Expression of surface and intracellular specific markers by human stem cells derived from Lipostem™-treated adipose tissue

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Background: The antiproliferative effects of immunosuppressive drugs such as sirolimus and tacrolimus used in human islet transplantation interfere with the capacity of β cells to balance cell renewal and cell loss. This feature may be an important contributor to progressive graft dysfunction in islet transplant recipients over time. We analyzed the influence of different immunosuppressants on ɑ and β cell proliferation and transplant outcome following syngeneic β cell transplantation in mice.

Methods: Syngeneic islets (300 IP) were injected into the right liver lobes of C57BL/6 diabetic recipients. Osmotic pumps filled with bromodeoxyuridine (BrdU)(control) or BrdU and an immunosuppressant [tacrolimus, sirolimus, everolimus, or mycophenolate mofetil (MMF)] were implanted. Glycemic control was assessed using glucose tolerance tests. After four weeks, proliferation of ɑ and β cells was detected by BrdU incorporation. In addition, fractional β cell area and average β cell size was determined by morphometric analysis. Results: The average blood glucose levels were significantly higher in all treatment groups compared to controls. Glucose tolerance was improved only in control animals (P 0.009). The fractional β cell area and β cell proliferation in MMF-treated mice were comparable to control mice (P= 0.66). In contrast, treatment with everolimus and sirolimus led to a significant reduction in β cell proliferation and fractional β cell area. While transplanted β cells from animals treated with tacrolimus also presented a reduced replication rate (P= 0.023), the fractional β cell area was not affected compared to untreated controls (P= 0.72). Conclusions: Our …


A Raspa, S Carelli, F Messaggio, G Marfia, C Tremolada, AM Di Giulio, A Gorio


International Xenotransplantation Association