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Method Article

Measurement of Oxygen Consumption Rates in Intact Caenorhabditis elegans

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DOI:

10.3791/59277

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February 23rd, 2019

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In This Article

Summary

Mitochondrial respiration is critical for organismal survival; therefore, oxygen consumption rate is an excellent indicator of mitochondrial health. In this protocol, we describe the use of a commercially available respirometer to measure basal and maximal oxygen consumption rates in live, intact, and freely-motile Caenorhabditis elegans.

Abstract

Optimal mitochondrial function is critical for healthy cellular activity, particularly in cells that have high energy demands like those in the nervous system and muscle. Consistent with this, mitochondrial dysfunction has been associated with a myriad of neurodegenerative diseases and aging in general. Caenorhabditis elegans have been a powerful model system for elucidating the many intricacies of mitochondrial function. Mitochondrial respiration is a strong indicator of mitochondrial function and recently developed respirometers offer a state-of-the-art platform to measure respiration in cells. In this protocol, we provide a technique to analyze live, intact C. elegans. This protocol spans a period of ~7 days and includes steps for (1) growing and synchronization of C. elegans, (2) preparation of compounds to be injected and hydration of probes, (3) drug loading and cartridge equilibration, (4) preparation of worm assay plate and assay run, and (5) post-experiment data analysis.

Introduction

Adenosine triphosphate (ATP), the main source of cellular energy, is produced in the mitochondria by enzymes in the electron transport chain (ETC) located in the inner mitochondrial membrane. Pyruvate, a key metabolite utilized for mitochondrial ATP production, is imported into the mitochondrial matrix where it is decarboxylated to produce acetyl coenzyme A (CoA). Subsequently, acetyl CoA enters the citric acid cycle resulting in the generation of nicotinamide adenine dinucleotide (NADH), a key electron carrier molecule. As electrons from NADH are passed to oxygen via the ETC, protons build up in the mitochondrial intermembrane space, which results in the generation o....

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Protocol

NOTE: Figure 2 provides a schematic overview of the full protocol.

1. Growth and synchronization of nematode population9,10

  1. Transfer L4 larvae of desired genetic backgrounds (e.g., N2 [wild type] and sel-12 animals) onto nematode growth media (NGM) plates (see Table 1 for recipe) freshly seeded with a lawn of Escherichia coli (OP50)11. Use at least two 100 mm or three 60 mm plates for each strain. Incubate the worms at the appropriate growth temperature (between 15–25 °C) for 3R....

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Results

Using the protocol described herein, OCR of wild type animals and three different sel-12 mutant strains were determined. sel-12 encodes the C. elegans ortholog of presenilin17. Mutations in human presenilin are the most common genetic aberration associated with the development of familial Alzheimer's disease18. Our studies have shown elevated mitochondrial calcium levels in sel-12 mutant animals compared t.......

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Discussion

Mitochondrial respiration is an insightful indicator of mitochondrial function; therefore, being able to measure the oxygen consumption rates in a biological system, whether in vitro or in vivo is highly valuable. Respirometers sense oxygen levels using porphyrin-based phosphors that get quenched by oxygen or via amperometric oxygen sensors that rely on the generation of an electric current proportional to oxygen pressure. Clark electrode falls into the latter category and has been used extensively in literature, especia.......

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Disclosures

The authors have nothing to disclose.

Acknowledgements

The authors would like to acknowledge Dr. Kevin Bittman for his guidance in establishing the Seahorse XFp in the lab. National Institutes of Health grant GM088213 supported this work.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
100 mm, 60 mm Petri dishesKord-Valmark Labware Products2900, 2901
1.5 mL centrifuge tubesGlobe Scientific6285
15 mL conical tubesCorning430791
22 × 22 mm coverslipGlobe Scientific1404-10
50 mL conical tubesCorning430829
AgarFisher ScientificBP1423-2
Bacto peptoneBD, Bacto211677
Bacto tryptoneBD, Bacto211705
Bacto yeast extractBD, Bacto212705
BleachGeneric
Calcium chloride dihydrate (CaCl2·2H2O)Fisher ScientificC79-500
Carbonyl cyanide 4-(trifluoromethoxy)phenylhydrazone (FCCP)Abcamab120081
CholesterolFisher ScientificC314-500
Deionized water (dH2O)
Dimethyl sulfoxide (DMSO)Thomas ScientificC987Y85
Glass Pasteur pipettesKrackeler Scientific6-72050-900
Magnesium sulfate heptahydrate (MgSO4·7H2O)Fisher ScientificBP213-1
Potassium phosphate dibasic (K2HPO4)Fisher ScientificBP363-1
Potassium phosphate monobasic (KH2PO4)Fisher ScientificP285-500
Sodium chlorideFisher ScientificBP358-10
Sodium hydroxide (NaOH)Fisher ScientificBP359-500
Sodium phosphate dibasic anhydrous (Na2HPO4)Fisher ScientificBP332-1
Seahorse XFp AnalyzerAgilent
Seahorse XFp FluxPakAgilent103022-100
Sodium AzideSigma-AldrichS2002

References

  1. Nelson, D. L., Cox, M. M. Ch. 19. Lehninger Principles of Biochemistry. Ahr, K. , W. H. Freeman and Company. 707-772 (2008).
  2. Marchi, S., et al. Mitochondrial and endoplasmic reticulum calcium homeostasis and cell death. Cell Calcium. 69, 62-72 (2018).
  3. Sarasija, S., et al.

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