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Title: Protein tyrosine phosphatase beta, a receptor for Helicobacter pylori vacA toxin. Author: Hirayama T. Journal: Keio J Med; 2002 Dec; 51 Suppl 2():20-3. PubMed ID: 12528931. Abstract: Helicobacter pylori is the leading bacterial cause of food-borne illness worldwide and plays a major role in the development of chronic gastritis, peptic ulcer, and gastric cancer. Strains isolated from patients contain the cagA gene (cytotoxin-associated gene A) and produce the vacuolating cytotoxin VacA. VacA binding to specific high-affinity cell surface receptors was shown by using indirect immunofluorescence and flow cytometry; high-affinity toxin binding was necessary for cell intoxication. A 250-kDa receptor protein tyrosine phosphatase (RPTP) beta served as a receptor for VacA on AZ-521 cells. The overexpression of RPTP beta conferred VacA sensitivity on BHK-21 cells transfected with the RPTP beta cDNA, consistent with RPTP gamma acting as a receptor for VacA. Increased binding of acid- or alkali-activated VacA to RPTP gamma may alter its activity and possibly accelerate or inhibit dephosphorylation of tyrosine on cytosolic proteins. Understanding the pathological responses of wild type and RPTP gamma-deficient animal models may well provide valuable information regarding the mechanism of VacA toxicity.[Abstract] [Full Text] [Related] [New Search]