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Reversal of hyperglycemia in diabetic mice by a marginal islet mass together with human blood outgrowth endothelial cells is independent of the delivery technique and blood clot-induced processes

Tijdschriftbijdrage - Tijdschriftartikel

We recently reported that human blood outgrowth endothelial cells (BOEC) are supportive to reverse hyperglycemia in marginal islet mass-transplanted diabetic mice. In this report, we investigated whether the observed effect was evoked by islet packing in a blood clot prior to transplantation or could be mimicked by another method of islet/cell delivery. A marginal islet mass with or without BOEC was grafted underneath the kidney capsule of diabetic recipient mice via a (blood clot-independent) tubing system and compared with previous islet packing in a blood clot. The effect on metabolic outcome of both delivery techniques as well as the additive effect of BOEC was subsequently evaluated. Marginal islet mass transplantation via a tubing system required more islets per recipient than via a blood clot. Using the tubing method, transplantation of a marginal islet mass combined with 5x10 (5) BOEC resulted in reversal of hyperglycemia, improved glucose tolerance and increased kidney insulin content. The present study provides evidence that (1) previous packing in a blood clot results in more effective islet delivery compared with tubing; (2) BOEC exert a beneficial effect on marginal islet transplantation, independent of grafting technique and potential blood clot-induced processes. These data further support the use of BOEC in (pre-) clinical studies that aim to improve current islet transplantation protocols.

Tijdschrift: Islets
ISSN: 1938-2014
Issue: 5
Volume: 5
Pagina's: 196-200
Jaar van publicatie:2013
Trefwoorden:Animals, Blood Coagulation, Blood Glucose/metabolism, Diabetes Mellitus, Experimental/surgery, Endothelial Cells/transplantation, Humans, Hyperglycemia/surgery, Islets of Langerhans/physiology, Islets of Langerhans Transplantation/methods, Male, Mice, Mice, Inbred NOD, Mice, SCID