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In This Article

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

Summary

Primary hepatocytes are a valuable tool to study liver response and metabolism in vitro. Utilizing commercially available reagents, an improved time- and labor-efficient protocol for mouse primary hepatocyte isolation was developed.

Abstract

Primary hepatocytes are used extensively in liver in vitro research, especially in glucose metabolism studies. A base technique has been adapted based on different needs, like time, labor, cost, and primary hepatocyte usage, resulting in various primary hepatocyte isolation protocols. However, the numerous steps and time-consuming reagent preparations in primary hepatocyte isolation are major drawbacks for efficiency. After comparing different protocols for their pros and cons, the advantages of each were combined, and a rapid and efficient primary hepatocyte isolation protocol was formulated. Within only ~35 min, this protocol could yield as much, if not more, healthy primary hepatocytes as other protocols. Further, glucose metabolism experiments performed using the isolated primary hepatocytes validated the usefulness of this protocol in in vitro liver metabolism studies. We also extensively reviewed and analyzed the significance and purpose of each step in this study so that future researchers can further optimize this protocol based on needs.

Introduction

The liver serves as one of the most important organs in the vertebrate body due to the vital role it plays in numerous life-supporting functions like food digestion, blood circulation, and detoxification. Usage of mouse primary hepatocyte in vitro culture is increasingly popular in studies of carbohydrate metabolism and hepatic carcinoma. Therefore, it is important to develop a convenient method for mouse primary hepatocyte isolation while maintaining its innate physiological function. Due to its function as a hub of glucose metabolism, the liver is also central to glucose production and storage1. Experiments with primary hepatocytes <....

Protocol

All procedures were approved by the Johns Hopkins Animal Care and Use Committee. C57BL/6 female mice (8-week old) were used in this study.

1. Preparation:

  1. Mix William's E Medium (GlutaMAX Supplement) with 10% FBS and 1% antibiotic-antimycotic solution to make the culture medium.
  2. Filter 25 mL of collagenase-dispase medium (e.g., Liver Digest Medium) through a 0.45 µm syringe filter to remove particle debris.
  3. Warm 50 mL of double-distille.......

Representative Results

In order to test the efficiency, the present primary hepatocyte isolation protocol was performed on 8-week old female C57BL/6 mice. The attachment and purity of isolated primary hepatocytes were tested. Primary hepatocyte isolation is used for a wide variety of experiments on liver physiology, such as hepatic drug effects and glucose metabolism, pharmaceutical biomarker activity2, insulin sensitivity, and glucose production. Therefore, the activities of the primary hepatocytes isolated with this p.......

Discussion

Various primary hepatocyte isolation protocols have been developed. They also have been kept optimized and adapted based on different needs (Table 1). Isolation protocols are generally composed of two parts: perfusion (including enzyme digestion) and purification.

The perfusion can be performed with the entire liver in vivo2,20,21,22,

Acknowledgements

This work was supported by the National Institutes of Health (Grant 5R01HD095512-02 to S.W.).

....

Materials

NameCompanyCatalog NumberComments
1x PBSGibco10010023
10x HBSSGibco14065-056
12-well PlateFALCON353043Coating not required
6-well PlateFALCON353046Coating not required
anti-AKTCell Signaling2920S
Antibiotic Antimycotic Solution (100x), StabilizedSigma-AldrichA5955
anti-FOXO1Cell Signaling97635S
anti-GAPDHCell Signaling2118S
anti-p-AKT (S473)Cell Signaling9271L
anti-PEPCKSanta CruzSC-166778
anti-p-FOXO1 (S256)Cell Signaling84192S
Cell Strainer, 70 µmCELLTREAT229483
Closed IV Catheter, 24 Gauge 0.75 INBecton Dickinson383511
DMEM, no glucose, no glutamine, no phenol redThermoFisher ScientificA1443001
EnzyChrom Glucose Assay KitBioAssay SystemsEBGL-100
Fetal Bovine Serum (FBS)HycloneSH30071.03
ForskolinMilliporeSigmaF3917-10MG
GlucagonSigma-AldrichG2044
Goat Anti-mouse IgG Secondary AntibodyLI-COR926-68070
Goat Anti-rabbit IgG Secondary AntibodyLI-COR926-32211
GraphPad Prism 8GraphPad SoftwareNA
Hepatocyte Wash MediumGibco17704-024
IBMXCell Signaling13630S
InsulinLillyNDC 0002-8215-01
Ketamine HCL (100 mg/mL)Hospira IncNDC 0409-2051-05
L-GlutamineGibco25030081
Liver Digest MA2:D30ediumGibco17703-034Aliquot within tissue culture hood to 25 mL each in 50 mL tube, and keep in -20 °C freezer
Liver Perfusion MediumGibco17701-038
Pen StrepGibco15140122
PercollGE Healthcare17-0891-01
Peristaltic PumpGilsonMinipuls 2Capable of pumping at 4 mL/min
Petri DishFisherbrand08-757-12
Refrigerated CentrifugeSorvallLegend RTCapable to centrifuge 50 mL tube at 4 °C
Sodium L-LactateSigma-AldrichL7022
Sodium PyruvateGibco11360070
Syringe Filter, PVDF 0.45 µm 30mm diameterCELLTREAT229745
Syringe, 0.5 mLBecton Dickinson329461
Syringe, 60 mLBecton Dickinson309653
Trypan Blue Solution, 0.4%Gibco15250061
Tube, 15 mLCorning430052
Tube, 50 mLCorning430290
Water Bath TankCorningCLS6783Or any water bath tank capable of heating up to 45 °C
William’s E Medium (GlutaMAX Supplement)Gibco32551020
Xylozine (100 mg/mL)Vetone Anased LANDC13985-704-10

References

  1. Han, H. S., Kang, G., Kim, J. S., Choi, B. H., Koo, S. H. Regulation of glucose metabolism from a liver-centric perspective. Experimental and Molecular Medicine. 48, 218 (2016).
  2. Severgnini, M., et al.

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Mouse Primary HepatocytesLiver StudiesGlucose MetabolismHepatic Drug TestingTime efficientLabor efficientProtocolPeristaltic PumpPerfusion MediumCollagenase Dispase MediumWash MediumCell StrainerHBSSCentrifugationCell Culture

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