Caerulein-induced trypsinogen activation and acinar cell injury in different murine strains

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Show simple item record Champion, Thomas 2006-07-06T17:11:43Z 2006-07-06T17:11:43Z 2006-07-06T17:11:43Z
dc.description Molecular & Cell Biology III Room G027 Dykes 3:00 PM Abstract 187 en
dc.description.abstract Acute pancreatitis is an inflammatory disorder of the pancreas. Most progress in research of its pathogenesis was obtained from experimental models in rats and mice. In the initial onset, trypsinogen activation plays a critical role. Proteomic studies of exocrine pancreatic tissue revealed differences in trypsinogen isoform patterns of various mouse strains. In the present study, we asked what is the extent of trypsinogen activation, if any, in caerulein-hyperstimulated pancreatic acini prepared from four different mouse strains. The strains used were CD1 and NMRI, which are vigorously outbred, and C57BL/6 and FVB, which are inbred. The pancreatic acini were isolated from the pancreata using collagenase digestion. Acini were stimulated with 0.1µM caerulein. Trypsin activity was fluorometrically measured with the fluorogenic substrate BZiPAR (Molecular Probes/USA). Protein concentration in acini homogenates was estimated by Bradford. Cell injury in acini suspensions was quantified based on measurement of lactate dehydrogenase (LDH) activity with the Cytotoxicity Detection Kit (Roche/Germany). C57BL/6 showed four to five times higher trypsin activation than the other three strains, although initial trypsinogen content was not statistically different. Cell injury measured by LDH release, does not correlate with the levels of trypsin activity. Higher trypsin activity in caerulein hyperstimulated acini of C57BL/6 is accompanied by an increased Cathepsin B activitiy. Different levels of trypsinogen activation in various strains might be caused by different quantities of various trypsinogen isoforms in mouse strains, different activities of trypsinogen-activation enzymes (such as Cathepsin B), and/or various levels of trypsin inhibitors. Future studies will focus on these questions. en
dc.description.sponsorship Halangk, Walter Surgery, Magdeburg, Germany en
dc.format.extent 1605632 bytes
dc.format.mimetype application/
dc.language.iso en_US en
dc.subject acute pancreatitis onset en
dc.title Caerulein-induced trypsinogen activation and acinar cell injury in different murine strains en
dc.type Presentation en

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