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Endothelial cells in endogenous and transplanted pancreatic islets: differences in the expression of angiogenic peptides and receptors
Uppsala universitet, Institutionen för medicinsk cellbiologi.
Uppsala universitet, Institutionen för medicinsk cellbiologi.ORCID-id: 0000-0003-3047-6176
Uppsala universitet, Institutionen för medicinsk cellbiologi.
Uppsala universitet, Institutionen för medicinsk cellbiologi.
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2006 (Engelska)Ingår i: Pancreatology (Print), ISSN 1424-3903, E-ISSN 1424-3911, Vol. 6, nr 1-2, s. 86-95Artikel i tidskrift (Refereegranskat) Published
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Abstract [en]

Background/Aims: An important reason for the large amount of islets required for successful islet transplantation is likely to be inadequate engraftment of the transplanted islets. Thus, the revascularization is of major importance for graft survival. In order to study the expression of angiogenic peptides and receptors on islet endothelial cells (EC), we needed methods giving access to such endothelium. Therefore, we developed methods to isolate EC from islets transplanted intraportally or beneath the kidney capsule. Methods: Pancreatic islets were isolated, cultured and syngeneically transplanted into the liver or beneath the kidney capsule of C57BL/6 mice. One month post-transplantation, the islets were retrieved and EC from these islets were explanted. EC were also collected from freshly isolated and cultured non-transplanted islets. The EC were purified with Dynabeads and identified with immunocytochemistry. Angiogenesis GEArray technology was used to study angiogenic gene expression. Results: Several angiogenic genes were expressed in EC; e. g. endostatin, pigment-epithelial derived factor, vascular endothelial growth factor and angiopoietin-2, and their expression were affected by culture. Conclusion: The expression of angiogenesis-related genes in islet EC from non-transplanted islets is affected by culture. Moreover, we also describe a technique, which makes it possible to obtain EC from transplanted islets.

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2006. Vol. 6, nr 1-2, s. 86-95
Nyckelord [en]
Animals, Cells; Cultured, Endothelial Cells/metabolism/*physiology, Immunohistochemistry, Islets of Langerhans/*cytology/metabolism, Islets of Langerhans Transplantation/*physiology, Kidney/metabolism/pathology, Liver/metabolism/pathology, Male, Mice, Mice; Inbred C57BL, Neovascularization; Pathologic/*metabolism/pathology, Peptide Hormones/*physiology, Plant Lectins, RNA/biosynthesis
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Medicin och hälsovetenskap
Identifikatorer
URN: urn:nbn:se:miun:diva-27516DOI: 10.1159/000090027ISI: 000244256700012OAI: oai:DiVA.org:miun-27516DiVA, id: diva2:922941
Tillgänglig från: 2016-04-25 Skapad: 2016-04-25 Senast uppdaterad: 2018-04-20Bibliografiskt granskad

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Förlagets fulltexthttp://www.ncbi.nlm.nih.gov/pubmed/16327285?dopt=Citation

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