Endogenous MHC-related protein 1 is transiently expressed on the plasma membrane in a conformation that activates mucosal-associated invariant T cells
The development of mucosal-associated invariant T (MAIT) cells is dependent upon the class Ib molecule MHC-related protein 1 (MR1), commensal bacteria, and a thymus. Furthermore, recent studies have implicated MR1 presentation to MAIT cells in bacteria recognition, although the mechanism remains und...
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Veröffentlicht in: | The Journal of immunology (1950) 2011-04, Vol.186 (8), p.4744-4750 |
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creator | Chua, Wei-Jen Kim, Sojung Myers, Nancy Huang, Shouxiong Yu, Lawrence Fremont, Daved H Diamond, Michael S Hansen, Ted H |
description | The development of mucosal-associated invariant T (MAIT) cells is dependent upon the class Ib molecule MHC-related protein 1 (MR1), commensal bacteria, and a thymus. Furthermore, recent studies have implicated MR1 presentation to MAIT cells in bacteria recognition, although the mechanism remains undefined. Surprisingly, however, surface expression of MR1 has been difficult to detect serologically, despite ubiquitous detection of MR1 transcripts and intracellular protein. In this article, we define a unique mAb capable of stabilizing endogenous mouse MR1 at the cell surface, resulting in enhanced mouse MAIT cell activation. Our results demonstrated that under basal conditions, endogenous MR1 transiently visits the cell surface, thus reconciling the aforementioned serologic and functional studies. Furthermore, using this approach, double-positive thymocytes, macrophages, and dendritic cells were identified as potential APCs for MAIT cell development and activation. Based on this pattern of MR1 expression, it is intriguing to speculate that constitutive expression of MR1 may be detrimental for maintenance of immune homeostasis in the gut and/or detection of pathogenic bacteria in mucosal tissues. |
doi_str_mv | 10.4049/jimmunol.1003254 |
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Furthermore, recent studies have implicated MR1 presentation to MAIT cells in bacteria recognition, although the mechanism remains undefined. Surprisingly, however, surface expression of MR1 has been difficult to detect serologically, despite ubiquitous detection of MR1 transcripts and intracellular protein. In this article, we define a unique mAb capable of stabilizing endogenous mouse MR1 at the cell surface, resulting in enhanced mouse MAIT cell activation. Our results demonstrated that under basal conditions, endogenous MR1 transiently visits the cell surface, thus reconciling the aforementioned serologic and functional studies. Furthermore, using this approach, double-positive thymocytes, macrophages, and dendritic cells were identified as potential APCs for MAIT cell development and activation. Based on this pattern of MR1 expression, it is intriguing to speculate that constitutive expression of MR1 may be detrimental for maintenance of immune homeostasis in the gut and/or detection of pathogenic bacteria in mucosal tissues.</description><identifier>ISSN: 0022-1767</identifier><identifier>EISSN: 1550-6606</identifier><identifier>DOI: 10.4049/jimmunol.1003254</identifier><identifier>PMID: 21402896</identifier><language>eng</language><publisher>United States</publisher><subject>Animals ; Antibodies, Monoclonal - immunology ; Antibodies, Monoclonal - metabolism ; B-Lymphocytes - immunology ; B-Lymphocytes - metabolism ; Cattle ; Cell Membrane - immunology ; Cell Membrane - metabolism ; Cross Reactions - immunology ; Dendritic Cells - immunology ; Dendritic Cells - metabolism ; Epitopes - immunology ; Epitopes - metabolism ; Flow Cytometry ; Histocompatibility Antigens Class I - genetics ; Histocompatibility Antigens Class I - immunology ; Histocompatibility Antigens Class I - metabolism ; Humans ; Hybridomas - immunology ; Lymphocyte Activation - immunology ; Macrophages - immunology ; Macrophages - metabolism ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Minor Histocompatibility Antigens ; Mucous Membrane - cytology ; Mucous Membrane - immunology ; Mucous Membrane - metabolism ; Protein Binding ; Rats ; T-Lymphocytes - immunology ; T-Lymphocytes - metabolism ; Thymus Gland - cytology ; Thymus Gland - immunology ; Thymus Gland - metabolism</subject><ispartof>The Journal of immunology (1950), 2011-04, Vol.186 (8), p.4744-4750</ispartof><rights>Copyright © 2011 by The American Association of Immunologists, Inc. 