Loading…

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...

Full description

Saved in:
Bibliographic Details
Published in:The Journal of immunology (1950) 2002-01, Vol.168 (2), p.723-733
Main Authors: De Silva, A. Dharshan, Park, J.-June, Matsuki, Naoto, Stanic, Aleksandar K, Brutkiewicz, Randy R, Medof, M. Edward, Joyce, Sebastian
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c405t-b6e2dc184469193e66b00c2236b3d2b893358081ede12de0fe5bc02517c9bf93
cites cdi_FETCH-LOGICAL-c405t-b6e2dc184469193e66b00c2236b3d2b893358081ede12de0fe5bc02517c9bf93
container_end_page 733
container_issue 2
container_start_page 723
container_title The Journal of immunology (1950)
container_volume 168
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
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_71355073</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>18239229</sourcerecordid><originalsourceid>FETCH-LOGICAL-c405t-b6e2dc184469193e66b00c2236b3d2b893358081ede12de0fe5bc02517c9bf93</originalsourceid><addsrcrecordid>eNqFkcFq3DAQhkVoSLZpX6CHolNv3mokW7J7C5u0DSwkhL0LWx7XCpLlSDYmb18v2bLHnuby_98M8xHyBdg2Z3n1_cV6Pw_BbUGWW75VXFyQDRQFy6Rk8gPZMMZ5Bkqqa_IxpRfGmGQ8vyLXAEqpSsoNed3b0bb0KYYJ7UAfhgljbSYbhvSDHnqktymhb9wbDR3d3UELdLFTT3fo3OzqSJ_6kMY-uCMm0Udj5pjoSprW7v3QhtHVyVtDn3GyZnaz_0Quu9ol_HyaN-Tw8_6w-53tH3897G73mclZMWWNRN4aKPNcVlAJlLJhzHAuZCNa3pSVEEXJSsAWgbfIOiwaw3gBylRNV4kb8u0dO8bwOmOatLfJrFfXA4Y5aQVi_ZQS_w1CyUXF-ZHI34MmhpQidnqM1tfxTQPTRyH6nxC9CtFcr0LW0tcTfW48tufKycB5fW__9IuNqJOvnVvjoJdlOZP-Agmolsk</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>18239229</pqid></control><display><type>article</type><title>Lipid Protein Interactions: The Assembly of CD1d1 with Cellular Phospholipids Occurs in the Endoplasmic Reticulum</title><source>Electronic Journals Library</source><creator>De Silva, A. 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>
fulltext fulltext
identifier ISSN: 0022-1767
ispartof The Journal of immunology (1950), 2002-01, Vol.168 (2), p.723-733
issn 0022-1767
1550-6606
language eng
recordid cdi_proquest_miscellaneous_71355073
source Electronic Journals Library
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
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-28T06%3A00%3A17IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Lipid%20Protein%20Interactions:%20The%20Assembly%20of%20CD1d1%20with%20Cellular%20Phospholipids%20Occurs%20in%20the%20Endoplasmic%20Reticulum&rft.jtitle=The%20Journal%20of%20immunology%20(1950)&rft.au=De%20Silva,%20A.%20Dharshan&rft.date=2002-01-15&rft.volume=168&rft.issue=2&rft.spage=723&rft.epage=733&rft.pages=723-733&rft.issn=0022-1767&rft.eissn=1550-6606&rft_id=info:doi/10.4049/jimmunol.168.2.723&rft_dat=%3Cproquest_cross%3E18239229%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c405t-b6e2dc184469193e66b00c2236b3d2b893358081ede12de0fe5bc02517c9bf93%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=18239229&rft_id=info:pmid/11777966&rfr_iscdi=true