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Lipid Protein Interactions: The Assembly of CD1d1 with Cellular Phospholipids Occurs in the Endoplasmic Reticulum
CD1d1 is a member of a family of lipid Ag-presenting molecules. The cellular ligands associated with CD1d1 were isolated and characterized by biochemical means as an approach to elucidate the mechanism by which CD1 molecules assemble in vivo. Natural ligands of mouse CD1d1 included cellular phosphat...
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Published in: | The Journal of immunology (1950) 2002-01, Vol.168 (2), p.723-733 |
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container_title | The Journal of immunology (1950) |
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creator | De Silva, A. Dharshan Park, J.-June Matsuki, Naoto Stanic, Aleksandar K Brutkiewicz, Randy R Medof, M. Edward Joyce, Sebastian |
description | CD1d1 is a member of a family of lipid Ag-presenting molecules. The cellular ligands associated with CD1d1 were isolated and characterized by biochemical means as an approach to elucidate the mechanism by which CD1 molecules assemble in vivo. Natural ligands of mouse CD1d1 included cellular phosphatidylinositol and phosphatidylinositol-glycans that are synthesized in the endoplasmic reticulum. Further biochemical data revealed that the two CD1d1 mutants, one defective in recycling from-and-to the plasma membrane and the other in efficiently negotiating the secretory pathway, associated with phosphatidylinositol. Thus phosphatidylinositol associated with CD1d1 in the early secretory pathway. Phosphatidylinositol also associated with CD1d1 in Pig-A-deficient cells that are defective in the first glycosylation step of glycosylphosphatidylinositol biosynthesis. Moreover, cellular phosphatidylinositol-glycans are not Valpha14Jalpha15 natural T cell Ags. Therefore, we predict that cellular lipids occlude the hydrophobic Ag-binding groove of CD1 during assembly until they are exchanged for a glycolipid Ag(s) within the recycling compartment for display on the plasma membrane. In this manner, cellular lipids might play a chaperone-like role in the assembly of CD1d1 in vivo, akin to the function of invariant chain in MHC class II assembly. |
doi_str_mv | 10.4049/jimmunol.168.2.723 |
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Dharshan ; Park, J.-June ; Matsuki, Naoto ; Stanic, Aleksandar K ; Brutkiewicz, Randy R ; Medof, M. Edward ; Joyce, Sebastian</creator><creatorcontrib>De Silva, A. Dharshan ; Park, J.-June ; Matsuki, Naoto ; Stanic, Aleksandar K ; Brutkiewicz, Randy R ; Medof, M. Edward ; Joyce, Sebastian</creatorcontrib><description>CD1d1 is a member of a family of lipid Ag-presenting molecules. The cellular ligands associated with CD1d1 were isolated and characterized by biochemical means as an approach to elucidate the mechanism by which CD1 molecules assemble in vivo. Natural ligands of mouse CD1d1 included cellular phosphatidylinositol and phosphatidylinositol-glycans that are synthesized in the endoplasmic reticulum. Further biochemical data revealed that the two CD1d1 mutants, one defective in recycling from-and-to the plasma membrane and the other in efficiently negotiating the secretory pathway, associated with phosphatidylinositol. Thus phosphatidylinositol associated with CD1d1 in the early secretory pathway. Phosphatidylinositol also associated with CD1d1 in Pig-A-deficient cells that are defective in the first glycosylation step of glycosylphosphatidylinositol biosynthesis. Moreover, cellular phosphatidylinositol-glycans are not Valpha14Jalpha15 natural T cell Ags. Therefore, we predict that cellular lipids occlude the hydrophobic Ag-binding groove of CD1 during assembly until they are exchanged for a glycolipid Ag(s) within the recycling compartment for display on the plasma membrane. In this manner, cellular lipids might play a chaperone-like role in the assembly of CD1d1 in vivo, akin to the function of invariant chain in MHC class II assembly.