Intragraft gene expression profiles by cDNA microarray in small-for-size liver grafts

Liver Transpl. 2003 Apr;9(4):425-32. doi: 10.1053/jlts.2003.50066.

Abstract

The aim of this study is to identify the molecular mechanism of small-for-size graft injury through large-scale expression measurement of intragraft gene profile by carrier DNA (cDNA) microarray screening in liver transplantation. The studies compared 1,081 intragraft genes expression profiles using cDNA microarray of small-for-size grafts (<30% of recipient liver weight) with those of whole grafts (control group) 1, 3, and 24 hours after reperfusion in a rat liver transplantation model. Intragraft gene expression was detected by quantitative reverse-transcriptase polymerase chain reaction (RT-PCR). Hepatic ultrastructural features were shown by electron microscopy. In the small-for-size grafts, by cDNA microarray study, the vasoconstriction genes were found up-regulated together with adhesion molecules at 1 hour after reperfusion. Three and 24 hours after reperfusion, the vasopressin genes were found up-regulated together with adhesion molecules, inflammatory mediators and cell death signals, accompanied with down-regulation of the genes related to energy metabolism. By quantitative RT-PCR, intragraft messenger RNA (mRNA) expression of endothelin-1 (ET-1) and endothelin-1 receptor A (ETA) was up-regulated during the first 24 hours after reperfusion accompanied with down-regulation of heme oxygenase-1 (HO-1). The intragraft mRNA and plasma levels of inflammatory cytokines (interleukin [IL]-6, IL-15, tumor necrosis factor [TNF]-alpha) also were overexpressed during the first 24 hours after reperfusion. Sinusoidal congestion and disruption were found accompanied with mitochondrial swelling during the first 24 hours after reperfusion. The up-regulation of intragraft vasoconstriction genes accompanied by early overexpression of adhesion molecules and apoptotic signals, as well as down-regulation of HO-1 in small-for-size grafts may be related to sinusoidal injury leading to graft damage in liver transplantation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Computer Systems
  • Cytokines / blood
  • Cytokines / genetics
  • Down-Regulation
  • Endothelin-1 / blood
  • Endothelin-1 / genetics
  • Enzyme-Linked Immunosorbent Assay
  • Gene Expression Profiling*
  • Heme Oxygenase (Decyclizing) / genetics
  • Heme Oxygenase-1
  • Liver / metabolism*
  • Liver / ultrastructure
  • Liver Transplantation / methods*
  • Male
  • Microscopy, Electron
  • Oligonucleotide Array Sequence Analysis*
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Endothelin / genetics
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • Cytokines
  • Endothelin-1
  • Receptors, Endothelin
  • Heme Oxygenase (Decyclizing)
  • Heme Oxygenase-1