Distribution of glycosyltransferases among Golgi apparatus subfractions from liver and hepatomas of the rat

• Published in: Biochimica et biophysica acta Vol. 1115; no. 2; pp. 108 - 122
• Main Authors: Hartel-Schenk, Sabine, Minnifield, Nita, Reutter, Werner, Hanski, Christoph, Bauer, Christian, James Morré, D.
• Format: Journal Article
• Language: English
• Published: Amsterdam Elsevier B.V 06.12.1991; Elsevier
• Subjects: Analytical, structural and metabolic biochemistry; Animals; Biological and medical sciences; Cell Membrane - enzymology; Dipeptidyl Peptidase 4; Dipeptidyl-Peptidases and Tripeptidyl-Peptidases - metabolism; Endoplasmic Reticulum - enzymology; Endoplasmic Reticulum - ultrastructure; Enzymes and enzyme inhibitors; Fucosyltransferases - metabolism; Fundamental and applied biological sciences. Psychology; Glycosyltransferase; Glycosyltransferases - metabolism; Golgi apparatus; Golgi Apparatus - enzymology; Hepatoma; Liver; Liver - enzymology; Liver - ultrastructure; Liver Neoplasms, Experimental - enzymology; Liver Neoplasms, Experimental - ultrastructure; Male; Microscopy, Electron; Rat; Rats; Rats, Inbred F344; Tissue Distribution; Transferases; ST; Rat; Glycosyltransferase; Liver; Hepatoma; GT; FT; Golgi apparatus; RLT; DPP IV; 6-FT; 2-FT; GlcNAcT; Enzyme; Rodentia; Glycosylation; Glycoconjugate; Electron microscopy; Vertebrata; Mammalia; Enzymatic activity; Liver cell carcinoma; Tumor
• ISSN: 0304-4165; 0006-3002; 1872-8006
• DOI: 10.1016/0304-4165(91)90019-D

Glycosyltransferase activities of highly purified fractions of Golgi apparatus, plasma membrane and endoplasmic reticulum, all from the same homogenates, were analyzed and compared. Additionally, Golgi apparatus were unstacked and the individual cisternae separated into fractions enriched in cis, median and trans elements using the technique of preparative free-flow electrophoresis. Golgi apparatus from both liver and hepatomas were enriched in all glycosyltransferases compared to endoplasmic reticulum and plasma membranes. However, Golgi apparatus from hepatomas showed both elevated fucosyltransferase and galactosyltransferase activities but reduced sialyltransferase and dipeptidyl peptidase IV (DPP IV) activities compared to liver. Activity of N-acetylglucos-aminyltransferase was approximately the same in both liver and hepatoma Golgi apparatus. With normal liver, sialyl- and galactosyltransferase activities and DPP IV showed a marked cis-to- trans gradient of activity. Fucosyl-transferase was concentrated in two regions of the electrophoretic separations, one corresponding to cis cisternae and one corresponding to trans cisternae. N-Acetylglucosaminyltransferase activity was more widely distributed but the endogenous acceptor activity was predominantly cis. With hepatoma Golgi apparatus, the pattern for DPP IV was similar to that for liver but those of sialyl- and galactosyltransferases decreased. For fucosyltransferases, activity dependent on exogenous acceptor was medial whereas with endogenous acce9tor, two activity peaks, cis and trans, still were observed. For N-acetylglucosaminyltransferase the pattern for hepatoma was similar to that for liver. The results indicate alterations in the distribution of glycosyltransferase activities within the Golgi apparatus in hepatotumorigenesis that may reflect altered cell surface glycosylation patterns.