BackgroundBile acids are the initiating factors of biliary acute pancreatitis. Bile acids can induce the activation of intracellular zymogen, thus leading injury in pancreatic acinar cells. Pathological zymogen activation in pancreatic acinar cells is a common feature of all types of acute pancreatitis. The proteins expressed in pancreatic acinar cells during the activation of zymogen may determine the severity of acute pancreatitis. The present study aims to determine the differentially expressed proteins in taurolithocholic acid 3-sulfate-stimulated pancreatic acinar cells as an in vitro model for acute pancreatitis.MethodsRat pancreatic acinar AR42J cells were treated with taurolithocholic acid 3-sulfate for 20 min. Laser confocal scanning microscopy and flow cytometry were used to detect activated trypsinogen in pancreatic acinar AR42J cells. After the determination of trypsinogen activation, proteome analysis was performed to identify the proteins differentially expressed in taurolithocholic acid 3-sulfate-treated cells and non-treated cells.ResultsAfter treatment with taurolithocholic acid 3-sulfate for 20 min, the activation of trypsinogen in AR42J cells was concurrent with changes in the protein expression profile. Thirty-nine differentially expressed proteins were detected; among these, 23 proteins were up-regulated and 16 proteins were down-regulated. KEGG analysis indicated that these proteins are involved in cellular metabolic pathways, cellular defensive mechanisms, intracellular calcium regulation and cytoskeletal changes.ConclusionThe expression of proteins in the pancreatic acinar cell changes at the early stage of biliary acute pancreatitis. These differentially expressed proteins will provide valuable information to understand the pathophysiologic mechanism biliary acute pancreatitis and may be useful for prognostic indices of acute pancreatitis. 相似文献
A porous ZnCo2O4 micro-rice like microstructure was synthesized via calcination of a Zn–Co MOF precursor at an appropriate temperature. The as-prepared ZnCo2O4 sample presented good electrocatalytic oxygen evolution reaction performance with a small overpotential (η10 = 389 mV) and high stability in basic electrolyte. Furthermore, in basic medium, the as-synthesized ZnCo2O4 micro-rice also showed good electrocatalytic activity for glucose oxidation. A ZnCo2O4 micro-rice modified glass carbon electrode may be used as a potential non-enzymatic glucose sensor. The excellent electrocatalytic OER and glucose oxidation performances of ZnCo2O4 might be attributed to the unique porous structure formed by the nanoparticles. The porous architecture of the micro-rice can provide a large number of electrocatalytically active sites and high electrochemical surface area (ECSA). The result may offer a new way to prepare low-cost and high performance oxygen evolution reaction and glucose oxidation electrocatalysts.A porous ZnCo2O4 micro-rice like microstructure was synthesized via calcination of a Zn–Co MOF precursor at an appropriate temperature. 相似文献