</description><identifier>ISSN: 0022-1767</identifier><identifier>EISSN: 1550-6606</identifier><identifier>DOI: 10.4049/jimmunol.168.2.723</identifier><identifier>PMID: 11777966</identifier><language>eng</language><publisher>United States: Am Assoc Immnol</publisher><subject>Animals ; Antigen Presentation ; Antigens, CD1 - metabolism ; Antigens, CD1d ; CD1d1 antigen ; Dolichol Phosphates - metabolism ; Endoplasmic Reticulum - enzymology ; Endoplasmic Reticulum - immunology ; Endoplasmic Reticulum - metabolism ; Glycosylphosphatidylinositols - deficiency ; Glycosylphosphatidylinositols - genetics ; Glycosylphosphatidylinositols - metabolism ; Humans ; Intracellular Fluid - immunology ; Intracellular Fluid - metabolism ; K562 Cells ; Ligands ; Mannose - metabolism ; Mice ; Phosphatidylethanolamines - metabolism ; phosphatidylinositol ; Phosphatidylinositol Diacylglycerol-Lyase ; Phosphatidylinositols - metabolism ; Phospholipids - metabolism ; Polysaccharides - metabolism ; Tumor Cells, Cultured ; Type C Phospholipases - metabolism</subject><ispartof>The Journal of immunology (1950), 2002-01, Vol.168 (2), p.723-733</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c405t-b6e2dc184469193e66b00c2236b3d2b893358081ede12de0fe5bc02517c9bf93</citedby><cites>FETCH-LOGICAL-c405t-b6e2dc184469193e66b00c2236b3d2b893358081ede12de0fe5bc02517c9bf93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11777966$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>De Silva, A. Dharshan</creatorcontrib><creatorcontrib>Park, J.-June</creatorcontrib><creatorcontrib>Matsuki, Naoto</creatorcontrib><creatorcontrib>Stanic, Aleksandar K</creatorcontrib><creatorcontrib>Brutkiewicz, Randy R</creatorcontrib><creatorcontrib>Medof, M. Edward</creatorcontrib><creatorcontrib>Joyce, Sebastian</creatorcontrib><title>Lipid Protein Interactions: The Assembly of CD1d1 with Cellular Phospholipids Occurs in the Endoplasmic Reticulum</title><title>The Journal of immunology (1950)</title><addtitle>J Immunol</addtitle><description>CD1d1 is a member of a family of lipid Ag-presenting molecules. The cellular ligands associated with CD1d1 were isolated and characterized by biochemical means as an approach to elucidate the mechanism by which CD1 molecules assemble in vivo. Natural ligands of mouse CD1d1 included cellular phosphatidylinositol and phosphatidylinositol-glycans that are synthesized in the endoplasmic reticulum. Further biochemical data revealed that the two CD1d1 mutants, one defective in recycling from-and-to the plasma membrane and the other in efficiently negotiating the secretory pathway, associated with phosphatidylinositol. Thus phosphatidylinositol associated with CD1d1 in the early secretory pathway. Phosphatidylinositol also associated with CD1d1 in Pig-A-deficient cells that are defective in the first glycosylation step of glycosylphosphatidylinositol biosynthesis. Moreover, cellular phosphatidylinositol-glycans are not Valpha14Jalpha15 natural T cell Ags. Therefore, we predict that cellular lipids occlude the hydrophobic Ag-binding groove of CD1 during assembly until they are exchanged for a glycolipid Ag(s) within the recycling compartment for display on the plasma membrane. In this manner, cellular lipids might play a chaperone-like role in the assembly of CD1d1 in vivo, akin to the function of invariant chain in MHC class II assembly.