Regulation and Signal Transduction of Toll-Like Receptors in Human Chorioncarcinoma Cell Lines

Problem:  Toll‐like receptors (TLRs) are expressed on placental cells. The aim of this study is to analyze signaling components activated in placenta cells after TLR ligand engagement. Methods of study:  In chorioncarcimoma cell lines the regulation of TLRs was determined by real time polymerase cha...

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Veröffentlicht in:American journal of reproductive immunology (1989) 2005-02, Vol.53 (2), p.77-84
Hauptverfasser: Klaffenbach, Daniela, Rascher, Wolfgang, Röllinghoff, Martin, Dötsch, Jörg, Meißner, Udo, Schnare, Markus
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container_issue 2
container_start_page 77
container_title American journal of reproductive immunology (1989)
container_volume 53
creator Klaffenbach, Daniela
Rascher, Wolfgang
Röllinghoff, Martin
Dötsch, Jörg
Meißner, Udo
Schnare, Markus
description Problem:  Toll‐like receptors (TLRs) are expressed on placental cells. The aim of this study is to analyze signaling components activated in placenta cells after TLR ligand engagement. Methods of study:  In chorioncarcimoma cell lines the regulation of TLRs was determined by real time polymerase chain reaction as well as by fluorescence‐activated cell sorter analysis. Activation of NF‐κB was determined in a reporter assay system and the activation of the mitogen‐activated protein kinase signaling pathways by immunoblot analysis. Results:  Both lipopolysaccharide (LPS) and DNA oligonucleotides containing unmethylated CpG motifs (CpG) induced the enhanced expression of TLR2 mRNA as well as a TLR2 surface protein expression. Functionally, incubation of JAR cells with microbial stimuli such as LPS activated NF‐κB, as well as the phosphorylation of ERK1/2 and p38 MAP kinases and secretion of interleukin‐8. Conclusion:  The functional expression of TLRs on placental cells may play an important role in the initiation of an immune response in the developing fetus.
doi_str_mv 10.1111/j.1600-0897.2004.00247.x
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The aim of this study is to analyze signaling components activated in placenta cells after TLR ligand engagement. Methods of study:  In chorioncarcimoma cell lines the regulation of TLRs was determined by real time polymerase chain reaction as well as by fluorescence‐activated cell sorter analysis. Activation of NF‐κB was determined in a reporter assay system and the activation of the mitogen‐activated protein kinase signaling pathways by immunoblot analysis. Results:  Both lipopolysaccharide (LPS) and DNA oligonucleotides containing unmethylated CpG motifs (CpG) induced the enhanced expression of TLR2 mRNA as well as a TLR2 surface protein expression. Functionally, incubation of JAR cells with microbial stimuli such as LPS activated NF‐κB, as well as the phosphorylation of ERK1/2 and p38 MAP kinases and secretion of interleukin‐8. 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The aim of this study is to analyze signaling components activated in placenta cells after TLR ligand engagement. Methods of study:  In chorioncarcimoma cell lines the regulation of TLRs was determined by real time polymerase chain reaction as well as by fluorescence‐activated cell sorter analysis. Activation of NF‐κB was determined in a reporter assay system and the activation of the mitogen‐activated protein kinase signaling pathways by immunoblot analysis. Results:  Both lipopolysaccharide (LPS) and DNA oligonucleotides containing unmethylated CpG motifs (CpG) induced the enhanced expression of TLR2 mRNA as well as a TLR2 surface protein expression. Functionally, incubation of JAR cells with microbial stimuli such as LPS activated NF‐κB, as well as the phosphorylation of ERK1/2 and p38 MAP kinases and secretion of interleukin‐8. Conclusion:  The functional expression of TLRs on placental cells may play an important role in the initiation of an immune response in the developing fetus.