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Isolation of Rat Liver Hepatocytes

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Book cover Basic Cell Culture Protocols

Part of the book series: Methods in Molecular Biology™ ((MIMB,volume 75))

Abstract

The liver is composed of hepatocytes, endothelial, Kupffer, fat-storing, and pit cells. This chapter describes a technique for isolating hepatocytes, which represent 60–65% of the cells of the liver and about 80% of the volume of the organ (since they are larger than the other cells) (13). Two years after Howard et. al. (4) discovered that collagenase was a very important tool in the separation of liver cells, Berry and Friend (5) introduced the technique of collagenase perfusion of the liver.

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References

  1. Weibel, E. R., Staubli, W., Gnagi, H. R., and Hess, F. A. (1969) Correlated morphometric and biochemical studies on the liver. I. Morphometric model, stereologic methods, and normal morphometric data for rat liver. J. Cell Biol. 42, 68–91.

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  6. Berry, M. N., Edwards, A. M., and Barritt, G. J. (1991) Isolated hepatocytes preparation, properties and applications, in Laboratory Techniques in Biochemistry and Molecular Biology, vol. 21 (Burdon, R. H., and von Knippersberg, P. H., eds.), Elsevier, Amsterdam, New York, Oxford.

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© 1997 Humana Press Inc., Totowa, NJ

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Neufeld, D.S. (1997). Isolation of Rat Liver Hepatocytes. In: Pollard, J.W., Walker, J.M. (eds) Basic Cell Culture Protocols. Methods in Molecular Biology™, vol 75. Humana Press, Totowa, NJ. https://doi.org/10.1385/0-89603-441-0:145

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  • DOI: https://doi.org/10.1385/0-89603-441-0:145

  • Publisher Name: Humana Press, Totowa, NJ

  • Print ISBN: 978-0-89603-441-9

  • Online ISBN: 978-1-59259-561-7

  • eBook Packages: Springer Protocols

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