A Role for Class A Scavenger Receptor in Dendritic Cell Nibbling from Live Cells
Monocyte-derived dendritic cells (DC) possess the unique capacity to capture Ag from live cells through intimate cell contact, a process referred to as nibbling. We sought to define the receptor(s) mediating DC nibbling. Uptake of fluorescently labeled plasma membrane from live cells by DC was inhib...
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description | Monocyte-derived dendritic cells (DC) possess the unique capacity to capture Ag from live cells through intimate cell contact, a process referred to as nibbling. We sought to define the receptor(s) mediating DC nibbling. Uptake of fluorescently labeled plasma membrane from live cells by DC was inhibited by protease treatment and by a panel of polyanionic ligands, implicating scavenger receptors (SR) in this process. Differential expression of SR on DC and macrophages correlated with the capacity to acquire membrane from live cells. Internalized membrane colocalized with SR ligand and entered the endosomal pathway. DC very efficiently acquired and internalized gp100 tumor Ag expressed at the surface of viable adenocarcinoma cells via recombinant adenoviral infection. Cross-presentation of gp100 by DC to MHC class I-restricted T cells was inhibited by polyanionic SR ligand and an Ab to type A SR (SR-A), whereas Ab to the class B SR CD36, which mediates uptake of apoptotic cells, induced no inhibition. DC capture of fluorescently labeled membrane from live cells was partially blocked by SR-A-specific Ab, suggesting that other SR may also be contributing to nibbling. DC maturation resulted in a switch in expression from type II SR-A (SR-AII) to the SR-AI splice variant. Finally, SR-A was identified on interdigitating DC isolated from monkey lymph nodes. These findings define a novel role for SR-A, and suggest that Ag uptake from live cells by DC may be important in the generation of immunity and in the maintenance of peripheral tolerance in vivo. |
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We sought to define the receptor(s) mediating DC nibbling. Uptake of fluorescently labeled plasma membrane from live cells by DC was inhibited by protease treatment and by a panel of polyanionic ligands, implicating scavenger receptors (SR) in this process. Differential expression of SR on DC and macrophages correlated with the capacity to acquire membrane from live cells. Internalized membrane colocalized with SR ligand and entered the endosomal pathway. DC very efficiently acquired and internalized gp100 tumor Ag expressed at the surface of viable adenocarcinoma cells via recombinant adenoviral infection. Cross-presentation of gp100 by DC to MHC class I-restricted T cells was inhibited by polyanionic SR ligand and an Ab to type A SR (SR-A), whereas Ab to the class B SR CD36, which mediates uptake of apoptotic cells, induced no inhibition. DC capture of fluorescently labeled membrane from live cells was partially blocked by SR-A-specific Ab, suggesting that other SR may also be contributing to nibbling. DC maturation resulted in a switch in expression from type II SR-A (SR-AII) to the SR-AI splice variant. Finally, SR-A was identified on interdigitating DC isolated from monkey lymph nodes. 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We sought to define the receptor(s) mediating DC nibbling. Uptake of fluorescently labeled plasma membrane from live cells by DC was inhibited by protease treatment and by a panel of polyanionic ligands, implicating scavenger receptors (SR) in this process. Differential expression of SR on DC and macrophages correlated with the capacity to acquire membrane from live cells. Internalized membrane colocalized with SR ligand and entered the endosomal pathway. DC very efficiently acquired and internalized gp100 tumor Ag expressed at the surface of viable adenocarcinoma cells via recombinant adenoviral infection. Cross-presentation of gp100 by DC to MHC class I-restricted T cells was inhibited by polyanionic SR ligand and an Ab to type A SR (SR-A), whereas Ab to the class B SR CD36, which mediates uptake of apoptotic cells, induced no inhibition. DC capture of fluorescently labeled membrane from live cells was partially blocked by SR-A-specific Ab, suggesting that other SR may also be contributing to nibbling. DC maturation resulted in a switch in expression from type II SR-A (SR-AII) to the SR-AI splice variant. Finally, SR-A was identified on interdigitating DC isolated from monkey lymph nodes. These findings define a novel role for SR-A, and suggest that Ag uptake from live cells by DC may be important in the generation of immunity and in the maintenance of peripheral tolerance in vivo.