Literature DB >> 8515054

Effects of digitonin on the intracellular content of rat hepatocytes: implications for its use in the study of intralobular heterogeneity.

L Racine1, J Y Scoazec, A Moreau, D Bernuau, G Feldmann.   

Abstract

Anterograde or retrograde perfusion of rat liver with digitonin selectively permeabilizes the periportal or the perivenous zone of the hepatic lobule. Digitonin perfusion is used to analyze the effluents released by permeabilized hepatocytes or, combined with collagenase perfusion, to obtain cell suspensions enriched in either periportal or perivenous hepatocytes. Despite the wide use of digitonin to study lobular heterogeneity, its affects on rat hepatocytes are not well documented. We therefore analyzed the effects of digitonin perfusion on the intracellular content of rat hepatocytes by combining electron microscopy, histoenzymology, immunohistochemistry, and in situ hybridization. At the concentration currently used for the study of lobular heterogeneity, digitonin perfusion induced a marked cytosolic clarification of permeabilized hepatocytes, while most organelles except mitochondria were well preserved. In the digitonin-altered zones, there was no histochemical detection of non-membrane-bound enzymes (lactate dehydrogenase, glutamate dehydrogenase), whereas membrane-bound enzymes (succinate dehydrogenase, beta-hydroxybutyrate dehydrogenase, NADPH dehydrogenase, glucose-6-phosphatase) were still detected. Immunohistochemistry and in situ hybridization revealed significant amounts of several plasma proteins (albumin, alpha 2-macroglobulin, alpha 1-inhibitor 3, alpha 1-acid glycoprotein) and their respective mRNAs in digitonin-permeabilized hepatocytes. The demonstration that digitonin-permeabilized hepatocytes retain many intracellular constituents shows that biochemical analysis of cellular effluents released from digitonin-permeabilized hepatocytes must be interpreted with caution and that the apparent characteristics of cell suspensions obtained by the digitonin-collagenase technique might be significantly altered by contamination with permeabilized hepatocytes from the opposite zone.

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Year:  1993        PMID: 8515054     DOI: 10.1177/41.7.8515054

Source DB:  PubMed          Journal:  J Histochem Cytochem        ISSN: 0022-1554            Impact factor:   2.479


  6 in total

1.  Hepatic intralobular mapping of fructose metabolism in the rat liver.

Authors:  S P Burns; H C Murphy; R A Iles; R A Bailey; R D Cohen
Journal:  Biochem J       Date:  2000-07-15       Impact factor: 3.857

2.  Gluconeogenesis, glucose handling, and structural changes in livers of the adult offspring of rats partially deprived of protein during pregnancy and lactation.

Authors:  S P Burns; M Desai; R D Cohen; C N Hales; R A Iles; J P Germain; T C Going; R A Bailey
Journal:  J Clin Invest       Date:  1997-10-01       Impact factor: 14.808

3.  A method for determination in situ of variations within the hepatic lobule of hepatocyte function and metabolite concentrations.

Authors:  S P Burns; R D Cohen; R A Iles; J P Germain; T C Going; S J Evans; P Royston
Journal:  Biochem J       Date:  1996-10-15       Impact factor: 3.857

4.  Distribution of albumin, alpha 1-inhibitor 3 and their respective mRNAs in periportal and perivenous rat hepatocytes isolated by the digitonin-collagenase technique.

Authors:  L Racine; J Y Scoazec; A Moreau; P Chassagne; D Bernuau; G Feldmann
Journal:  Biochem J       Date:  1995-01-01       Impact factor: 3.857

5.  Subpopulations of rat hepatocytes separated by Percoll density-gradient centrifugation show characteristics consistent with different acinar locations.

Authors:  J C Osypiw; R L Allen; D Billington
Journal:  Biochem J       Date:  1994-12-01       Impact factor: 3.857

6.  Zonation of gluconeogenesis, ketogenesis and intracellular pH in livers from normal and diabetic ketoacidotic rats: evidence for intralobular redistribution of metabolic events in ketoacidosis.

Authors:  S P Burns; R D Cohen; R A Iles; R A Bailey; M Desai; J P Germain; T C Going
Journal:  Biochem J       Date:  1999-10-01       Impact factor: 3.857

  6 in total

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