Constitutive interaction between 4-1BB and 4-1BBL on murine LPS-activated bone marrow dendritic cells masks detection of 4-1BBL by TKS-1 but not 19H3 antibody

4-1BB is a TNFR family member associated with NF-κB mediated survival signaling. 4-1BB is widely expressed on activated cells of the immune system, including activated T cells, NK cells and dendritic cells. Its ligand, 4-1BBL, is transiently expressed on activated antigen presenting cells and at low...

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Veröffentlicht in:Journal of immunological methods 2017-11, Vol.450, p.81-89
Hauptverfasser: Mbanwi, Achire N., Lin, Gloria H.Y., Wang, Kuan Chung, Watts, Tania H.
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Lin, Gloria H.Y.
Wang, Kuan Chung
Watts, Tania H.
description 4-1BB is a TNFR family member associated with NF-κB mediated survival signaling. 4-1BB is widely expressed on activated cells of the immune system, including activated T cells, NK cells and dendritic cells. Its ligand, 4-1BBL, is transiently expressed on activated antigen presenting cells and at low levels on activated T cells. Although 4-1BBL-deficient mice clearly demonstrate a role for 4-1BBL in CD8 T cell responses to viruses such as influenza, 4-1BBL can be difficult to detect following infection of mice. Here we provide evidence for a constitutive interaction between endogenous 4-1BB and 4-1BBL on LPS activated bone marrow-derived murine dendritic cells that can mask its detection, with implications for measurement of 4-1BBL expression. The masking of 4-1BBL by its receptor results in loss of reactivity to the anti-4-1BBL antibody TKS-1, whereas the 19H3 antibody binds to 4-1BBL in the presence or absence of 4-1BB. Moreover, 4-1BB/4-1BBL interaction can occur in trans between 4-1BB+/+ and 4-1BB−/− dendritic cells in culture. These data suggest that 19H3 is the preferable antibody to use to detect 4-1BBL in the presence of its receptor. [Display omitted] •The anti-4-1BBL antibodies TKS-1 and 19H3 bind to distinct sites on 4-1BBL.•The TKS-1 but not the 19H3 antibody binding site on 4-1BBL is masked by 4-1BB.•4-1BB can bind to 4-1BBL on an adjacent DC to block TKS-1 binding in trans.•4-1BB and 4-1BBL interact constitutively on LPS-activated bone marrow derived DC.•19H3 is the preferred antibody to use to detect 4-1BBL when 4-1BB is present.
doi_str_mv 10.1016/j.jim.2017.08.001
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Its ligand, 4-1BBL, is transiently expressed on activated antigen presenting cells and at low levels on activated T cells. Although 4-1BBL-deficient mice clearly demonstrate a role for 4-1BBL in CD8 T cell responses to viruses such as influenza, 4-1BBL can be difficult to detect following infection of mice. Here we provide evidence for a constitutive interaction between endogenous 4-1BB and 4-1BBL on LPS activated bone marrow-derived murine dendritic cells that can mask its detection, with implications for measurement of 4-1BBL expression. The masking of 4-1BBL by its receptor results in loss of reactivity to the anti-4-1BBL antibody TKS-1, whereas the 19H3 antibody binds to 4-1BBL in the presence or absence of 4-1BB. Moreover, 4-1BB/4-1BBL interaction can occur in trans between 4-1BB+/+ and 4-1BB−/− dendritic cells in culture. These data suggest that 19H3 is the preferable antibody to use to detect 4-1BBL in the presence of its receptor. [Display omitted] •The anti-4-1BBL antibodies TKS-1 and 19H3 bind to distinct sites on 4-1BBL.•The TKS-1 but not the 19H3 antibody binding site on 4-1BBL is masked by 4-1BB.•4-1BB can bind to 4-1BBL on an adjacent DC to block TKS-1 binding in trans.•4-1BB and 4-1BBL interact constitutively on LPS-activated bone marrow derived DC.•19H3 is the preferred antibody to use to detect 4-1BBL when 4-1BB is present.