Wide gene expression profiling of ischemia-reperfusion injury in human liver transplantation

被引:47
作者
Conti, Anna
Scala, Simona
D'Agostino, Paola
Alimenti, Elena
Morelli, Danielle
Andria, Barbara
Tammaro, Angela
Attanasio, Chiara
Della Ragione, Floriana
Scuderi, Vincenzo
Fabbrini, Floriana
D'Esposito, Maurizio
Di Florio, Ernesto
Nitsch, Lucio
Calise, Fulvio
Faiella, Antonio
机构
[1] Antonio Cardarelli Hosp, Ctr Biotechnol, I-80131 Naples, Italy
[2] Univ Naples Federico II, Dept Biol & Cellular Pathol, Naples, Italy
[3] CNR, Inst Genet & Biophys A Buzzati Traverso, Naples, Italy
[4] Antonio Cardarelli Hosp, Liver Transplantat Unit, I-80131 Naples, Italy
关键词
D O I
10.1002/lt.20960
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Ischemia-reperfusion injury (IRI) causes up to 10% of early liver failures in humans and can lead to a higher incidence of acute and chronic rejection. So far, very few studies have investigated wide gene expression profiles associated with the IRI process. The discovery of novel genes activated by IRI might lead to the identification of potential target genes for the prevention or treatment of the injury. In our study, we compared gene expression levels in reperfused livers (RL group) vs. the basal values before retrieval from the donor (basal liver [BL] group) using oligonucleotide array technology. We examined 10 biopsies from 5 livers, analyzing approximately 33,000 genes represented on the Affymetrix HG-U133APlus 2.0 oligonucleotide arrays (Affymetrix, Santa Clara, CA). About 13,000 individual genes were considered expressed in at least 1 condition. A total of 795 genes whose expression is significantly modified by ischemia-reperfusion in human liver transplantation were identified in this study. Some of them are likely to be completely activated by IRI, as they are not expressed in basal livers. The supervised gene expression analysis revealed that at least 12% of the genes involved in the apoptotic process, 12.5% of the genes involved in inflammatory processes, and 22.5% of the genes encoding for heat shock proteins are differentially expressed in RL samples vs. BL samples. Furthermore, IRI induces the upregulation of some genes' coding for adhesion molecules and integrins. In conclusion, we have identified a relevant amount of early genes regulated in the human liver after 7-9 hours of cold ischemia and 2 hours from reperfusion, many of them not having been described before in this process. Their analyses may help us to better understand the pathophysiology of IRI and to characterize potential target genes for the prevention or treatment of the liver injury in order to increase the number of patients that successfully undergo transplantation.
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页码:99 / 113
页数:15
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