</description><subject>Cell Line, Tumor</subject><subject>Choriocarcinoma - genetics</subject><subject>Choriocarcinoma - immunology</subject><subject>Female</subject><subject>Gene Expression Regulation</subject><subject>Humans</subject><subject>Innate immune response</subject><subject>Interleukin-8 - immunology</subject><subject>Lipopolysaccharides - pharmacology</subject><subject>Membrane Glycoproteins - drug effects</subject><subject>Membrane Glycoproteins - genetics</subject><subject>Membrane Glycoproteins - immunology</subject><subject>mitogen-activated protein kinase</subject><subject>Mitogen-Activated Protein Kinases - metabolism</subject><subject>NF-kappa B - metabolism</subject><subject>NF-κB</subject><subject>Oligonucleotides - pharmacology</subject><subject>placenta</subject><subject>Placenta - cytology</subject><subject>Placenta - immunology</subject><subject>Pregnancy</subject><subject>Receptors, Cell Surface - drug effects</subject><subject>Receptors, Cell Surface - genetics</subject><subject>Receptors, Cell Surface - immunology</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>RNA, Messenger - drug effects</subject><subject>RNA, Messenger - genetics</subject><subject>Signal Transduction - immunology</subject><subject>Toll-Like Receptor 2</subject><subject>Toll-Like Receptors</subject><subject>Trophoblasts - immunology</subject><issn>1046-7408</issn><issn>1600-0897</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkFFP2zAUha0JNBjwFyY_8ZbMiZ04kXhBFbRU0ZBoJ3jCsp0b5pLYxW608u_n0oq9zi--uj7fvccHIZyRNIvnxyrNSkISUtU8zQlhKSE54-n2Czr9fDiKNWFlwhmpTtC3EFaExD7lX9FJVvCaUJadoucHeBl7uTHOYmlbvDAvVvZ46aUN7ag_-q7DS9f3SWNeAT-AhvXG-YCNxbNxkBZPfjsfdVp6bawbJJ5A3-PGWAjn6LiTfYCLw32Gft3eLCezpLmf3k2um0QzTnj0yHItAeqO0rpQsspkycq6kLRQTBWKct6BAk4UKJK3tGW1BF5rWoLKs0idocv93LV3byOEjRhM0NGGtODGIEpeFPG_VRRWe6H2LgQPnVh7M0j_LjIidtmKldhFKHYRil224iNbsY3o98OOUQ3Q_gMPYUbB1V7wx_Tw_t-DxfX8LhYRT_a4CRvYfuLSv0b7lBfi8edUNIvHxfxpNhdT-heAxJen</recordid><startdate>200502</startdate><enddate>200502</enddate><creator>Klaffenbach, Daniela</creator><creator>Rascher, Wolfgang</creator><creator>Röllinghoff, Martin</creator><creator>Dötsch, Jörg</creator><creator>Meißner, Udo</creator><creator>Schnare, Markus</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>200502</creationdate><title>Regulation and Signal Transduction of Toll-Like Receptors in Human Chorioncarcinoma Cell Lines</title><author>Klaffenbach, Daniela ; 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The aim of this study is to analyze signaling components activated in placenta cells after TLR ligand engagement. Methods of study:  In chorioncarcimoma cell lines the regulation of TLRs was determined by real time polymerase chain reaction as well as by fluorescence‐activated cell sorter analysis. Activation of NF‐κB was determined in a reporter assay system and the activation of the mitogen‐activated protein kinase signaling pathways by immunoblot analysis. Results:  Both lipopolysaccharide (LPS) and DNA oligonucleotides containing unmethylated CpG motifs (CpG) induced the enhanced expression of TLR2 mRNA as well as a TLR2 surface protein expression. Functionally, incubation of JAR cells with microbial stimuli such as LPS activated NF‐κB, as well as the phosphorylation of ERK1/2 and p38 MAP kinases and secretion of interleukin‐8. 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subjects Cell Line, Tumor
Choriocarcinoma - genetics
Choriocarcinoma - immunology
Female
Gene Expression Regulation
Humans
Innate immune response
Interleukin-8 - immunology
Lipopolysaccharides - pharmacology
Membrane Glycoproteins - drug effects
Membrane Glycoproteins - genetics
Membrane Glycoproteins - immunology
mitogen-activated protein kinase
Mitogen-Activated Protein Kinases - metabolism
NF-kappa B - metabolism
NF-κB
Oligonucleotides - pharmacology
placenta
Placenta - cytology
Placenta - immunology
Pregnancy
Receptors, Cell Surface - drug effects
Receptors, Cell Surface - genetics
Receptors, Cell Surface - immunology
Reverse Transcriptase Polymerase Chain Reaction
RNA, Messenger - drug effects
RNA, Messenger - genetics
Signal Transduction - immunology
Toll-Like Receptor 2
Toll-Like Receptors
Trophoblasts - immunology
title Regulation and Signal Transduction of Toll-Like Receptors in Human Chorioncarcinoma Cell Lines
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