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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

Mitochondria are key metabolic organelles that exhibit a high level of phenotypic plasticity in skeletal muscle. The import of proteins from the cytosol is a critical pathway for organelle biogenesis, essential for the expansion of the reticulum and the maintenance of mitochondrial function. Therefore, protein import serves as a barometer of cellular health.

Abstract

Mitochondria are key metabolic and regulatory organelles that determine the energy supply as well as the overall health of the cell. In skeletal muscle, mitochondria exist in a series of complex morphologies, ranging from small oval organelles to a broad, reticulum-like network. Understanding how the mitochondrial reticulum expands and develops in response to diverse stimuli such as alterations in energy demand has long been a topic of research. A key aspect of this growth, or biogenesis, is the import of precursor proteins, originally encoded by the nuclear genome, synthesized in the cytosol, and translocated into various mitochondrial sub-compartments. Mitochondria have developed a sophisticated mechanism for this import process, involving many selective inner and outer membrane channels, known as the protein import machinery (PIM). Import into the mitochondrion is dependent on viable membrane potential and the availability of organelle-derived ATP through oxidative phosphorylation. Therefore its measurement can serve as a measure of organelle health. The PIM also exhibits a high level of adaptive plasticity in skeletal muscle that is tightly coupled to the energy status of the cell. For example, exercise training has been shown to increase import capacity, while muscle disuse reduces it, coincident with changes in markers of mitochondrial content. Although protein import is a critical step in the biogenesis and expansion of mitochondria, the process is not widely studied in skeletal muscle. Thus, this paper outlines how to use isolated and fully functional mitochondria from skeletal muscle to measure protein import capacity in order to promote a greater understanding of the methods involved and an appreciation of the importance of the pathway for organelle turnover in exercise, health, and disease.

Introduction

Mitochondria are organelles that exist in complex morphologies in different cell types and are recognized to possess an increasing array of functions that are critical for cellular health. As such, they can no longer be whittled down merely to energy-producing organelles. Mitochondria are key metabolic regulators, determinants of cell fate, and signaling hubs, the functions of which can serve as useful indicators of overall cellular health. In skeletal muscle cells, electron microscopy studies reveal the presence of geographically distinct subsarcolemmal (SS) and intermyofibrillar (IMF) mitochondria, which exhibit a degree of connectivity1....

Protocol

All animals used in these experiments are maintained in the animal care facility at York University. The experiments are conducted in accordance with the Canadian Council on Animal Care guidelines with approval from the York University Animal Care Committee (Permit: 2017-08).

1. Functional isolation of subsarcolemmal and intermyofibrillar mitochondria from skeletal muscle

  1. Reagent preparation:
    1. Prepare all the buffers and media as mentioned in Table 1.

Representative Results

We have extensively illustrated that this protocol is a valid assay for determining the rate of import into functional and intact isolated skeletal muscle mitochondria. In comparison to untreated conditions, the import of typical precursor proteins such as malate dehydrogenase (MDH) into the matrix is sensitive to membrane potential because it can be inhibited by valinomycin, a respiratory chain uncoupler (Figure 2A). Import is also impeded when mitochondrial inner and outer.......

Discussion

Mitochondria are uniquely dependent on the expression and coordination of both the nuclear and mitochondrial genomes for their synthesis and expansion within cells. However, the nuclear genome encodes the vast majority (99%) of the mitochondrial proteome, and this underscores the importance of the protein import machinery in supporting mitochondrial biogenesis. Import also serves as an important signaling event, as failure to import can promote the initiation of the unfolded protein response and/or mitophagy

Acknowledgements

The authors would like to thank Dr. G.C. Shore of McGill University, Dr. A. Strauss of the Washington School of Medicine, and Dr. M.T. Ryan of La Trobe University for the original donations of expression plasmids that were used for this research. This work was supported by funding from the Natural Sciences and Engineering Research Council of Canada (NSERC) to D. A. Hood. D. A. Hood is also the holder of a Canada Research Chair in Cell Physiology.

....

Materials

NameCompanyCatalog NumberComments
0.2% BSASigmaA2153
35S-methioninePerkin ElmerNEG709A500UCPurchase requires a valid radioisotope permit
ATPSigmaA7699
Blotting paper; Whatman 3MM CHR PaperThermo Fisher05-714-5
Cassette for filmKodakKodak Xomatic
Centrifugation TubeThermo Fisher3138-0050
ChloroformThermo FisherC298-4
DTTSigmaD9779-5G
EDTABioShopEDT002
EGTASigmaE4378
Gel DryerBioRadModel 583
Gel Drying KitSigma or BioRadZ377570-1PAK or OW-GDF-10Various options are commercially available through many companies, these are just as few examples.
GlycerolCaledon Laboratory Chemicals5350-1-40
HEPESSigmaH3375
High Speed CentrifugeBeckman CoulterAvanti J-25 Centrifuge
HomogenizerIKAT25 Digital Ultra Turrex
Isoamylalcohol, or 3-methylbutanolSigmaI9392
KAcBioShopPOA301.500
KClSigmaP3911
M7GNew England BiolabS1404SDilute with 1000ul 20mM HEPES to make 1mM stock
MgClBioShopMAG510
MgSO4Thermo FisherM65-500
MOPSBioShopMOP001
NaClBioShopSOD001
NTPThermo FisherR0191
OCT Plasmid--Donated from Dr. G. C. Shore, McGill University, Montreal, Canada; alternative available through Addgene, plasmid #71877
pGEM4Z/hTom40 Plasmid--Donated from Dr. M. T. Ryan, La Trobe University, Melbourne, Australia
pGMDH Plasmid--Donated from Dr. A. Strauss, Washington University School of Medicine
PhenolSigmaP4557
Phenol:Chloroform:IsoamyalcoholSigmaP3803Can also be made with the ratio provided
Phosphorus FilmFujifilmBAS-IP MS 2025
Rabbit reticulocyte lysatePromegaL4960Avoid freeze-thaw; aliquot lysate upon arrival; amino acids are provided in the kit as well
RNAsinPromegaN2311
Rotor for High Speed CentrifugeBeckman CoulterJA-25.50
SDSBioShopSDS001.500Caution: harmful if ingested or inhaled, wear a mask.
Sodium acetateBioshopSAA 304
Sodium CarbonateVWRBDH9284
Sodium salicylateMillipore Sigma106601
SorbitolSigmaS6021
SP6 RNA PolymerasePromegaP1085
SpectrophotometerThermo FisherNanodrop 2000
SpermidineSigmaS-2626
SucroseBioShopSUC507
T7 RNA PolymerasePromegaP2075
Tabletop CentrifugeThermo FisherAccuSpin Micro 17
Trichloroacetic acidThermo FisherA322-500
TrisBioShopTRS001
β-mercaptoethanolSigmaM6250-100ML

References

  1. Kirkwood, S. P., Munn, E. A., Brooks, G. A. Mitochondrial reticulum in limb skeletal muscle. The American Journal of Physiology. 251 (3), 395-402 (1986).
  2. Glancy, B., et al. Power grid protection of the muscle mitochondrial reticulum.

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MitochondriaProtein ImportSkeletal MuscleBiochemical TechniqueIsolationViabilityIntegrityHomogenizationCentrifugationResuspensionIn Vitro TranslationImport Assay

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