2011</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c427t-ac0bace7020281d120910b2f93d5176d6b079bb5d3df94bbedef1b1c1abc12a83</citedby><cites>FETCH-LOGICAL-c427t-ac0bace7020281d120910b2f93d5176d6b079bb5d3df94bbedef1b1c1abc12a83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,777,781,882,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21402896$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chua, Wei-Jen</creatorcontrib><creatorcontrib>Kim, Sojung</creatorcontrib><creatorcontrib>Myers, Nancy</creatorcontrib><creatorcontrib>Huang, Shouxiong</creatorcontrib><creatorcontrib>Yu, Lawrence</creatorcontrib><creatorcontrib>Fremont, Daved H</creatorcontrib><creatorcontrib>Diamond, Michael S</creatorcontrib><creatorcontrib>Hansen, Ted H</creatorcontrib><title>Endogenous MHC-related protein 1 is transiently expressed on the plasma membrane in a conformation that activates mucosal-associated invariant T cells</title><title>The Journal of immunology (1950)</title><addtitle>J Immunol</addtitle><description>The development of mucosal-associated invariant T (MAIT) cells is dependent upon the class Ib molecule MHC-related protein 1 (MR1), commensal bacteria, and a thymus. 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Based on this pattern of MR1 expression, it is intriguing to speculate that constitutive expression of MR1 may be detrimental for maintenance of immune homeostasis in the gut and/or detection of pathogenic bacteria in mucosal tissues.</description><subject>Animals</subject><subject>Antibodies, Monoclonal - immunology</subject><subject>Antibodies, Monoclonal - metabolism</subject><subject>B-Lymphocytes - immunology</subject><subject>B-Lymphocytes - metabolism</subject><subject>Cattle</subject><subject>Cell Membrane - immunology</subject><subject>Cell Membrane - metabolism</subject><subject>Cross Reactions - immunology</subject><subject>Dendritic Cells - immunology</subject><subject>Dendritic Cells - metabolism</subject><subject>Epitopes - immunology</subject><subject>Epitopes - metabolism</subject><subject>Flow Cytometry</subject><subject>Histocompatibility Antigens Class I - genetics</subject><subject>Histocompatibility Antigens Class I - immunology</subject><subject>Histocompatibility Antigens Class I - metabolism</subject><subject>Humans</subject><subject>Hybridomas - immunology</subject><subject>Lymphocyte Activation - immunology</subject><subject>Macrophages - immunology</subject><subject>Macrophages - metabolism</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Knockout</subject><subject>Minor Histocompatibility Antigens</subject><subject>Mucous Membrane - cytology</subject><subject>Mucous Membrane - immunology</subject><subject>Mucous Membrane - metabolism</subject><subject>Protein Binding</subject><subject>Rats</subject><subject>T-Lymphocytes - immunology</subject><subject>T-Lymphocytes - metabolism</subject><subject>Thymus Gland - cytology</subject><subject>Thymus Gland - immunology</subject><subject>Thymus Gland - metabolism</subject><issn>0022-1767</issn><issn>1550-6606</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkTFvFDEQhS0EIkegp0LuqDaMvbv2bYOEToFECqIJtTX2ehNHa3uxvSfyR_i9OMklChWVi_neG795hLxncNJBN3y6cd6vIc4nDKDlffeCbFjfQyMEiJdkA8B5w6SQR-RNzjcAIIB3r8kRZx3w7SA25M9pGOOVDXHN9PvZrkl2xmJHuqRYrAuUUZdpSRiys6HMt9T-XpLNuSIx0HJt6TJj9ki99bpillYRUhPDFJPH4u4pLBRNcftqnalfTcw4N5hzNO5-mwt7TA5DoZfU2HnOb8mrCeds3x3eY_Lz6-nl7qy5-PHtfPflojEdl6VBAxqNlcBrHDYyDgMDzaehHfuaexQa5KB1P7bjNHRa29FOTDPDUBvGcdsek88PvsuqvR1NzZhwVktyHtOtiujUv5PgrtVV3KtWsK2QUA0-HgxS_LXaXJR3-S5CPUW9qRqg6yRjUv6X3ApoBzkAqyQ8kCbFnJOdnv7DQN31rh57V4feq-TD8xxPgsei279vA7BS</recordid><startdate>20110415</startdate><enddate>20110415</enddate><creator>Chua, Wei-Jen</creator><creator>Kim, Sojung</creator><creator>Myers, Nancy</creator><creator>Huang, Shouxiong</creator><creator>Yu, Lawrence</creator><creator>Fremont, Daved H</creator><creator>Diamond, Michael S</creator><creator>Hansen, Ted H</creator><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><scope>7T5</scope><scope>H94</scope><scope>5PM</scope></search><sort><creationdate>20110415</creationdate><title>Endogenous MHC-related protein 1 is transiently expressed on the plasma membrane in a conformation that activates mucosal-associated invariant T cells</title><author>Chua, Wei-Jen ; Kim, Sojung ; Myers, Nancy ; Huang, Shouxiong ; Yu, Lawrence ; Fremont, Daved H ; Diamond, Michael S ; Hansen, Ted H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c427t-ac0bace7020281d120910b2f93d5176d6b079bb5d3df94bbedef1b1c1abc12a83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Animals</topic><topic>Antibodies, Monoclonal - immunology</topic><topic>Antibodies, Monoclonal - metabolism</topic><topic>B-Lymphocytes - immunology</topic><topic>B-Lymphocytes - metabolism</topic><topic>Cattle</topic><topic>Cell Membrane - immunology</topic><topic>Cell Membrane - metabolism</topic><topic>Cross Reactions - immunology</topic><topic>Dendritic Cells - immunology</topic><topic>Dendritic Cells - metabolism</topic><topic>Epitopes - immunology</topic><topic>Epitopes - metabolism</topic><topic>Flow Cytometry</topic><topic>Histocompatibility Antigens Class I - genetics</topic><topic>Histocompatibility Antigens Class I - immunology</topic><topic>Histocompatibility Antigens Class I - metabolism</topic><topic>Humans</topic><topic>Hybridomas - immunology</topic><topic>Lymphocyte Activation - immunology</topic><topic>Macrophages - immunology</topic><topic>Macrophages - metabolism</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Knockout</topic><topic>Minor Histocompatibility Antigens</topic><topic>Mucous Membrane - cytology</topic><topic>Mucous Membrane - immunology</topic><topic>Mucous Membrane - metabolism</topic><topic>Protein Binding</topic><topic>Rats</topic><topic>T-Lymphocytes - immunology</topic><topic>T-Lymphocytes - metabolism</topic><topic>Thymus Gland - cytology</topic><topic>Thymus Gland - immunology</topic><topic>Thymus Gland - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chua, Wei-Jen</creatorcontrib><creatorcontrib>Kim, Sojung</creatorcontrib><creatorcontrib>Myers, Nancy</creatorcontrib><creatorcontrib>Huang, Shouxiong</creatorcontrib><creatorcontrib>Yu, Lawrence</creatorcontrib><creatorcontrib>Fremont, Daved H</creatorcontrib><creatorcontrib>Diamond, Michael S</creatorcontrib><creatorcontrib>Hansen, Ted 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><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of immunology (1950)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chua, Wei-Jen</au><au>Kim, Sojung</au><au>Myers, Nancy</au><au>Huang, Shouxiong</au><au>Yu, Lawrence</au><au>Fremont, Daved H</au><au>Diamond, Michael S</au><au>Hansen, Ted H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Endogenous MHC-related protein 1 is transiently expressed on the plasma membrane in a conformation that activates mucosal-associated invariant T cells</atitle><jtitle>The Journal of immunology (1950)</jtitle><addtitle>J Immunol</addtitle><date>2011-04-15</date><risdate>2011</risdate><volume>186</volume><issue>8</issue><spage>4744</spage><epage>4750</epage><pages>4744-4750</pages><issn>0022-1767</issn><eissn>1550-6606</eissn><abstract>The development of mucosal-associated invariant T (MAIT) cells is dependent upon the class Ib molecule MHC-related protein 1 (MR1), commensal bacteria, and a thymus. Furthermore, recent studies have implicated MR1 presentation to MAIT cells in bacteria recognition, although the mechanism remains undefined. Surprisingly, however, surface expression of MR1 has been difficult to detect serologically, despite ubiquitous detection of MR1 transcripts and intracellular protein. In this article, we define a unique mAb capable of stabilizing endogenous mouse MR1 at the cell surface, resulting in enhanced mouse MAIT cell activation. Our results demonstrated that under basal conditions, endogenous MR1 transiently visits the cell surface, thus reconciling the aforementioned serologic and functional studies. Furthermore, using this approach, double-positive thymocytes, macrophages, and dendritic cells were identified as potential APCs for MAIT cell development and activation. 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subjects | Animals Antibodies, Monoclonal - immunology Antibodies, Monoclonal - metabolism B-Lymphocytes - immunology B-Lymphocytes - metabolism Cattle Cell Membrane - immunology Cell Membrane - metabolism Cross Reactions - immunology Dendritic Cells - immunology Dendritic Cells - metabolism Epitopes - immunology Epitopes - metabolism Flow Cytometry Histocompatibility Antigens Class I - genetics Histocompatibility Antigens Class I - immunology Histocompatibility Antigens Class I - metabolism Humans Hybridomas - immunology Lymphocyte Activation - immunology Macrophages - immunology Macrophages - metabolism Mice Mice, Inbred C57BL Mice, Knockout Minor Histocompatibility Antigens Mucous Membrane - cytology Mucous Membrane - immunology Mucous Membrane - metabolism Protein Binding Rats T-Lymphocytes - immunology T-Lymphocytes - metabolism Thymus Gland - cytology Thymus Gland - immunology Thymus Gland - metabolism |
title | Endogenous MHC-related protein 1 is transiently expressed on the plasma membrane in a conformation that activates mucosal-associated invariant T cells |
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