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PMID: 6796063 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Effect of cycloheximide, beta-D-xylosides and beta-D-galactosides on heparin biosynthesis in mouse mastocytoma.

The Biochemical journal ·Vol. 194 ·No. 2 ·1981-02-15 ·Pages 575-86

Robinson HC, Lindahl U

Abstract

Heparin biosynthesis has been investigated with mouse mastocytoma in vitro. Minced tumour tissue catalysed the incorporation of [35S]sulphate and [3H]glucosamine into heparin and to a smaller extent into chondroitin sulphate. Addition of cycloheximide caused an inhibition (greater than 80%) of incorporation of each labelled precursor into both polysaccharides. Addition of benzyl beta-D-xyloside relieved the inhibition of incorporation into chondroitin sulphate and restored it to more than threefold that of the control incubation. The effect of beta-D-xyloside on incorporation into heparin was less marked although a consistent small increase of incorporation into this polysaccharide was observed. beta-D-Xyloside did, however, cause a marked incorporation of 35S and 3H labels into material of low molecular weight, which appeared to comprise heparin-like fragments. It is proposed that these fragments arise through a breakdown of the usual process of heparin biosynthesis.

MeSH Terms
Animals Chondroitin Sulfates/biosynthesis Chromatography, Gel Chromatography, Ion Exchange Cycloheximide/pharmacology Galactosides/pharmacology Glycosaminoglycans/biosynthesis Glycosides/pharmacology Heparin/biosynthesis In Vitro Techniques Mast-Cell Sarcoma/metabolism Mice Xylose/analogs & derivatives,pharmacology
Chemicals
Galactosides Glycosaminoglycans Glycosides xylosides Heparin Chondroitin Sulfates Cycloheximide Xylose
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Robinson H C
Lindahl U
References (21)
21 references, click to expand
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Article Info
Journal
The Biochemical journal
Abbr.
Biochem J
ISSN
0264-6021
Published
1981-02-15
Pages
575-86
Language
English
Region
England
NLM ID
2984726R
PMCID
PMC1162782
Subset
IM
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