</description><identifier>ISSN: 0022-1759</identifier><identifier>EISSN: 1872-7905</identifier><identifier>DOI: 10.1016/j.jim.2017.08.001</identifier><identifier>PMID: 28789924</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>19H3 ; 4-1BB ; 4-1BB Ligand - genetics ; 4-1BB Ligand - immunology ; 4-1BB Ligand - metabolism ; 4-1BBL ; Animals ; Antibodies - immunology ; Antibody blocking ; Antibody Specificity ; Bone Marrow Cells - drug effects ; Bone Marrow Cells - immunology ; Bone Marrow Cells - metabolism ; Cell Separation - methods ; Cells, Cultured ; Dendritic cells ; Dendritic Cells - drug effects ; Dendritic Cells - immunology ; Dendritic Cells - metabolism ; Epitopes ; Flow Cytometry ; Genotype ; Lipopolysaccharides - pharmacology ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Phenotype ; Protein Binding ; Reproducibility of Results ; TKS-1 ; Tumor Necrosis Factor Receptor Superfamily, Member 9 - genetics ; Tumor Necrosis Factor Receptor Superfamily, Member 9 - immunology ; Tumor Necrosis Factor Receptor Superfamily, Member 9 - metabolism</subject><ispartof>Journal of immunological methods, 2017-11, Vol.450, p.81-89</ispartof><rights>2017 Elsevier B.V.</rights><rights>Copyright © 2017 Elsevier B.V. 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[Display omitted] •The anti-4-1BBL antibodies TKS-1 and 19H3 bind to distinct sites on 4-1BBL.•The TKS-1 but not the 19H3 antibody binding site on 4-1BBL is masked by 4-1BB.•4-1BB can bind to 4-1BBL on an adjacent DC to block TKS-1 binding in trans.•4-1BB and 4-1BBL interact constitutively on LPS-activated bone marrow derived DC.•19H3 is the preferred antibody to use to detect 4-1BBL when 4-1BB is present.</description><subject>19H3</subject><subject>4-1BB</subject><subject>4-1BB Ligand - genetics</subject><subject>4-1BB Ligand - immunology</subject><subject>4-1BB Ligand - metabolism</subject><subject>4-1BBL</subject><subject>Animals</subject><subject>Antibodies - immunology</subject><subject>Antibody blocking</subject><subject>Antibody Specificity</subject><subject>Bone Marrow Cells - drug effects</subject><subject>Bone Marrow Cells - immunology</subject><subject>Bone Marrow Cells - metabolism</subject><subject>Cell Separation - methods</subject><subject>Cells, Cultured</subject><subject>Dendritic cells</subject><subject>Dendritic Cells - drug effects</subject><subject>Dendritic Cells - immunology</subject><subject>Dendritic Cells - metabolism</subject><subject>Epitopes</subject><subject>Flow Cytometry</subject><subject>Genotype</subject><subject>Lipopolysaccharides - pharmacology</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Knockout</subject><subject>Phenotype</subject><subject>Protein Binding</subject><subject>Reproducibility of Results</subject><subject>TKS-1</subject><subject>Tumor Necrosis Factor Receptor Superfamily, Member 9 - genetics</subject><subject>Tumor Necrosis Factor Receptor Superfamily, Member 9 - immunology</subject><subject>Tumor Necrosis Factor Receptor Superfamily, Member 9 - metabolism</subject><issn>0022-1759</issn><issn>1872-7905</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc2OFCEUhYnROO3oA7gxLN1UCVRRVMWV0xkdYyeazLgm_FwS2i4YgepJv4zPKp2acWlCAjl898C9B6G3lLSU0OHDvt37uWWEipaMLSH0GdrQUbBGTIQ_RxtCGGuo4NMFepXznlSCDOQlumCjGKeJ9Rv0ZxtDLr4sxR8B-1AgKVN8DFhDeQAIuG_o1RVWwa6nHa5385J8ALz7cduc6aMqYLGOVZpVSvEBWwg2-eINNnA45CrnX7mqBVbz6J7c9AnffbttKNZLwSEWTKebrj5XvI729Bq9cOqQ4c3jfol-fr6-2940u-9fvm4_7RrT8a401Nqpm7gamVM9p051GobeWs6UsxzESASjPR-4mJhw1vWGkGGsa9BGd053l-j96nuf4u8FcpGzz-evqwBxyZLWOj71nPQVpStqUsw5gZP3yde2T5ISeY5F7mWNRZ5jkWSUdei15t2j_aJnsP8qnnKowMcVgNrk0UOS2XgIBqxPdWTSRv8f-79LPpxE</recordid><startdate>201711</startdate><enddate>201711</enddate><creator>Mbanwi, Achire N.</creator><creator>Lin, Gloria H.Y.</creator><creator>Wang, Kuan Chung</creator><creator>Watts, Tania H.</creator><general>Elsevier B.V</general><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>201711</creationdate><title>Constitutive interaction between 4-1BB and 4-1BBL on murine LPS-activated bone marrow dendritic cells masks detection of 4-1BBL by TKS-1 but not 19H3 antibody</title><author>Mbanwi, Achire N. ; Lin, Gloria H.Y. ; Wang, Kuan Chung ; Watts, Tania H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c353t-1dd9395a82fa451fa3be64dd52afd5e78072145657927fdf4c00680686bcb3fb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>19H3</topic><topic>4-1BB</topic><topic>4-1BB Ligand - genetics</topic><topic>4-1BB Ligand - immunology</topic><topic>4-1BB Ligand - metabolism</topic><topic>4-1BBL</topic><topic>Animals</topic><topic>Antibodies - immunology</topic><topic>Antibody blocking</topic><topic>Antibody Specificity</topic><topic>Bone Marrow Cells - drug effects</topic><topic>Bone Marrow Cells - immunology</topic><topic>Bone Marrow Cells - metabolism</topic><topic>Cell Separation - methods</topic><topic>Cells, Cultured</topic><topic>Dendritic