The specific goals of the proposed research are: to detemine the content and composition of lipids in the undegraded mucus glycoprotein isolated from gastric mucus; to establish the requirements of glyceroglucolipids for for interacting with mucus glycoprotein, and to determine whether this interaction involves the protein or carbohydrate component of the glycoprotein; to provide the information as to the topography of lipids within the undegraded gastric mucus glycoprotein polymer; to determine whether glyceroglucolipids protect the mucus glycoprotein polymer from the degradation by pepsin; to determine the effect of lipids on the rheological properties of mucus glycoprotein, and J to evaluate the role of mucus lipids in the process of H+ retardation by gastric mucus; to determine whether activities of enzymes involved in the biosynthesis of glyceroglucolipids in gastric mucosa of patients with gastric diseases differ from that of normals. The undegraded mucus glycoproteins, isolated from pig, dog and rat gastric mucus by the equilibrium centrifugation in CsCl density gradient, will be used to study the content and composition of lipids. Dissociation of the undegraded mucus glycoproteins into a central protein component and the reduced glycoprotein monomers will be performed by the reductive cleavage of dissulfide bridges. The effect of lipids on the peptic digestion of mucus glycoprotein will be measured by the trinitrophenylation method. Viscosity measurements and the study on the role of lipids in the retardation of H+ diffusion by gastric mucus will be performed on the intact and delipidated mucus and glycoprotein. Human gastric mucosal biopsy specimens will be used to study the activities of enzymes involved in the biosynthesis of glyceroglucolipids.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK021684-09
Application #
3227080
Study Section
(GCN)
Project Start
1978-09-15
Project End
1987-08-31
Budget Start
1986-09-01
Budget End
1987-08-31
Support Year
9
Fiscal Year
1986
Total Cost
Indirect Cost
Name
New York Medical College
Department
Type
Schools of Medicine
DUNS #
City
Valhalla
State
NY
Country
United States
Zip Code
10595
Slomiany, A; Grabska, M; Slomiany, B A et al. (1993) Intracellular transport, organelle biogenesis and establishment of Golgi identity: impact of brefeldin A on the activity of lipid synthesizing enzymes. Int J Biochem 25:891-901
Zirvi, K A; Najjar, T A; Slomiany, B L (1993) Sensitivity of human colon tumor metastases to anticancer drugs in athymic (nude) mice. Cancer Lett 72:39-44
Zirvi, K A; Keogh, J P; Slomiany, A et al. (1993) Effects of exogenous transglutaminase on spreading of human colorectal carcinoma cells. Cancer Biochem Biophys 13:283-94
Keogh, J P; Zirvi, K A; Vossough, S et al. (1993) Pharmacological alterations of cellular transglutaminase activity and invasiveness in human colorectal carcinoma cells. Cancer Biochem Biophys 13:209-20
Liu, J; Fekete, Z; Slomiany, A et al. (1993) Activation of gastric mucosal calcium channels by epidermal growth factor. Int J Biochem 25:29-35
Slomiany, B L; Slomiany, A (1992) Mechanism of Helicobacter pylori pathogenesis: focus on mucus. J Clin Gastroenterol 14 Suppl 1:S114-21
Sundaram, P; Slomiany, B L; Slomiany, A et al. (1992) Tyrosylprotein sulfotransferase activity is increased in human gastric mucosa of alcoholics. Am J Gastroenterol 87:1460-3
Slomiany, B L; Liu, J; Fekete, Z et al. (1992) Modulation of gastric mucosal calcium channels activity by platelet-derived growth factor. J Physiol Pharmacol 43:333-44
Slomiany, A; Grzelinska, E; Grabska, M et al. (1992) Intracellular processes associated with glycoprotein transport and processing. Arch Biochem Biophys 298:167-75
Slomiany, B L; Piotrowski, J; Mojtahed, H et al. (1992) Ebrotidine effect on the proteolytic and lipolytic activities of Helicobacter pylori. Gen Pharmacol 23:203-6

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