Gene expression profile in rat small intestinal allografts after cold preservation/reperfusion

被引:5
|
作者
Wang, Shu-Feng [1 ]
Liang, Qi [2 ]
Li, Guo-Wei [3 ]
Gao, Kun [4 ]
机构
[1] Xi An Jiao Tong Univ, Dept Gen Surg, Hosp 1, Xian 710061, Shaanxi Provinc, Peoples R China
[2] Xian Tradit Chinese Hosp, Dept Anesthesiol, Xian 710001, Shaanxi Provinc, Peoples R China
[3] Xi An Jiao Tong Univ, Dept Gen Surg, Hosp 2, Xian 710004, Shaanxi Provinc, Peoples R China
[4] Xi An Jiao Tong Univ, Sch Life Sci, Xian 710049, Shaanxi Provinc, Peoples R China
基金
中国国家自然科学基金;
关键词
Small intestinal allografts; Cold preservation; Reperfusion Injury; Gene Expression Profiling;
D O I
10.3748/wjg.v11.i6.885
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To determine the changes of gene expression profile in small intestinal allografts in rats after cold preservation/reperfusion, and to identify the genes relevant to cold preservation/reperfusion injury. METHODS: Heterotopic segmental small bowel transplantation was performed in six rats with a sham operation and they were used as controls. Total RNA was extracted from the allografts (experimental group) and normal intestines (control group) 1 h after cold preservation/reperfusion, and then purified to mRNA, which was then reversely transcribed to cDNA, and labeled with fluorescent Cy5-dUTP and Cy3-dUTP to prepare hybridization probes. The mixed probes were hybridized to the cDNA microarray. After high-stringent washing, the fluorescent signals on cDNA microarray chip were scanned and analyzed. RESULTS: Among the 4 096 target genes, 82 differentially expressed genes were identified between the two groups. There were 18 novel genes, 33 expression sequence tags, and 31 previously reported genes. The selected genes may be divided into four classes: genes modulating cellular adhesion, genes regulating cellular energy, glucose and protein metabolism, early response genes and other genes. CONCLUSION: A total of 82 genes that may be relevant to cold preservation/reperfusion injury in small intestinal allografts are identified. Abnormal adhesion between polymorphonuclears and endothelia and failure in energy, glucose and protein metabolism of the grafts may contribute to preservation/reperfusion injury. The functions of the novel genes identified in our study need to be clarified further. (C) 2005 The WJG Press and Elsevier Inc. All rights reserved.
引用
收藏
页码:885 / 889
页数:5
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