cells</topic><topic>Dendritic Cells - drug effects</topic><topic>Dendritic Cells - immunology</topic><topic>Dendritic Cells - metabolism</topic><topic>Epitopes</topic><topic>Flow Cytometry</topic><topic>Genotype</topic><topic>Lipopolysaccharides - pharmacology</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Knockout</topic><topic>Phenotype</topic><topic>Protein Binding</topic><topic>Reproducibility of Results</topic><topic>TKS-1</topic><topic>Tumor Necrosis Factor Receptor Superfamily, Member 9 - genetics</topic><topic>Tumor Necrosis Factor Receptor Superfamily, Member 9 - immunology</topic><topic>Tumor Necrosis Factor Receptor Superfamily, Member 9 - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mbanwi, Achire N.</creatorcontrib><creatorcontrib>Lin, Gloria H.Y.</creatorcontrib><creatorcontrib>Wang, Kuan Chung</creatorcontrib><creatorcontrib>Watts, Tania H.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of immunological methods</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mbanwi, Achire N.</au><au>Lin, Gloria H.Y.</au><au>Wang, Kuan Chung</au><au>Watts, Tania H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Constitutive interaction between 4-1BB and 4-1BBL on murine LPS-activated bone marrow dendritic cells masks detection of 4-1BBL by TKS-1 but not 19H3 antibody</atitle><jtitle>Journal of immunological methods</jtitle><addtitle>J Immunol Methods</addtitle><date>2017-11</date><risdate>2017</risdate><volume>450</volume><spage>81</spage><epage>89</epage><pages>81-89</pages><issn>0022-1759</issn><eissn>1872-7905</eissn><abstract>4-1BB is a TNFR family member associated with NF-κB mediated survival signaling. 4-1BB is widely expressed on activated cells of the immune system, including activated T cells, NK cells and dendritic cells. Its ligand, 4-1BBL, is transiently expressed on activated antigen presenting cells and at low levels on activated T cells. Although 4-1BBL-deficient mice clearly demonstrate a role for 4-1BBL in CD8 T cell responses to viruses such as influenza, 4-1BBL can be difficult to detect following infection of mice. Here we provide evidence for a constitutive interaction between endogenous 4-1BB and 4-1BBL on LPS activated bone marrow-derived murine dendritic cells that can mask its detection, with implications for measurement of 4-1BBL expression. The masking of 4-1BBL by its receptor results in loss of reactivity to the anti-4-1BBL antibody TKS-1, whereas the 19H3 antibody binds to 4-1BBL in the presence or absence of 4-1BB. Moreover, 4-1BB/4-1BBL interaction can occur in trans between 4-1BB+/+ and 4-1BB−/− dendritic cells in culture. These data suggest that 19H3 is the preferable antibody to use to detect 4-1BBL in the presence of its receptor. [Display omitted] •The anti-4-1BBL antibodies TKS-1 and 19H3 bind to distinct sites on 4-1BBL.•The TKS-1 but not the 19H3 antibody binding site on 4-1BBL is masked by 4-1BB.•4-1BB can bind to 4-1BBL on an adjacent DC to block TKS-1 binding in trans.•4-1BB and 4-1BBL interact constitutively on LPS-activated bone marrow derived DC.•19H3 is the preferred antibody to use to detect 4-1BBL when 4-1BB is present.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>28789924</pmid><doi>10.1016/j.jim.2017.08.001</doi><tpages>9</tpages></addata></record>
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subjects 19H3
4-1BB
4-1BB Ligand - genetics
4-1BB Ligand - immunology
4-1BB Ligand - metabolism
4-1BBL
Animals
Antibodies - immunology
Antibody blocking
Antibody Specificity
Bone Marrow Cells - drug effects
Bone Marrow Cells - immunology
Bone Marrow Cells - metabolism
Cell Separation - methods
Cells, Cultured
Dendritic cells
Dendritic Cells - drug effects
Dendritic Cells - immunology
Dendritic Cells - metabolism
Epitopes
Flow Cytometry
Genotype
Lipopolysaccharides - pharmacology
Mice
Mice, Inbred C57BL
Mice, Knockout
Phenotype
Protein Binding
Reproducibility of Results
TKS-1
Tumor Necrosis Factor Receptor Superfamily, Member 9 - genetics
Tumor Necrosis Factor Receptor Superfamily, Member 9 - immunology
Tumor Necrosis Factor Receptor Superfamily, Member 9 - metabolism
title Constitutive interaction between 4-1BB and 4-1BBL on murine LPS-activated bone marrow dendritic cells masks detection of 4-1BBL by TKS-1 but not 19H3 antibody
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