Characterization of gene expression profile in rat Kupffer cells stimulated with IFN-alpha or IFN-gamma
- PMID: 16807150
- DOI: 10.1016/j.dld.2006.04.015
Characterization of gene expression profile in rat Kupffer cells stimulated with IFN-alpha or IFN-gamma
Abstract
Background and aim: Kupffer cells are intrasinusoidal space located macrophages with phagocytic capacity. Interferons are cytokines with antiviral, antiproliferative and immunomodulatory activities which may influence the activity of Kupffer cells. Aim of this study was to evaluate Kupffer cell gene expression after interferon-alpha or interferon-gamma stimulation in order to investigate a link between these cytokines and macrophage activation.
Methods: Rat Kupffer cells were cultured for 24 h and divided into three groups: unstimulated; stimulated with interferon-alpha and stimulated with interferon-gamma. After 8 h stimulation total RNA was extracted and processed according to Affymetrix protocols and hybridised on R34A microarray gene set. Data analyses was performed using Microarray Analysis Suite 5.0 software. Genes showing remarkably different expression in microarray analysis were confirmed by real-time PCR.
Results: Nearly 4000 out of the 8800 genes represented in the array were expressed by Kupffer cells. Among these, interferon-alpha up-regulates 91 genes by over two-fold (antiviral, antigen processing and presentation, and tumour suppressor/proapoptotic genes) and down-regulates 72 genes by 50% or more. Interferon-gamma up-regulates 70 genes by over two-fold and down-regulates 78 genes by 50% or more. Most of the genes induced by interferon-alpha are also induced by interferon-gamma. Down-regulated genes include growth factors and genes involved in cell cycle/proliferation. Real-time PCR confirms the results of the array.
Conclusion: Interferons directly target rat Kupffer cells and are involved in the regulation of a wide variety of genes. Their expression profile shed light onto molecular mechanism of Kupffer cells activation in specific pathways such as antiviral and antitumour processes.
Similar articles
-
Analysis of gene expression in hepatitis B virus transfected cell line induced by interferon.Sheng Wu Hua Xue Yu Sheng Wu Wu Li Xue Bao (Shanghai). 2003 Dec;35(12):1053-60. Sheng Wu Hua Xue Yu Sheng Wu Wu Li Xue Bao (Shanghai). 2003. PMID: 14673494
-
Unique keratinocyte-specific effects of interferon-gamma that protect skin from viruses, identified using transcriptional profiling.Antivir Ther. 2003 Dec;8(6):541-54. Antivir Ther. 2003. PMID: 14760888
-
Oligonucleotide microarray analysis of human lens epithelial cells: TGFbeta regulated gene expression.Mol Vis. 2007 Jul 17;13:1181-97. Mol Vis. 2007. PMID: 17679943
-
Biological activity of gamma interferon.Ann Ist Super Sanita. 1990;26(3-4):255-61. Ann Ist Super Sanita. 1990. PMID: 2128676 Review.
-
Interferon-gamma: an overview of signals, mechanisms and functions.J Leukoc Biol. 2004 Feb;75(2):163-89. doi: 10.1189/jlb.0603252. Epub 2003 Oct 2. J Leukoc Biol. 2004. PMID: 14525967 Review.
Cited by
-
Functional heterogeneity of CD4+ T cells in liver inflammation.Semin Immunopathol. 2021 Aug;43(4):549-561. doi: 10.1007/s00281-021-00881-w. Epub 2021 Aug 31. Semin Immunopathol. 2021. PMID: 34463867 Free PMC article. Review.
-
Elevated interferon gamma signaling contributes to impaired regeneration in the aged liver.J Gerontol A Biol Sci Med Sci. 2011 Sep;66(9):944-56. doi: 10.1093/gerona/glr094. Epub 2011 Jun 30. J Gerontol A Biol Sci Med Sci. 2011. PMID: 21719609 Free PMC article.
-
Myeloid STAT3 inhibits T cell-mediated hepatitis by regulating T helper 1 cytokine and interleukin-17 production.Gastroenterology. 2009 Dec;137(6):2125-35.e1-2. doi: 10.1053/j.gastro.2009.08.004. Epub 2009 Aug 15. Gastroenterology. 2009. PMID: 19686746 Free PMC article.
-
Proximal genomic localization of STAT1 binding and regulated transcriptional activity.BMC Genomics. 2006 Oct 11;7:254. doi: 10.1186/1471-2164-7-254. BMC Genomics. 2006. PMID: 17032459 Free PMC article.
-
IFN-α mediates the development of autoimmunity both by direct tissue toxicity and through immune cell recruitment mechanisms.J Immunol. 2011 Apr 15;186(8):4693-706. doi: 10.4049/jimmunol.1002631. Epub 2011 Mar 14. J Immunol. 2011. PMID: 21402899 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources