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PMID: 7525398 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

The level of the zymogen granule protein GP2 is elevated in a rat model for acute pancreatitis.

Gastroenterology ·Vol. 107 ·No. 6 ·1994-12-00 ·Pages 1819-27

Lowe AW, Luthen RE, Wong SM, Grendell JH

Abstract

GP2 is the major membrane protein in pancreatic zymogen granules. It is linked to the membrane via a glycosyl-phosphatidylinositol linkage. After cleavage, a significant fraction of GP2 becomes soluble. The present study assessed whether GP2 is a useful serum marker for acute pancreatitis. Using an anti-GP2 monoclonal antibody, an enzyme-linked immunosorbent assay was developed to measure the serum levels of GP2 in rats with cerulein-induced acute pancreatitis. The anti-GP2 antibody was specific because it did not cross-react with uromodulin, a structurally similar protein to GP2, or to protein extracts from nonpancreatic tissues. Eight hours after the induction of pancreatitis, the serum levels of amylase, lipase, and GP2 peaked. Peak GP2 levels were 4.2 times higher than those of controls. At 24 hours, GP2 was still 70% of the peak level, whereas amylase and lipase were 5.5% and 0.5%, respectively, of their peak levels. GP2 may serve as a potentially valuable marker for clinical acute pancreatitis.

MeSH Terms
Acute Disease Amylases/blood Animals Biomarkers/blood Cytoplasmic Granules/metabolism Disease Models, Animal Enzyme Precursors/metabolism Enzyme-Linked Immunosorbent Assay GPI-Linked Proteins Lipase/blood Membrane Glycoproteins/blood Pancreas/enzymology,metabolism Pancreatitis/blood,diagnosis,enzymology Rats
Chemicals
Biomarkers Enzyme Precursors GPI-Linked Proteins Gp2 protein, rat Membrane Glycoproteins Lipase Amylases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Lowe A W
Department of Medicine, Stanford University School of Medicine, California.
Luthen R E
Wong S M
Grendell J H
Article Info
Journal
Gastroenterology
Abbr.
Gastroenterology
ISSN
0016-5085
Published
1994-12-00
Pages
1819-27
Language
English
Region
United States
NLM ID
0374630
Subset
IM
Grants
NIDDK NIH HHS · DK38707 · United States
NIDDK NIH HHS · DK43294-01 · United States
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