Adenoviral bcl-2 transfer improves survival and early graft function after ischemia and reperfusion in rat liver transplantation

Rentsch, M. and Kienle, Klaus and Mueller, Thomas and Vogel, Mandy and Jauch, K. W. and Puellmann, Kerstin and Obed, Aiman and Schlitt, Hans Juergen and Beham, Alexander (2005) Adenoviral bcl-2 transfer improves survival and early graft function after ischemia and reperfusion in rat liver transplantation. TRANSPLANTATION, 80 (10). pp. 1461-1467. ISSN 0041-1337, 1534-6080

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Abstract

Background. Primary graft dysfunction due to ischemia and reperfusion injury represents a major problem in liver transplantation. The related cell stress may induce apoptosis, which can be suppressed by bcl-2. The purpose of the study was to investigate the effect of adenoviral bcl-2 gene transfer on early graft function and survival in rat liver transplantation. Methods. An adenoviral construct that transfers bcl-2 under the control of a tetracycline inducible promoter was generated (advTetOn bcl-2) and used with a second adenovirus that transfers the repressor protein (advCMV Rep). Forty-eight hours before explantation, donor rats were treated with advTetOn bcl-2/ advCMV Rep (n=7) and doxycyclin, with the control adenoviral construct advCMV GFP (n=8) or with doxycyclin alone (n=8). Liver transplantation was performed following 16 hours of cold storage (UW). Bcl-2 expression and intrahepatic apoptosis was assessed. Bile flow was monitored 90 min posttransplantation. The endpoint for survival was 7 days. Results. Bcl-2 was expressed in hcpatocytes and sinusoidal lining cells. This was associated with a significant reduction of apoptotic sinusoidal lining cells and hepatocytes after 24 hours and 7 days. Bile production was significantly higher following bcl-2 pretreatment. Furthermore, bcl-2 transfer resulted in significantly improved survival (100% vs. 50% both control groups). Conclusions. Adenoviral bcl-2 transfer results in protein expression in hepatocytes and sinusoidal lining cells resulting in early graft function and survival enhancement after prolonged ischemia and reperfusion injury. The inhibition of apoptosis in the context of liver transplantation might be a reasonable approach in the treatment of graft dysfunction.

Item Type: Article
Uncontrolled Keywords: SINUSOIDAL ENDOTHELIAL-CELLS; PRESERVATION INJURY; COLD ISCHEMIA; ANTIOXIDANT PATHWAY; GENE-TRANSFER; EARLY PHASE; APOPTOSIS; EXPRESSION; ACTIVATION; DEATH; bcl-2; liver transplantation; rat; adenovirus; graft survival; apoptosis
Subjects: 600 Technology > 610 Medical sciences Medicine
Divisions: Medicine > Lehrstuhl für Chirurgie
Depositing User: Dr. Gernot Deinzer
Date Deposited: 23 Apr 2021 06:10
Last Modified: 23 Apr 2021 06:10
URI: https://pred.uni-regensburg.de/id/eprint/35408

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