</description><subject>Animals</subject><subject>Antigen Presentation</subject><subject>Antigens, CD1 - metabolism</subject><subject>Antigens, CD1d</subject><subject>CD1d1 antigen</subject><subject>Dolichol Phosphates - metabolism</subject><subject>Endoplasmic Reticulum - enzymology</subject><subject>Endoplasmic Reticulum - immunology</subject><subject>Endoplasmic Reticulum - metabolism</subject><subject>Glycosylphosphatidylinositols - deficiency</subject><subject>Glycosylphosphatidylinositols - genetics</subject><subject>Glycosylphosphatidylinositols - metabolism</subject><subject>Humans</subject><subject>Intracellular Fluid - immunology</subject><subject>Intracellular Fluid - metabolism</subject><subject>K562 Cells</subject><subject>Ligands</subject><subject>Mannose - metabolism</subject><subject>Mice</subject><subject>Phosphatidylethanolamines - metabolism</subject><subject>phosphatidylinositol</subject><subject>Phosphatidylinositol Diacylglycerol-Lyase</subject><subject>Phosphatidylinositols - metabolism</subject><subject>Phospholipids - metabolism</subject><subject>Polysaccharides - metabolism</subject><subject>Tumor Cells, Cultured</subject><subject>Type C Phospholipases - metabolism</subject><issn>0022-1767</issn><issn>1550-6606</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNqFkcFq3DAQhkVoSLZpX6CHolNv3mokW7J7C5u0DSwkhL0LWx7XCpLlSDYmb18v2bLHnuby_98M8xHyBdg2Z3n1_cV6Pw_BbUGWW75VXFyQDRQFy6Rk8gPZMMZ5Bkqqa_IxpRfGmGQ8vyLXAEqpSsoNed3b0bb0KYYJ7UAfhgljbSYbhvSDHnqktymhb9wbDR3d3UELdLFTT3fo3OzqSJ_6kMY-uCMm0Udj5pjoSprW7v3QhtHVyVtDn3GyZnaz_0Quu9ol_HyaN-Tw8_6w-53tH3897G73mclZMWWNRN4aKPNcVlAJlLJhzHAuZCNa3pSVEEXJSsAWgbfIOiwaw3gBylRNV4kb8u0dO8bwOmOatLfJrFfXA4Y5aQVi_ZQS_w1CyUXF-ZHI34MmhpQidnqM1tfxTQPTRyH6nxC9CtFcr0LW0tcTfW48tufKycB5fW__9IuNqJOvnVvjoJdlOZP-Agmolsk</recordid><startdate>20020115</startdate><enddate>20020115</enddate><creator>De Silva, A. Dharshan</creator><creator>Park, J.-June</creator><creator>Matsuki, Naoto</creator><creator>Stanic, Aleksandar K</creator><creator>Brutkiewicz, Randy R</creator><creator>Medof, M. Edward</creator><creator>Joyce, Sebastian</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>20020115</creationdate><title>Lipid Protein Interactions: The Assembly of CD1d1 with Cellular Phospholipids Occurs in the Endoplasmic Reticulum</title><author>De Silva, A. Dharshan ; Park, J.-June ; Matsuki, Naoto ; Stanic, Aleksandar K ; Brutkiewicz, Randy R ; Medof, M. Edward ; Joyce, Sebastian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c405t-b6e2dc184469193e66b00c2236b3d2b893358081ede12de0fe5bc02517c9bf93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Animals</topic><topic>Antigen Presentation</topic><topic>Antigens, CD1 - metabolism</topic><topic>Antigens, CD1d</topic><topic>CD1d1 antigen</topic><topic>Dolichol Phosphates - metabolism</topic><topic>Endoplasmic Reticulum - enzymology</topic><topic>Endoplasmic Reticulum - immunology</topic><topic>Endoplasmic Reticulum - metabolism</topic><topic>Glycosylphosphatidylinositols - deficiency</topic><topic>Glycosylphosphatidylinositols - genetics</topic><topic>Glycosylphosphatidylinositols - metabolism</topic><topic>Humans</topic><topic>Intracellular Fluid - immunology</topic><topic>Intracellular Fluid - metabolism</topic><topic>K562 Cells</topic><topic>Ligands</topic><topic>Mannose - metabolism</topic><topic>Mice</topic><topic>Phosphatidylethanolamines - metabolism</topic><topic>phosphatidylinositol</topic><topic>Phosphatidylinositol Diacylglycerol-Lyase</topic><topic>Phosphatidylinositols - metabolism</topic><topic>Phospholipids - metabolism</topic><topic>Polysaccharides - metabolism</topic><topic>Tumor Cells, Cultured</topic><topic>Type C Phospholipases - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>De Silva, A. Dharshan</creatorcontrib><creatorcontrib>Park, J.