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An Isolated Venous Sac as a Novel Site for Cell Therapy in Diabetes Mellitus
Authors:Zurab Kakabadze  Koba Shanava  Camillo Ricordi  A M James Shapiro  Sanjeev Gupta  Ekaterine Berishvili
Institution:1 Department of Clinical Anatomy, Tbilisi State Medical University, and Division of Cell Transplantation, Georgian National Institute of Medical Research, DRI Federation, Tbilisi, GA. 2 Cell Transplant Center and Diabetes Research Institute, University of Miami, Diabetes Research Institute Federation, Miami, FL. 3 Clinical Islet Transplant Program and Department of Surgery, University of Alberta, Diabetes Research Institute Federation, Edmonton, Alberta, Canada T6G 1T7. 4 Departments of Medicine and Pathology, Diabetes Center, Marion Bessin Liver Research Center, Cancer Center, Gottesman Institute for Stem Cell Research and Regenerative Medicine, and Institute for Clinical and Translational Research, Albert Einstein College of Medicine, Bronx, NY. 5 Address correspondence to: Ekaterine Berishvili, M.D., Ph.D., Tbilisi State Medical University, 33 Vaja Pshavela Ave., 0177 Tbilisi, GA.
Abstract:BACKGROUND: Transplanting pancreatic islets is of significant interest for type 1 diabetes mellitus. After intraportal injection of islets, inferior engraftment and eventual loss of transplanted islets constitute major limitations. Therefore, alternative approaches will be helpful. Here, we evaluated in animals whether an isolated venous sac would support survival of transplanted islets, along with correction of hyperglycemia. METHODS: Pancreatic islets isolated from adult Lewis rats were transplanted either into an isolated venous sac made from lumbar vein or into the portal vein of syngeneic rats. The integrity and vascular organization of the venous sac was determined by studies of the local microcirculation. The engraftment, survival, and function of transplanted islets were analyzed by histology, including endocrine function in situ and by glycemic control in rats with streptozotocin-induced diabetes. RESULTS: Transplanted islets showed normal morphology with insulin expression in isolated venous sac during the long term. Transplanted islets received blood supply from vasa vasorum and had access to drainage through venous tributaries in the venous sac. This resulted in restoration of euglycemia in diabetic rats. Removal of islet graft-bearing venous sac in diabetic rats led to recurrence of hyperglycemia. By contrast, euglycemia was not restored in rats treated by intraportal transplantation of islets. CONCLUSIONS: We demonstrated that pancreatic islets successfully engrafted and functioned in the isolated venous sac with ability to restore euglycemia in diabetic rats. Therefore, the isolated venous sac offers a new site for transplantation of pancreatic islets. This would be clinically beneficial as an alternative to intrahepatic islet transplantation.
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