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Reversal of hyperglycaemia 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 hyperglycaemia 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 to 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 5x10E5 BOEC resulted in reversal of hyperglycaemia, improved glucose tolerance and increased kidney insulin content.
The present study provides evidence that (i) previous packing in a blood clot
results in more effective islet delivery compared to tubing; (ii) 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
  • WoS Id: 000330384200003
  • ORCID: /0000-0001-7905-1289/work/104924630
  • ORCID: /0000-0001-5758-9547/work/76554345
  • ORCID: /0000-0003-1954-7375/work/61225815
  • ORCID: /0000-0002-0542-5708/work/60643895
  • Scopus Id: 84894421850
  • PubMed Id: 24213480
  • DOI: https://doi.org/10.4161/isl.26778
  • PubMed Central Id: PMC4010571
CSS-citation score:1
Toegankelijkheid:Closed