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1.
Journal of Huazhong University of Science and Technology (Medical Sciences) ; (6): 529-533, 2016.
Article in English | WPRIM | ID: wpr-285234

ABSTRACT

Intraportal transplantation of islets is no longer considered to be an ideal procedure and finding the extrahepatic alternative site is becoming a subject of high priority. Herein, in this study, we would introduce our initial outcomes of using gastric submucosa (GS) and liver as sites of islet autotransplantation in pancreatectomized diabetic Beagles. Total pancreatectomy was performed in Beagles and then their own islets extracted from the excised pancreas were transplanted into GS (GS group, n=8) or intrahepatic via portal vein (PV group, n=5). Forty-eight hours post transplantation, graft containing tissue harvested from the recipients revealed the presence of insulin-positive cells. All recipients in GS group achieved euglycemia within 1 day, but returned to a diabetic state at 6 to 8 days post-transplantation (mean survival time, 7.16±0.69 days). However, all of the animals kept normoglycemic until 85 to 155 days post-transplantation in PV group (mean survival time, 120±28.58 days; P<0.01 vs. GS group). The results of intravenous glucose tolerance test (IVGTT) confirmed that the marked improvement in glycometabolism was obtained in intrahepatic islet autotransplantation. Thus, our findings indicate that the liver is still superior to the GS as the site of islet transplantation, at least in our islet autotransplant model in pancreatectomized diabetic Beagles.


Subject(s)
Animals , Dogs , Humans , Diabetes Mellitus, Experimental , Metabolism , Pathology , Therapeutics , Gastric Mucosa , Metabolism , Transplantation , Glucose , Metabolism , Glucose Tolerance Test , Graft Survival , Insulin , Metabolism , Islets of Langerhans Transplantation , Liver , Pathology , Liver Transplantation , Transplantation, Autologous
2.
Chinese Journal of Surgery ; (12): 331-334, 2007.
Article in Chinese | WPRIM | ID: wpr-342171

ABSTRACT

<p><b>OBJECTIVE</b>To modify the isolation and culture method of Sertoli cells and investigate its' effects on xeno-lymphocytes apoptosis.</p><p><b>METHODS</b>Sertoli cells which was isolated from 2 - 4 week-old Sprague Dawley (SD) rats, were successfully prepared by collagenase type V, trypsin and DNase I and then identified by electron microscope. Viability and apoptosis of cultured cells were measured by flow cytometry. The apoptosis rates of Balb/c mouse lymphocytes were examined which were co-cultured with Sertoli cells of SD rats by flow cytometry, too. The expression of FasL, TGF-beta(1) and clusterin on Sertoli cells were detected by immunocytochemistry.</p><p><b>RESULTS</b>In the co-cultured system, Sertoli cells accounted for more than 90%. The viability of Sertoli cells was above 95% and the apoptosis rate was 10.87% +/- 3.87% in this study. The lymphocytes apoptosis ratio was 15.52% +/- 0.17% (P < 0.01). Streptavidin-biotin-peroxidase-complex immunochemistry staining showed that the Sertoli cells could express FasL, TGF-beta(1) and clusterin, respectively.</p><p><b>CONCLUSIONS</b>It indicates that the expression of FasL, TGF-beta(1) on the Sertoli cells might relate to the immune privilege, and it supposed to be benefit for xenotransplantation.</p>


Subject(s)
Animals , Male , Mice , Rats , Apoptosis , Cell Culture Techniques , Methods , Cell Survival , Physiology , Cells, Cultured , Clusterin , Metabolism , Coculture Techniques , Fas Ligand Protein , Metabolism , Flow Cytometry , Immunohistochemistry , Lymphocytes , Cell Biology , Physiology , Mice, Inbred BALB C , Microscopy, Electron, Transmission , Rats, Sprague-Dawley , Sertoli Cells , Cell Biology , Metabolism , Transforming Growth Factor beta , Metabolism
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