Details

Autor(en) / Beteiligte

• Potter, K. J.
• Werner, I.
• Denroche, H. C.
• Montane, J.
• Plesner, A.
• Chen, Y.
• Lei, D.
• Soukhatcheva, G.
• Warnock, G. L.
• Oberholzer, J.
• Fraser, P. E.
• Verchere, C. B.

Titel

Amyloid Formation in Human Islets Is Enhanced by Heparin and Inhibited by Heparinase

Ist Teil von

• American journal of transplantation, 2015-06, Vol.15 (6), p.1519-1530

Ort / Verlag

United States: Elsevier Limited

Erscheinungsjahr

2015

Quelle

Wiley-Blackwell Journals

Beschreibungen/Notizen

• Islet transplantation is a promising therapy for patients with diabetes, but its long‐term success is limited by many factors, including the formation of islet amyloid deposits. Heparin is employed in clinical islet transplantation to reduce clotting but also promotes fibrillization of amyloidogenic proteins. We hypothesized that heparin treatment of islets during pre‐transplant culture may enhance amyloid formation leading to beta cell loss and graft dysfunction. Heparin promoted the fibrillization of human islet amyloid polypeptide (IAPP) and enhanced its toxicity to INS‐1 beta cells. Heparin increased amyloid deposition in cultured human islets, but surprisingly decreased islet cell apoptosis. Treatment of human islets with heparin prior to transplantation increased the likelihood of graft failure. Removal of islet heparan sulfate glycosaminoglycans, which localize with islet amyloid deposits in type 2 diabetes, by heparinase treatment decreased amyloid deposition and protected against islet cell death. These findings raise the possibility that pretransplant treatment of human islets with heparin could potentiate IAPP aggregation and amyloid formation and may be detrimental to subsequent graft function. Treatment of human islets with heparin prior to transplantation enhances islet amyloid formation and impairs human islet graft function in a mouse model of diabetes.