Intraislet endothelial cells contribute to revascularization of transplanted pancreatic islets.

Brissova M, Fowler M, Wiebe P, Shostak A, Shiota M, Radhika A, Lin PC, Gannon M, Powers AC
Diabetes. 2004 53 (5): 1318-25

PMID: 15111502 · DOI:10.2337/diabetes.53.5.1318

Pancreatic islet transplantation is an emerging therapy for type 1 diabetes. To survive and function, transplanted islets must revascularize because islet isolation severs arterial and venous connections; the current paradigm is that islet revascularization originates from the transplant recipient. Because isolated islets retain intraislet endothelial cells, we determined whether these endothelial cells contribute to the revascularization using a murine model with tagged endothelial cells (lacZ knock-in to Flk-1/VEGFR2 gene) and using transplanted human islets. At 3-5 weeks after transplantation beneath the renal capsule, we found that islets were revascularized and that the transplant recipient vasculature indeed contributed to the revascularization process. Using the lacZ-tagged endothelial cell model, we found that intraislet endothelial cells not only survived after transplantation but became a functional part of revascularized islet graft. A similar contribution of intraislet endothelial cells was also seen with human islets transplanted into an immunodeficient mouse model. In the murine model, individual blood vessels within the islet graft consisted of donor or recipient endothelial cells or were a chimera of donor and recipient endothelial cells, indicating that both sources of endothelial cells contribute to the new vasculature. These observations suggest that interventions to activate, amplify, or sustain intraislet endothelial cells before and after transplantation may facilitate islet revascularization, enhance islet survival, and improve islet transplantation.

MeSH Terms (18)

Animals Animals, Genetically Modified Biomarkers Cell Survival Endothelium, Vascular Humans In Vitro Techniques Islets of Langerhans Kidney Mice Mice, Inbred C57BL Mice, Inbred NOD Mice, SCID Neovascularization, Physiologic Pancreas Transplantation, Heterologous Transplantation, Heterotopic Vascular Endothelial Growth Factor Receptor-2

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