2011 - IPITA - Prague


This page contains exclusive content for the member of the following sections: TTS, IPITA. Log in to view.

Parallel session 3 – Open oral presentations Topic: Stem cells

3.4 - Bone marrow stem cells and islet co-transplantation promotes graft revascularization and function in small intestinal submucosa

Presenter: E., Berishvili, Tbilisi, Georgia
Authors: E. Berishvili, Z. Kakabadze, I. Amiranashvili, K. Chutkerashvili


Bone marrow stem cells and islet co-transplantation promotes graft revascularization and function in small intestinal submucosa

E. Berishvili, Z. Kakabadze, I. Amiranashvili, K. Chutkerashvili
Tbilisi State Medical University, Tbilisi, Georgia

Objective: Type 1 diabetes is associated with aprogressive loss of beta cells and islet cell transplantation represents one ofthe most promising therapies. Recently we have shown that small intestinalsubmucosa is a sutable place for pancreatic islet transplantation. In thisstudy we show that transplantation of bone marrow cells into the smallintestinal submucosa allows minimal islet mass improve glycemic control in mousemodel.

Methods: Segments of small intestine were prepared by denudationof the mucosal layer prior to implantation. Streptozotocin induced diabetic C57Bl/6mice were transplanted syngeneically into the small intestinal submucosa withthe following: 100 islets alone (islet group: n = 12), 100 islets and 5 × 106bone marrow cells (islet-bone marrow group: n = 12) and sham operated group nocells (sham group: n = 5). Blood glucose levels were monitored andintraperitoneal glucose tolerance tests carried out. Histological assessment forinsulin, glucagon, von Willebrand factor (vWF) was performed.

Results: Co-transplantation of 100 islets and 5 × 106bone marrow cells reversed diabetes in all recipients, whereas islet-alonetransplantation achieved euglycemia in 2 of 12 recipients. Transplanted isletsdemonstrated expression of insulin and glucagon throughout the 90-day durationof the studies. Results of intravenous glucose tolerance tests performed on day56 were significantly better in islet-bone marrow group than islet-alonerecipients. One week after transplantation, well-preserved islet structure andhigher number of capillaries were found in the small intestinal segments ofislet- bone marrow recipients, whereas islet-alone grafts were fragmented withvery few capillaries. Removal of graft-bearing intestinal segments led torecurrence of hyperglycemia.

Conclusions: Islet co-transplantation with bone marrow isassociated with improvement of islet graft function.


Important Disclaimer

By viewing the material on this site you understand and accept that:

  1. The opinions and statements expressed on this site reflect the views of the author or authors and do not necessarily reflect those of The Transplantation Society and/or its Sections.
  2. The hosting of material on The Transplantation Society site does not signify endorsement of this material by The Transplantation Society and/or its Sections.
  3. The material is solely for educational purposes for qualified health care professionals.
  4. The Transplantation Society and/or its Sections are not liable for any decision made or action taken based on the information contained in the material on this site.
  5. The information cannot be used as a substitute for professional care.
  6. The information does not represent a standard of care.
  7. No physician-patient relationship is being established.

Social

Contact

Staff Directory
+1-514-874-1717
info@tts.org

Address

The Transplantation Society
International Headquarters
740 Notre-Dame Ouest
Suite 1245
Montréal, QC, H3C 3X6
Canada