-June</creatorcontrib><creatorcontrib>Matsuki, Naoto</creatorcontrib><creatorcontrib>Stanic, Aleksandar K</creatorcontrib><creatorcontrib>Brutkiewicz, Randy R</creatorcontrib><creatorcontrib>Medof, M. Edward</creatorcontrib><creatorcontrib>Joyce, Sebastian</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>De Silva, A. Dharshan</au><au>Park, J.-June</au><au>Matsuki, Naoto</au><au>Stanic, Aleksandar K</au><au>Brutkiewicz, Randy R</au><au>Medof, M. Edward</au><au>Joyce, Sebastian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lipid Protein Interactions: The Assembly of CD1d1 with Cellular Phospholipids Occurs in the Endoplasmic Reticulum</atitle><jtitle>The Journal of immunology (1950)</jtitle><addtitle>J Immunol</addtitle><date>2002-01-15</date><risdate>2002</risdate><volume>168</volume><issue>2</issue><spage>723</spage><epage>733</epage><pages>723-733</pages><issn>0022-1767</issn><eissn>1550-6606</eissn><abstract>CD1d1 is a member of a family of lipid Ag-presenting molecules. The cellular ligands associated with CD1d1 were isolated and characterized by biochemical means as an approach to elucidate the mechanism by which CD1 molecules assemble in vivo. Natural ligands of mouse CD1d1 included cellular phosphatidylinositol and phosphatidylinositol-glycans that are synthesized in the endoplasmic reticulum. Further biochemical data revealed that the two CD1d1 mutants, one defective in recycling from-and-to the plasma membrane and the other in efficiently negotiating the secretory pathway, associated with phosphatidylinositol. Thus phosphatidylinositol associated with CD1d1 in the early secretory pathway. Phosphatidylinositol also associated with CD1d1 in Pig-A-deficient cells that are defective in the first glycosylation step of glycosylphosphatidylinositol biosynthesis. Moreover, cellular phosphatidylinositol-glycans are not Valpha14Jalpha15 natural T cell Ags. Therefore, we predict that cellular lipids occlude the hydrophobic Ag-binding groove of CD1 during assembly until they are exchanged for a glycolipid Ag(s) within the recycling compartment for display on the plasma membrane. In this manner, cellular lipids might play a chaperone-like role in the assembly of CD1d1 in vivo, akin to the function of invariant chain in MHC class II assembly.</abstract><cop>United States</cop><pub>Am Assoc Immnol</pub><pmid>11777966</pmid><doi>10.4049/jimmunol.168.2.723</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antigen Presentation Antigens, CD1 - metabolism Antigens, CD1d CD1d1 antigen Dolichol Phosphates - metabolism Endoplasmic Reticulum - enzymology Endoplasmic Reticulum - immunology Endoplasmic Reticulum - metabolism Glycosylphosphatidylinositols - deficiency Glycosylphosphatidylinositols - genetics Glycosylphosphatidylinositols - metabolism Humans Intracellular Fluid - immunology Intracellular Fluid - metabolism K562 Cells Ligands Mannose - metabolism Mice Phosphatidylethanolamines - metabolism phosphatidylinositol Phosphatidylinositol Diacylglycerol-Lyase Phosphatidylinositols - metabolism Phospholipids - metabolism Polysaccharides - metabolism Tumor Cells, Cultured Type C Phospholipases - metabolism |
title | Lipid Protein Interactions: The Assembly of CD1d1 with Cellular Phospholipids Occurs in the Endoplasmic Reticulum |
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