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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00002729naa a2200289 4500
001oai:prod.swepub.kib.ki.se:1943118
003SwePub
008240902s2005 | |||||||||||000 ||eng|
024a http://kipublications.ki.se/Default.aspx?queryparsed=id:19431182 URI
024a https://doi.org/10.2337/diabetes.54.8.22872 DOI
040 a (SwePub)ki
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Nyqvist, Du Karolinska Institutet4 aut
2451 0a Donor islet endothelial cells participate in formation of functional vessels within pancreatic islet grafts
264 1b American Diabetes Association,c 2005
520 a Pancreatic islet transplantation has emerged as a therapy for type 1 diabetes and is today performed using both freshly isolated and cultured islets. Islet blood vessels are disrupted during islet isolation; therefore, proper revascularization of the transplanted islets is of great importance for islet graft function and survival. We have studied intraislet endothelial cells after islet isolation, during islet culture, and following islet transplantation. By isolating islets from the transgenic Tie2-GFP (green fluorescent protein) mouse, characterized by an endothelial cell–specific expression of GFP, living endothelial cells could be studied in intact islets utilizing two-photon laser-scanning microscopy (TPLSM). Intraislet endothelial cells were found to survive islet transplantation but to rapidly disappear during islet culture. By transplanting freshly isolated Tie2-GFP islets and applying a novel ex vivo model for simultaneous perfusion and TPLSM imaging of the graft-bearing kidneys, GFP fluorescent endothelial cells were found to extensively contribute to vessels within the islet graft vasculature. Real-time imaging of the flow through the islet graft vasculature confirmed that the donor-derived vessels were functionally integrated. Hence, intraislet endothelial cells have the capability of participating in revascularization of pancreatic islets subsequent to transplantation. Therefore, preservation of intraislet endothelial cell mass may improve long-term graft function.
700a Kohler, Mu Karolinska Institutet4 aut
700a Wahlstedt, H4 aut
700a Berggren, POu Karolinska Institutet4 aut
710a Karolinska Institutet4 org
773t Diabetesd : American Diabetes Associationg 54:8, s. 2287-2293q 54:8<2287-2293x 0012-1797x 1939-327X
856u http://diabetes.diabetesjournals.org/content/54/8/2287.full.pdf
8564 8u http://kipublications.ki.se/Default.aspx?queryparsed=id:1943118
8564 8u https://doi.org/10.2337/diabetes.54.8.2287

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Nyqvist, D
Kohler, M
Wahlstedt, H
Berggren, PO
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Diabetes
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Karolinska Institutet

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