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Endocr J ; 51(3): 381-6, 2004 Jun.
Article in English | MEDLINE | ID: mdl-15256786

ABSTRACT

The present study was conducted in an attempt to treat streptozotocin (STZ)-induced hyperglycemia by transplanting beta cells derived from pancreatic ductal cells. Ductal cells obtained from neonatal rats were cultured in vitro. Approximately 70% of the cells were converted to insulin-secreting cells by incubating with betacellulin and activin A. Differentiated cells responded to a depolarizing concentration of potassium, tolbutamide and a high concentration of glucose, and insulin secretion increased by 2.5-, 2.3- and 1.6-fold, respectively. We then prepared pseudoislets using the differentiated cells, which exhibited greatly improved glucose-responsiveness, with a high concentration of glucose inducing a 3-fold increase in insulin secretion. We transplanted these pseudoislets into the portal vein of STZ-treated nude mice. Before transplantation, the plasma glucose concentration was above 400 mg/dl, and after transplantation it was markedly reduced, the effect of which persisted for two weeks. These results indicate that STZ-induced hyperglycemia can be treated by transplanting pseudoislets consisting of beta cells derived from ductal cells.


Subject(s)
Hyperglycemia/surgery , Islets of Langerhans Transplantation , Pancreatic Ducts/cytology , Pancreatic Ducts/transplantation , Animals , Blood Glucose/analysis , Cell Differentiation/drug effects , Cells, Cultured , Hyperglycemia/chemically induced , Insulin/metabolism , Insulin Secretion , Male , Mice , Mice, Nude , Portal Vein , Rats , Rats, Wistar , Streptozocin
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