Primary culture of porcine pancreatic acinar cells

Introduction: The methodology of acinar cell culture has become of primary importance in the research of pancreatic physiology and pharmacology. Aim: To develop a method for primary culture of porcine pancreatic acinar cells. Methodology: Dispersed pancreatic acinar cells were made by RPMI-1640 medium containing collagenase III. After purification, the isolated acinar cells were cultured in RPMI-1640 medium with 2.5% fetal bovine serum. The morphologic characteristics of acinar cells were described. H-3-thymidine incorporation of acinar cells and activity of amylase or lipase were determined during the culture. Results: There were no remarkable morphologic changes in the pancreatic acinar cells during the 20-day Culture. The acini showed the tendency of gathering but did not attach to the walls of the Culture disks. Incorporation of H-3-thymidine in acinar cells in the primary culture was well kept. The secretion of amylase or lipase from acini decreased with the time of culture. Conclusions: In the primary culture of acinar cells from porcine pancreas developed in this study, the acinar cells retained normal morphology and ability of growth but not secretion of amylase or lipase. The method Would be beneficial for further experiments on acini of porcine pancreas.