Ducto-insular proliferation of beta-cells after syngeneic islet transplantation into the spleen of streptozotocin-diabetic lewis rats

1989 ◽  
Vol 5 (1) ◽  
pp. 77-83
Author(s):  
Frank Wohlrab ◽  
Siegfried Schmidt ◽  
Ingrid Klöting ◽  
Barbara Wilke ◽  
Lothar Cossel
Diabetes ◽  
1996 ◽  
Vol 45 (11) ◽  
pp. 1541-1546 ◽  
Author(s):  
V. Nacher ◽  
M. Raurell ◽  
J. F. Merino ◽  
O. Aranda ◽  
J. Soler ◽  
...  

Diabetes ◽  
1996 ◽  
Vol 45 (11) ◽  
pp. 1541-1546 ◽  
Author(s):  
V. Nacher ◽  
M. Raurell ◽  
J. F. Merino ◽  
O. Aranda ◽  
J. Soler ◽  
...  

2000 ◽  
Vol 9 (1) ◽  
pp. 11-18 ◽  
Author(s):  
Juan F. Merino ◽  
Victor Nacher ◽  
Mercè Raurell ◽  
Montserrat Biarnés ◽  
Joan Soler ◽  
...  

2007 ◽  
Vol 192 (1) ◽  
pp. 169-177 ◽  
Author(s):  
Marta Montolio ◽  
Montse Biarnés ◽  
Noèlia Téllez ◽  
Jessica Escoriza ◽  
Joan Soler ◽  
...  

Islets are particularly vulnerable in the initial days after transplantation when cell death results in the loss of more than half of the transplanted islet tissue. To determine whether a non-specific inflammation at the grafted site mediated by the local expression of inflammatory cytokines could play a role on the initial damage to transplanted islets, we studied the expressions of interleukin-1β (IL-1β) and inducible form of nitric oxide synthase (iNOS) after syngeneic islet transplantation. Insulin-treated streptozotocin-diabetic Lewis rats were syngeneically transplanted with 500 islets. Grafts were harvested 1, 3, or 7 days after transplantation, and the expressions of IL-1β and iNOS genes were determined by RT-PCR. IL-1β and iNOS mRNAs were detected in islets immediately after isolation, and were upregulated after transplantation. IL-1β mRNA was ninefold increased on day 1, was still sevenfold increased on day 3 after transplantation, and declined towards pretransplantation levels on day 7. iNOS mRNA showed a similar pattern of expression to that of IL-1β: on days 1 and 3 after transplantation it was 14-and 4-fold higher respectively than in freshly isolated islets. In addition, IL-1β and iNOS were identified in islet grafts and found to be produced mainly by CD68-positive macrophages. A low number of IL-1β- and iNOS-positive but CD68-negative cells were also identified suggesting that other cell types, in addition to macrophages, were involved in the expression of IL-1β and NO production in islet grafts. The finding of increased IL-1β and iNOS gene expressions in the initial days after islet transplantation and the presence of IL-β and iNOS proteins in the graft confirmed the presence of an early non-specific inflammatory response after islet transplantation. Overall, the data suggest that IL-1β plays a role in the extensive β-cell death found in the initial days after islet transplantation.


2005 ◽  
Vol 14 (8) ◽  
pp. 595-605 ◽  
Author(s):  
Craig R. Halberstadt ◽  
Deana Williams ◽  
Dwaine Emerich ◽  
Moses Goddard ◽  
Alfred V. Vasconcellos ◽  
...  

Pancreatic islet transplantation into type 1 diabetic patients is currently being performed by intraportal infusion. This method, albeit reproducible, has some disadvantages including potential development of portal hypertension, hemorrhage, and an inability to retrieve or detect the transplanted tissue. Other transplant sites have been examined in animal models including the omentum, peritoneal cavity, and the spleen. A transplant site that has not been successful in supporting functional islet tissue transplantation in humans is the subcutaneous space due primarily to the lack of a well-defined vascular bed. This site has many favorable characteristics such as ease of access for transplantation and potential for removal of the transplanted tissue with a minimally invasive surgical procedure. This report addresses the evaluation of a subcutaneously placed device for the support of rat syngeneic islet transplantation in a streptozocin-induced diabetic model. The data generated support the use of this device for islet engraftment. In addition, beta cell function in this device compared favorably with the function of islets transplanted to the renal subcapsular space as well as islets within the native pancreas.


Autoimmunity ◽  
1993 ◽  
Vol 15 (2) ◽  
pp. 107-112 ◽  
Author(s):  
B. Kuttler ◽  
C. Mathieu ◽  
M. Waer ◽  
H. J. Hahn ◽  
R. Bouillon

2015 ◽  
Vol 99 (11) ◽  
pp. 2294-2300 ◽  
Author(s):  
Andrew R. Pepper ◽  
Rena Pawlick ◽  
Boris Gala-Lopez ◽  
Amanda MacGillivary ◽  
Delfina M. Mazzuca ◽  
...  

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