</description><subject>Animals</subject><subject>Antigen Presentation - immunology</subject><subject>Antigens - metabolism</subject><subject>Antigens, Neoplasm - biosynthesis</subject><subject>Antigens, Neoplasm - metabolism</subject><subject>Binding, Competitive - immunology</subject><subject>Cell Communication - immunology</subject><subject>Cells, Cultured</subject><subject>Coculture Techniques</subject><subject>Dendritic Cells - immunology</subject><subject>Dendritic Cells - metabolism</subject><subject>Down-Regulation - immunology</subject><subject>gp100 Melanoma Antigen</subject><subject>Humans</subject><subject>Immune Sera - pharmacology</subject><subject>Ligands</subject><subject>Lymph Nodes - cytology</subject><subject>Lymph Nodes - immunology</subject><subject>Lymph Nodes - metabolism</subject><subject>Macaca mulatta</subject><subject>Mannans - metabolism</subject><subject>Mannans - pharmacology</subject><subject>Membrane Glycoproteins - biosynthesis</subject><subject>Membrane Glycoproteins - metabolism</subject><subject>Monocytes - immunology</subject><subject>Monocytes - metabolism</subject><subject>Neoplasm Proteins - biosynthesis</subject><subject>Neoplasm Proteins - metabolism</subject><subject>Oligopeptides - metabolism</subject><subject>Oligopeptides - pharmacology</subject><subject>Receptors, Immunologic - biosynthesis</subject><subject>Receptors, Immunologic - immunology</subject><subject>Receptors, Immunologic - metabolism</subject><subject>Receptors, Immunologic - physiology</subject><subject>Receptors, Scavenger</subject><subject>Scavenger Receptors, Class A</subject><subject>Subcellular Fractions - immunology</subject><subject>Subcellular Fractions - metabolism</subject><subject>Tumor Cells, Cultured</subject><issn>0022-1767</issn><issn>1550-6606</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1P20AQhlcIVELaX4CE9gQnh9lv-xilpVSKAEF7XtnrcdhobYfdmKj_vqYJKrdeZqSZZ16NHkLOGcwkyOJ67dt26PowYwZmasYF8CMyYUpBpjXoYzIB4DxjRptTcpbSGgA0cPmJnDKuCskVm5CHOX3sA9Kmj3QRypTonD658hW7FUb6iA4323HlO_oVuzr6rXd0gSHQO19VwXcr2sS-pUv_in_n6TM5acqQ8MuhT8mvm28_F7fZ8v77j8V8mTlp1DaTwhWiyHNUUrE8Z7U0HGrOxtIU0lRCaigE4wadNk1t6lJWquFc5yU6I7iYkst97ib2LwOmrW19cuMHZYf9kKwRIHPG2H9BlusClClGUOxBF_uUIjZ2E31bxt-WgX0zbt-N29G4VfbN-Hh1cYgfqhbrfzcHxSNwtQee_ep55yPa1JYhjDizu93uQ9QfE1aJaQ</recordid><startdate>20030301</startdate><enddate>20030301</enddate><creator>Harshyne, Larry A</creator><creator>Zimmer, Michael I</creator><creator>Watkins, Simon C</creator><creator>Barratt-Boyes, Simon M</creator><general>Am Assoc Immnol</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>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20030301</creationdate><title>A Role for Class A Scavenger Receptor in Dendritic Cell Nibbling from Live Cells</title><author>Harshyne, Larry A ; Zimmer, Michael I ; Watkins, Simon C ; Barratt-Boyes, Simon M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c475t-43c93988e5451881d4720d2120df947b346093127ec67fd7da4b5f2268aec7323</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Animals</topic><topic>Antigen Presentation - immunology</topic><topic>Antigens - metabolism</topic><topic>Antigens, Neoplasm - biosynthesis</topic><topic>Antigens, Neoplasm - metabolism</topic><topic>Binding, Competitive - immunology</topic><topic>Cell Communication - immunology</topic><topic>Cells, Cultured</topic><topic>Coculture Techniques</topic><topic>Dendritic Cells - immunology</topic><topic>Dendritic Cells - metabolism</topic><topic>Down-Regulation - immunology</topic><topic>gp100 Melanoma Antigen</topic><topic>Humans</topic><topic>Immune Sera - pharmacology</topic><topic>Ligands</topic><topic>Lymph Nodes - cytology</topic><topic>Lymph Nodes - immunology</topic><topic>Lymph Nodes - metabolism</topic><topic>Macaca mulatta</topic><topic>Mannans - metabolism</topic><topic>Mannans - pharmacology</topic><topic>Membrane Glycoproteins - biosynthesis</topic><topic>Membrane Glycoproteins - metabolism</topic><topic>Monocytes - immunology</topic><topic>Monocytes - metabolism</topic><topic>Neoplasm Proteins - biosynthesis</topic><topic>Neoplasm Proteins - metabolism</topic><topic>Oligopeptides - metabolism</topic><topic>Oligopeptides - pharmacology</topic><topic>Receptors, Immunologic - biosynthesis</topic><topic>Receptors, Immunologic - immunology</topic><topic>Receptors, Immunologic - metabolism</topic><topic>Receptors, Immunologic - physiology</topic><topic>Receptors, Scavenger</topic><topic>Scavenger Receptors, Class A</topic><topic>Subcellular Fractions - immunology</topic><topic>Subcellular Fractions - metabolism</topic><topic>Tumor Cells, Cultured</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Harshyne, Larry A</creatorcontrib><creatorcontrib>Zimmer, Michael I</creatorcontrib><creatorcontrib>Watkins, Simon C</creatorcontrib><creatorcontrib>Barratt-Boyes, Simon M</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of immunology (1950)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Harshyne, Larry A</au><au>Zimmer, Michael I</au><au>Watkins, Simon C</au><au>Barratt-Boyes, Simon M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Role for Class A Scavenger Receptor in Dendritic Cell Nibbling from Live Cells</atitle><jtitle>The Journal of immunology (1950)</jtitle><addtitle>J Immunol</addtitle><date>2003-03-01</date><risdate>2003</risdate><volume>170</volume><issue>5</issue><spage>2302</spage><epage>2309</epage><pages>2302-2309</pages><issn>0022-1767</issn><eissn>1550-6606</eissn><abstract>Monocyte-derived dendritic cells (DC) possess the unique capacity to capture Ag from live cells through intimate cell contact, a process referred to as nibbling. We sought to define the receptor(s) mediating DC nibbling. Uptake of fluorescently labeled plasma membrane from live cells by DC was inhibited by protease treatment and by a panel of polyanionic ligands, implicating scavenger receptors (SR) in this process. Differential expression of SR on DC and macrophages correlated with the capacity to acquire membrane from live cells. Internalized membrane colocalized with SR ligand and entered the endosomal pathway. DC very efficiently acquired and internalized gp100 tumor Ag expressed at the surface of viable adenocarcinoma cells via recombinant adenoviral infection. Cross-presentation of gp100 by DC to MHC class I-restricted T cells was inhibited by polyanionic SR ligand and an Ab to type A SR (SR-A), whereas Ab to the class B SR CD36, which mediates uptake of apoptotic cells, induced no inhibition. DC capture of fluorescently labeled membrane from live cells was partially blocked by SR-A-specific Ab, suggesting that other SR may also be contributing to nibbling. DC maturation resulted in a switch in expression from type II SR-A (SR-AII) to the SR-AI splice variant. Finally, SR-A was identified on interdigitating DC isolated from monkey lymph nodes. These findings define a novel role for SR-A, and suggest that Ag uptake from live cells by DC may be important in the generation of immunity and in the maintenance of peripheral tolerance in vivo.</abstract><cop>United States</cop><pub>Am Assoc Immnol</pub><pmid>12594251</pmid><doi>10.4049/jimmunol.170.5.2302</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antigen Presentation - immunology Antigens - metabolism Antigens, Neoplasm - biosynthesis Antigens, Neoplasm - metabolism Binding, Competitive - immunology Cell Communication - immunology Cells, Cultured Coculture Techniques Dendritic Cells - immunology Dendritic Cells - metabolism Down-Regulation - immunology gp100 Melanoma Antigen Humans Immune Sera - pharmacology Ligands Lymph Nodes - cytology Lymph Nodes - immunology Lymph Nodes - metabolism Macaca mulatta Mannans - metabolism Mannans - pharmacology Membrane Glycoproteins - biosynthesis Membrane Glycoproteins - metabolism Monocytes - immunology Monocytes - metabolism Neoplasm Proteins - biosynthesis Neoplasm Proteins - metabolism Oligopeptides - metabolism Oligopeptides - pharmacology Receptors, Immunologic - biosynthesis Receptors, Immunologic - immunology Receptors, Immunologic - metabolism Receptors, Immunologic - physiology Receptors, Scavenger Scavenger Receptors, Class A Subcellular Fractions - immunology Subcellular Fractions - metabolism Tumor Cells, Cultured |
title | A Role for Class A Scavenger Receptor in Dendritic Cell Nibbling from Live Cells |
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