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1Department of Molecular Medicine,Sapienza University, 2Department of Internal Medicine – DMISM,Sapienza University, 3Center for Life Nano Science@Sapienza,Istituto Italiano di Tecnologia, 4Pasteur Institute Italy-Fondazione Cenci Bolognetti, 5INSERM U1052-Cancer Research Center of Lyon, 6Department of Hepatology,Croix Rousse Hospital, Hospices Civils de Lyon
Capitoli
- 00:04Titolo
- 00:32Thawing, Amplification, and Cryopreservation of HepaRG Cells
- 02:20Differentiation of HepaRG cells (Day 0 21) and Induction of Vesicular Steatosis (Day 21 26)
- 04:25Evaluation of Lipid Overloading and Steatosis Induction: Oil Red O Staining
- 06:04Evaluation of Lipid Overloading and Steatosis Induction: Bodipy Staining
- 07:02Results: Induction and Quantification of Vesicular Steatosis in HepaRG Cells
- 08:34Conclusion
In this study, we describe a detailed protocol for inducing liver vesicular steatosis in differentiated HepaRG cells with the fatty acid salt sodium oleate and employ methods for detection and quantification of lipid accumulation, including coherent anti-Stokes Raman scattering (CARS) microscopy, cytofluorimetric analysis, Oil red O staining, and qPCR.
