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PMID: 1527047 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Oligosaccharide structures of mucins secreted by the human colonic cancer cell line CL.16E.

The Journal of biological chemistry ·Vol. 267 ·No. 27 ·1992-09-25 ·Pages 19248-57

Capon C, Laboisse CL, Wieruszeski JM, Maoret JJ, Augeron C, Fournet B

Abstract

Cl.16E, a stably differentiated clonal derivative of the human colonic cancer cell line HT29, was used to investigate the structure of oligosaccharide chains of mucins in colonic cancer. Secretory mucins were purified by equilibrium density gradient centrifugation in CsCl. Oligosaccharide side chains were isolated after beta-elimination. Compositional analysis of oligosaccharide-alditols performed after purification by gel filtration on a Bio-gel P-6 column showed 1) that GalNAc residues were located exclusively at the reducing ends of the chains, and 2) that fucose was absent from the preparation. Oligosaccharide-alditols were separated by high performance liquid chromatography (HPLC) on quaternary amine packings into a minor neutral fraction representing about 6.5% by weight of released oligosaccharides and four acidic fractions. Two acidic fractions, namely FI and FII encompassing mono- and disialylated structures, respectively, and containing 78% of total oligosaccharide alditols, were separated by HPLC. Structural determinations were carried out using methylation analysis, 1H NMR spectroscopy, and fast atom bombardment-mass spectrometry. Twelve oligosaccharide structures were determined which ranged in size from 3 to 8 residues. These oligosaccharides were based on core types 1, 2, and 4. Elongation of oligosaccharide chains was terminated by addition of sialic acid in alpha 2-3 linkage to Gal beta 1-3R and to Gal beta 1-4R residues. The predominant structure was a hexasaccharide (fraction FII-4). This contrasts with normal colonic mucins whose oligosaccharides were previously found to be based on core 3 structures and carry sialic acids in alpha (2-6) linkage to Gal beta 1-3R, to Gal beta 1-4R, and to GalNAc alpha-R (Podolsky, D.K. (1985) J. Biol. Chem. 260, 8262-8271; Podolsky, D.K. (1985) J. Biol. Chem. 260, 15510-15515). Collectively our findings suggest that Cl.16E colon cancer cells are able to synthesize mucin oligosaccharides of gastric type whose elongation is truncated by premature sialylation.

MeSH Terms
Adenocarcinoma/chemistry Carbohydrate Sequence Colonic Neoplasms/chemistry Humans In Vitro Techniques Magnetic Resonance Spectroscopy Mass Spectrometry Molecular Sequence Data Mucins/chemistry Oligosaccharides/chemistry Tumor Cells, Cultured
Chemicals
Mucins Oligosaccharides
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Capon C
Laboratoire de Chimie Biologique de l'USTL, Unité Mixte de Recherche du Centre National de la Recherche Scientifique, Villeneuve d'Ascq, France.
Laboisse C L
Wieruszeski J M
Maoret J J
Augeron C
Fournet B
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1992-09-25
Pages
19248-57
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
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