PROSTAGLANDIN E(2) ALTERS TERMINAL GLYCOSYLATION OF HIGH-MOLECULAR-WEIGHT GLYCOPROTEINS, RELEASED BY PIG GASTRIC MUCOUS CELLS IN-VITRO

被引:15
作者
ENSS, ML
SCHMIDTWITTIG, U
HEIM, HK
SEWING, KF
机构
[1] HANNOVER MED SCH,ANIM FACIL,D-30623 HANNOVER,GERMANY
[2] HANNOVER MED SCH,INST GEN PHARMACOL,D-30623 HANNOVER,GERMANY
来源
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS | 1995年 / 52卷 / 05期
关键词
D O I
10.1016/0952-3278(95)90035-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The gastric mucus layer consists of high molecular weight glycoproteins (HMG). E-Type prostaglandins (PGs) stimulate total HMG release from isolated gastric mucous cells, We determined the effects of PGE(2) on HMG glycosylation. Pig gastric mucous cells were cultured for 20 h with 1 mu mol/l PGE(2). Released HMG were isolated by gel chromatography and periodic acid-Schiff (PAS)-positive sugars and protein-bound [C-14]GlcNAc were determined, Monosaccharides terminally linked to HMG oligosaccharide chains were monitored by lectin enzyme linked immunosorbent assay (ELISA): N-acetylglucosamine (GlcNAc) with Datura stramonium agglutinin, N-acetylgalactosamine (GalNAc) with soy bean agglutinin, fucose (Fuc) with Ulex europaeus I agglutinin and sialic acids (Sial) with Sambucus nigra agglutinin. PGE(2) stimulated total HMG release, indicated by an increase of PAS-positive sugars to 170% and [C-14]GlcNAc to 220% of controls, Terminal GlcNAc increased to 128%, GalNAc to 133%, Fuc to 165% and Sial to 182%. In addition to stimulation of total HMG release, PGE, caused alterations of HMG glycosylation, which may modulate HMG viscosity and microbiological barrier function.
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页码:333 / 340
页数:8
相关论文
共 47 条
[1]  
ALLEN A, 1990, CELL BIOL INFLAMMATI, P113
[2]  
BADDOUR LM, 1990, PRINCIPLES PRACTICE, P9
[3]  
BERSIMBAEV RI, 1993, CELLULAR MECHANISMS, P173
[4]   INHIBITION OF ADHESION OF ESCHERICHIA-COLI K88 TO PIGLET ILEAL MUCUS BY LACTOBACILLUS SPP [J].
BLOMBERG, L ;
HENRIKSSON, A ;
CONWAY, PL .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1993, 59 (01) :34-39
[5]  
BOLAND CR, 1986, CANCER RES, V46, P5724
[6]  
CARLSTEDT I, 1985, ESSAYS BIOCHEM, V20, P40
[7]   TERMINAL GLYCOSYLATION IN HUMAN CERVICAL MUCIN [J].
CHANTLER, EN ;
SCUDDER, PR .
CIBA FOUNDATION SYMPOSIA, 1984, 109 :180-195
[8]   PURIFICATION AND CHARACTERIZATION OF A PEANUT-AGGLUTININ-BINDING PANCREATIC-CANCER-RELATED SERUM MUCUS GLYCOPROTEIN [J].
CHING, CK ;
RHODES, JM .
INTERNATIONAL JOURNAL OF CANCER, 1990, 45 (06) :1022-1027
[9]  
COHEN PS, 1991, MOL PATHOGENESIS GAS, P29
[10]   MUCIN DEGRADATION IN THE HUMAN COLON - PRODUCTION OF SIALIDASE, SIALATE O-ACETYLESTERASE, N-ACETYLNEURAMINATE LYASE, ARYLESTERASE, AND GLYCOSULFATASE ACTIVITIES BY STRAINS OF FECAL BACTERIA [J].
CORFIELD, AP ;
WAGNER, SA ;
CLAMP, JR ;
KRIARIS, MS ;
HOSKINS, LC .
INFECTION AND IMMUNITY, 1992, 60 (10) :3971-3978