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Method Article

Measurement of Fatty Acid β-Oxidation in a Suspension of Freshly Isolated Mouse Hepatocytes

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DOI:

10.3791/62904

September 9th, 2021

* These authors contributed equally

In This Article

Summary

Fatty acid β-oxidation is an essential metabolic pathway responsible for generating energy in many different cell types, including hepatocytes. Here, we describe a method to measure fatty acid β-oxidation in freshly isolated primary hepatocytes using 14C-labeled palmitic acid.

Abstract

Fatty acid β-oxidation is a key metabolic pathway to meet the energy demands of the liver and provide substrates and cofactors for additional processes, such as ketogenesis and gluconeogenesis, which are essential to maintain whole-body glucose homeostasis and support extra-hepatic organ function in the fasted state. Fatty acid β-oxidation occurs within the mitochondria and peroxisomes and is regulated through multiple mechanisms, including the uptake and activation of fatty acids, enzyme expression levels, and availability of cofactors such as coenzyme A and NAD+. In assays that measure fatty acid β-oxidation in liver homogenates, cell lysis and the common addition of supraphysiological levels of cofactors mask the effects of these regulatory mechanisms. Furthermore, the integrity of the organelles in the homogenates is hard to control and can vary significantly between preparations. The measurement of fatty acid β-oxidation in intact primary hepatocytes overcomes the above pitfalls. This protocol describes a method for the measurement of fatty acid β-oxidation in a suspension of freshly isolated primary mouse hepatocytes incubated with 14C-labeled palmitic acid. By avoiding hours to days of culture, this method has the advantage of better preserving the protein expression levels and metabolic pathway activity of the original liver, including the activation of fatty acid β-oxidation observed in hepatocytes isolated from fasted mice compared to fed mice.

Introduction

Fatty acid β-oxidation is an essential process in lipid metabolism, providing a catabolic pathway to balance fatty acid synthesis and intake from the diet. This process generates energy for multiple organs, including the cardiac muscle, kidney cortex, and fasted liver, and utilizes fatty acids obtained from the diet, adipose tissue lipolysis, and internal triglyceride stores1,2.

Oxidation of fatty acid through the β-oxidation pathway results in the sequential shortening of the fatty acyl chain by two carbons at a time, released as acetyl-CoA, and this process occurs both i....

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Protocol

All experimental procedures on mice (C57BL/6J, males, 9-11 weeks of age) were approved by the Institutional Animal Care and Use Committees (IACUC) of West Virginia University.

1. Hepatocyte isolation

  1. Preparation
    1. In the days before the hepatocyte isolation, prepare the buffers and cell culture media listed in Table 1. Set up a water bath with the temperature set to 37 °C close to where the surgery will be performed.
    2. On the day of the hepatocyte isolation, under a laminar flow hood, transfer 35 mL of Buffer 1 to a sterile 50 mL centrifuge tube and 70 mL of Buffer 2 to a 100 mL sterile beaker....

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Results

The liver perfusion described here typically yields 30-40 million cells/liver with average viability of 80%, as estimated by trypan blue exclusion (Figure 2). The typical concentration of glucose in the Krebs-Henseleit buffer (KHB), which is used to prepare the perfusion Buffers 1 and 2, is 11 mM. When measuring fatty acid β-oxidation in hepatocytes isolated from fasted mice, the concentration of glucose in the KHB can be lowered to better represent the fasted state. As shown in

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Discussion

During the liver perfusion, it is critical to avoid the introduction of air bubbles, as they block the microcapillaries in the liver, preventing or restricting the buffer circulation and overall decreasing the hepatocyte yield and viability20,21. Precautions, such as closely inspecting the buffer-filled inlet line before cannulation of the IVC and avoiding lifting the inlet line off the tube containing Buffer 1 to switch to Buffer 2, as described herein, can succ.......

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Disclosures

The authors have no conflicts of interest to disclose.

Acknowledgements

This work was supported by the National Institutes of Health grant R35GM119528 to Roberta Leonardi.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
(R)-(+)-Etomoxir sodium saltTocris Bioscience4539/10
[1-14C]-Palmitic acid, 50–60 mCi/mmol, 0.5 mCi/mLAmerican Radiolabeled ChemicalsARC 0172A
1 M HEPES, sterileCorning25060CI
10 µL disposable capillaries/pistons for positive displacement pipetteMettler Toledo17008604
1000 µL, 200 µL, and 10 µL pipettes and tips
5 mL, 10 mL, and 25 mL serological pipettes
50 mL sterile centrifuge tubesCellTreat229421
70% Perchloric acidFisher ScientificA2296-1LB
BSA, fatty acid-freeFisher ScientificBP9704100
CaCl2 dihydrateMilliporeSigma223506
D-(+)-GlucoseMilliporeSigmaG7021
EGTAGold BiotechnologyE-217
EthanolPharmco111000200CSPP
Filter System, 0.22 μm PES Filter, 500 mL, SterileCellTreat229707
Gentamicin sulphateGold BiotechnologyG-400-25
HDPE, 6.5 mL scintillation vialsFisher Scientific03-342-3
Hemocytometer
Hypodermic needles 22 G, 1.5 inBD Biosciences305156
IsofluraneVetOne502017
KClFisher ScientificBP366-1
KH2PO4MilliporeSigmaP5655
Liberase TM Research GradeMilliporeSigma5401119001Defined blend of purified collagenase I and II with a medium concentration of thermolysin
M199 mediumMilliporeSigmaM5017
MgSO4 heptahydrateMilliporeSigmaM1880
MicrocentrifugeFisher ScientificaccuSpin Micro 17
Microdissecting ScissorsRoboz Surgical Instrument CoRS-5980
NaClChem-Impex International30070
NaHCO3Acros Organics424270010
Palmitic acidMilliporeSigmaP0500
Penicillin/streptomycin (100x)Gibco15140122
Phosphate buffered saline (PBS)Cytiva Life SciencesSH30256.01
Positive displacement pipette MR-10, 10 µLMettler Toledo17008575
Refrigerated centrifuge with inserts for 50 mL conical tubesEppendorf5810 R
Round-bottom, 14 mL, polypropylene culture test tubesFisher Scientific14-956-9A
Scintillation counterPerkin ElmerTriCarb 4810 TR
ScintiVerse BD cocktailFisher ScientificSX18-4
Shaking water bath, 30 L capacityNew Brunswick Scientific Model G76
Sterile cell strainers, 100 µmFisher Scientific22363549
Thumb Dressing ForcepsRoboz Surgical Instrument CoRS-8120
Trypan BlueCorning25900CI
Variable-flow peristaltic pumpFisher Scientific138762
Water baths, 2–2.5 L capacity

References

  1. Alves-Bezerra, M., Cohen, D. E. Triglyceride Metabolism in the Liver. Comprehensive Physiology. 8 (1), 1-8 (2017).
  2. Lopaschuk, G. D., Ussher, J. R., Folmes, C. D., Jaswal, J. S., Stanley, W. C. Myocardial fatty acid metabolism in health and disease. Physiological Reviews. 90 (....

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Tags

Beta OxidationHepatocyte SuspensionMitochondrial OxidationPeroxisomal OxidationPalmitic Acid AssayLiver PerfusionRadioactive SubstrateMetabolic Pathways