capacity (10%) with complex-I substrate was significant only with a saturated ADP concentration. The inner and outer membrane damage for both subpopulations was <1% and 8%, respectively, while the respiratory control ratio was 16.
CONCLUSION: Using a multidisciplinary approach, conditions were identified to maximize SSM and IFM recovery while preserving mitochondrial integrity, biochemistry, and morphology. High quality and recovery of mitochondrial subpopulations allow to study the relationship between these organelles and disease.
© 2018 Scandinavian Physiological Society. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  electron microscopy; electron transport chain; light microscopy; oxidative phosphorylation; polarography; spectroscopy

Mesh:

Substances:

Year:  2018        PMID: 30168663      PMCID: PMC6335164          DOI: 10.1111/apha.13182

Source DB:  PubMed          Journal:  Acta Physiol (Oxf)        ISSN: 1748-1708            Impact factor:   6.311


  4 in total

1.  Rapid Single-Step Affinity Purification of HA-Tagged Plant Mitochondria.

Authors:  Franziska Kuhnert; Anja Stefanski; Nina Overbeck; Leonie Drews; Andreas S Reichert; Kai Stühler; Andreas P M Weber
Journal:  Plant Physiol       Date:  2019-12-09       Impact factor: 8.340

2.  Integrated approach for data acquisition, visualization and processing of analog polarographic systems for bioenergetics studies.

Authors:  Potter L; Krusienski D; Kennedy J; Hoppel Cl; Lai N
Journal:  Anal Biochem       Date:  2019-12-05       Impact factor: 3.365

Review 3.  Mitochondrial isolation: when size matters.

Authors:  Alexander G Bury; Amy E Vincent; Doug M Turnbull; Paolo Actis; Gavin Hudson
Journal:  Wellcome Open Res       Date:  2020-12-02

4.  Blood volume versus deoxygenated NIRS signal: computational analysis of the effects muscle O2 delivery and blood volume on the NIRS signals.

Authors:  B Koirala; A Concas; Yi Sun; L B Gladden; N Lai
Journal:  J Appl Physiol (1985)       Date:  2021-09-16
  4 in total

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