1. [The influence with block the endotoxin signal transduction for ischemia/reperfusion injury of graft liver in rats]
- Author
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Zuo-jin, Liu, Sheng-wei, Li, Xu-hong, Li, Yong, Peng, Hai-bo, You, Shou-bai, Li, and Jian-ping, Gong
- Subjects
Graft Rejection ,Male ,Rats, Sprague-Dawley ,Interleukin-1 Receptor-Associated Kinases ,Liver ,Reperfusion Injury ,Animals ,RNA Interference ,Genetic Therapy ,Transfection ,Liver Transplantation ,Rats ,Signal Transduction - Abstract
To explore the feasibility of interleukin 1 receptor associated kinase-4 (IRAK-4) as gene therapy target for liver ischemia/reperfusion injury (I/RI) and effective approach in vivo for short hairpin RNA (shRNA) interference used to gene therapy in liver graft hqappened.Sprague-Dawley rats were randomly divided into three groups: the control group, the in vivo transfection group (IVT) and the cold ischemia transfection group (CIT). Experiments of orthotopic liver transplantation were performed by two-cuff method. CIT were perfused with IRAK-4-shRNA plasmid (pSIIRAK-4) during cold ischemia phase, IVT received the equivalent volumes (2 mL) of pSIIRAK-4 after portal vein inosculated, and the control group leaved without any treatment. At 0 min, 60 min and 180 min after reperfusion, the expression of IRAK-4 gene and protein level were determined by RT-PCR and Western blot. The serum TNF-alpha level was detected by ELISA. Liver histopathological changes and cell apoptosis were observed by electron microscope and TUNEL.After reperfusion, the expression of IRAK-4 were largely depressed in CIT than that of IVT and the control group (P0.01), and furthermore, the serum TNF-alpha level, proportion of hepatocyte apoptosis and severity of hepatocyte injury were also lower than the latter.These results indicate that depression IRAK-4 expression with IRAK-4-shRNA through portal vein perfusion during cold ischemia phase could effectively blunt graft hepatic I/RI.
- Published
- 2006