Home LiteratureArticle Details
PMID: 12663442 Published · ppublish English Comparative Study Journal Article Research Support, U.S. Gov't, P.H.S.

Early changes in gene expression profiles of hepatic GVHD uncovered by oligonucleotide microarrays.

Blood ·Vol. 102 ·No. 2 ·2003-07-15 ·Pages 763-71

Ichiba T, Teshima T, Kuick R, Misek DE, Liu C, Takada Y, Maeda Y, Reddy P, Williams DL, Hanash SM, Ferrara JL

Abstract

The liver, skin, and gastrointestinal tract are major target organs of acute graft-versus-host disease (GVHD), the major complication of allogeneic bone marrow transplantation (BMT). In order to gain a better understanding of acute GVHD in the liver, we compared the gene expression profiles of livers after experimental allogeneic and syngeneic BMT using oligonucleotide microarray. At 35 days after allogeneic BMT when hepatic GVHD was histologically evident, genes related to cellular effectors and acute-phase proteins were up-regulated, whereas genes largely related to metabolism and endocrine function were down-regulated. At day 7 after BMT before the development of histologic changes in the liver, interferon gamma (IFN-gamma)-inducible genes, major histocompatibility (MHC) class II molecules, and genes related to leukocyte trafficking had been up-regulated. Immunohistochemistry demonstrated that expression of IFN-gamma protein itself was increased in the spleen but not in hepatic tissue. These results suggest that the increased expression of genes associated with the attraction and activation of donor T cells induced by IFN-gamma early after BMT is important in the initiation of hepatic GVHD in this model and provide new potential molecular targets for early detection and intervention of acute GVHD.

MeSH Terms
Acute-Phase Proteins/biosynthesis,genetics Animals Antigen Presentation/genetics Apoptosis/genetics Bone Marrow Transplantation/adverse effects Chemotaxis, Leukocyte/genetics Expressed Sequence Tags Female Gene Expression Profiling Gene Expression Regulation/drug effects Graft vs Host Disease/genetics,metabolism,pathology Inflammation/genetics Intercellular Adhesion Molecule-1/biosynthesis,genetics Interferon-gamma/biosynthesis,genetics,pharmacology Liver/drug effects,metabolism,pathology Lymphocyte Activation/genetics Mice Mice, Inbred C57BL Oligonucleotide Array Sequence Analysis Organ Specificity Radiation Chimera Spleen/metabolism T-Lymphocytes/immunology,metabolism Transplantation, Homologous/adverse effects Transplantation, Isogeneic
Chemicals
Acute-Phase Proteins Intercellular Adhesion Molecule-1 Interferon-gamma
Authors & Affiliations
11 authors, click to expand affiliations / ORCID
Ichiba Tamotsu
Department of Internal Medicine, University of Michigan Cancer Center, Ann Arbor, USA.
Teshima Takanori
Kuick Rork
Misek David E
Liu Chen
Takada Yuichiro
Maeda Yoshinobu
Reddy Pavan
Williams Debra L
Hanash Samir M
Ferrara James L M
Article Info
Journal
Blood
Abbr.
Blood
ISSN
0006-4971
Published
2003-07-15
Epub
2003-00-27
Pages
763-71
Language
English
Region
United States
NLM ID
7603509
Subset
IM
Grants
NCI NIH HHS · CA4592 · United States
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