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Role of Cathepsin B in Intracellular Trypsinogen Activation and the Onset of Acute Pancreatitis

Overview
Journal J Clin Invest
Specialty General Medicine
Date 2000 Sep 21
PMID 10995788
Citations 221
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Abstract

Autodigestion of the pancreas by its own prematurely activated digestive proteases is thought to be an important event in the onset of acute pancreatitis. The mechanism responsible for the intrapancreatic activation of digestive zymogens is unknown, but a recent hypothesis predicts that a redistribution of lysosomal cathepsin B (CTSB) into a zymogen-containing subcellular compartment triggers this event. To test this hypothesis, we used CTSB-deficient mice in which the ctsb gene had been deleted by targeted disruption. After induction of experimental secretagogue-induced pancreatitis, the trypsin activity in the pancreas of ctsb(-/-) animals was more than 80% lower than in ctsb(+/+) animals. Pancreatic damage as indicated by serum activities of amylase and lipase, or by the extent of acinar tissue necrosis, was 50% lower in ctsb(-/-) animals. These experiments provide the first conclusive evidence to our knowledge that cathepsin B plays a role in intrapancreatic trypsinogen activation and the onset of acute pancreatitis.

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References
1.
Lerch M, Saluja A, Runzi M, Dawra R, Steer M . Luminal endocytosis and intracellular targeting by acinar cells during early biliary pancreatitis in the opossum. J Clin Invest. 1995; 95(5):2222-31. PMC: 295834. DOI: 10.1172/JCI117912. View

2.
Saluja A, Hashimoto S, Saluja M, Powers R, Meldolesi J, Steer M . Subcellular redistribution of lysosomal enzymes during caerulein-induced pancreatitis. Am J Physiol. 1987; 253(4 Pt 1):G508-16. DOI: 10.1152/ajpgi.1987.253.4.G508. View

3.
Niederau C, Ferrell L, Grendell J . Caerulein-induced acute necrotizing pancreatitis in mice: protective effects of proglumide, benzotript, and secretin. Gastroenterology. 1985; 88(5 Pt 1):1192-204. DOI: 10.1016/s0016-5085(85)80079-2. View

4.
FIGARELLA C, Barrett A . Possible lysosomal activation of pancreatic zymogens. Activation of both human trypsinogens by cathepsin B and spontaneous acid. Activation of human trypsinogen 1. Biol Chem Hoppe Seyler. 1988; 369 Suppl:293-8. View

5.
Gorelick F, Modlin I, Leach S, Carangelo R, Katz M . Intracellular proteolysis of pancreatic zymogens. Yale J Biol Med. 1992; 65(5):407-20; discussion 437-40. PMC: 2589730. View