Abstract
The liver is an important site of host-microbe interaction. Although hepatocytes have been reported to be responsive to lipopolysaccharide (LPS), the global gene expression changes by LPS and mechanism(s) by which LPS stimulates cultured hepatocytes remain uncertain. Cultures of primary mouse hepatocytes were incubated with LPS to assess its effects on the global gene expression, hepatic transcription factors, and mitogen-activated protein (MAP) kinase activation. DNA microarray analysis indicated that LPS modulates the selective expression of more than 80 genes and expressed sequence tags. We have shown previously that hepatocytes express CD14, which is required both for uptake and responsiveness to LPS. In other cells, responsiveness to microbial products requires expression of Toll-like receptors (TLR) and their associated accessory molecules. Hepatocytes expressed TLR1 through TLR9 as well as MyD88 and MD-2 transcripts, as shown by reverse transcriptase PCR analysis, indicating that hepatocytes express all known microbe recognition molecules. The MAP kinase extracellular signal-regulated kinase 1/2 was phosphorylated in response to LPS in mouse hepatocytes, and the levels of phosphorylation were lower in hepatocytes from TLR4-null mice. NF-kappa B activation was reduced in TLR4-mutant or -null hepatocytes compared to control hepatocytes, and this defect was partially restored by adenoviral transduction of mouse TLR4. Thus, hepatocytes respond to nanogram concentrations of LPS through a TLR4 response pathway.
Publication types
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Adaptor Proteins, Signal Transducing
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Adenoviridae
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Animals
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Antigens, Differentiation / genetics
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Antigens, Surface / genetics
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Cells, Cultured
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Drosophila Proteins*
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Gene Expression*
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Genetic Vectors
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Hepatocytes / cytology
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Hepatocytes / drug effects
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Humans
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Lipopolysaccharides / pharmacology*
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Lymphocyte Antigen 96
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Membrane Glycoproteins / genetics
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Membrane Glycoproteins / physiology*
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Mice
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Mice, Inbred C3H
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Mice, Inbred C57BL
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Mitogen-Activated Protein Kinase 1 / metabolism
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Mitogen-Activated Protein Kinase 3
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Mitogen-Activated Protein Kinases / metabolism
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Myeloid Differentiation Factor 88
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NF-kappa B / metabolism*
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Oligonucleotide Array Sequence Analysis
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Receptors, Cell Surface / genetics
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Receptors, Cell Surface / physiology*
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Receptors, Immunologic / genetics
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Signal Transduction*
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Toll-Like Receptor 1
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Toll-Like Receptor 4
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Toll-Like Receptor 9
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Toll-Like Receptors
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Transcription Factor AP-1 / metabolism
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Tumor Cells, Cultured
Substances
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Adaptor Proteins, Signal Transducing
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Antigens, Differentiation
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Antigens, Surface
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Drosophila Proteins
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LY96 protein, human
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Lipopolysaccharides
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Lymphocyte Antigen 96
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MYD88 protein, human
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Membrane Glycoproteins
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Myd88 protein, mouse
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Myeloid Differentiation Factor 88
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NF-kappa B
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Receptors, Cell Surface
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Receptors, Immunologic
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TLR4 protein, human
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TLR9 protein, human
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Toll-Like Receptor 1
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Toll-Like Receptor 4
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Toll-Like Receptor 9
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Toll-Like Receptors
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Transcription Factor AP-1
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Mitogen-Activated Protein Kinase 1
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Mitogen-Activated Protein Kinase 3
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Mitogen-Activated Protein Kinases