Polymeric immunoglobulin receptor
The surface of mucosal sites, such as the intestinal tract, are covered by epithelial cells. To protect the intestinal environment from invading pathogens and maintain homeostasis, the human body developed an exquisite acquired immune system, referred to as the mucosal immune system, in which epithe...
Gespeichert in:
Veröffentlicht in: | Journal of Oral Science 2011, Vol.53(2), pp.147-156 |
---|---|
Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 156 |
---|---|
container_issue | 2 |
container_start_page | 147 |
container_title | Journal of Oral Science |
container_volume | 53 |
creator | Asano, Masatake Komiyama, Kazuo |
description | The surface of mucosal sites, such as the intestinal tract, are covered by epithelial cells. To protect the intestinal environment from invading pathogens and maintain homeostasis, the human body developed an exquisite acquired immune system, referred to as the mucosal immune system, in which epithelial cells and lymphocytes function cooperatively. The main player in this immune system is the polymeric immunoglobulins (pIgs), in particular dimeric IgA (dIgA). To exert its protective effect, dIgA produced in the lamina propria must be transported to the intestinal lumen across epithelial cells. This process is called transcytosis and is mediated by polymeric immunoglobulin receptor (pIgR), which is exclusively produced by intestinal epithelial cells (IECs). DIgA is captured by pIgR on the basolateral surface of IECs and transcytosed to the opposite side of IECs. The dIgA-pIgR complex is expressed on the apical surface of IECs and proteolytically cleaved to generate secretory IgA (SIgA). This review describes the current understanding and recent progress in this research field. (J Oral Sci 53, 147-156, 2011) |
doi_str_mv | 10.2334/josnusd.53.147 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_874296621</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>874296621</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5007-bc79ed85ca244eb3a20bb4cd5c7b564d9788d8711634bb3459fc43af097a5c503</originalsourceid><addsrcrecordid>eNpNkDtPwzAURi0EoqWwMqIyMSX4bWdEFS-pEgwwW7bjlFROXOxk6L_HKKViufeT7rln-AC4RrDEhND7bUj9mOqSkRJRcQLmSEpY0Arz05wJJTkTOgMXKW0hpJgLdg5mGAmEOZJzcPse_L5zsbXLtuvGPmx8MKNv-2V01u2GEC_BWaN9cleHvQCfT48fq5di_fb8unpYF5ZBKApjReVqyazGlDpDNIbGUFszKwzjtK6ElLUUCHFCjSGUVY2lRDewEpplBVmAu8m7i-F7dGlQXZus8173LoxJSUFxxTlGmSwn0saQUnSN2sW203GvEFS_rahDK4oRlVvJDzcH9Wg6Vx_xvxoysJqAbRr0xh0BHYfWevffh6eRtcer_dJRuZ78AIz2dz8</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>874296621</pqid></control><display><type>article</type><title>Polymeric immunoglobulin receptor</title><source>MEDLINE</source><source>J-STAGE (Japan Science & Technology Information Aggregator, Electronic) Freely Available Titles - Japanese</source><source>Open Access Titles of Japan</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><creator>Asano, Masatake ; Komiyama, Kazuo</creator><creatorcontrib>Asano, Masatake ; Komiyama, Kazuo</creatorcontrib><description>The surface of mucosal sites, such as the intestinal tract, are covered by epithelial cells. To protect the intestinal environment from invading pathogens and maintain homeostasis, the human body developed an exquisite acquired immune system, referred to as the mucosal immune system, in which epithelial cells and lymphocytes function cooperatively. The main player in this immune system is the polymeric immunoglobulins (pIgs), in particular dimeric IgA (dIgA). To exert its protective effect, dIgA produced in the lamina propria must be transported to the intestinal lumen across epithelial cells. This process is called transcytosis and is mediated by polymeric immunoglobulin receptor (pIgR), which is exclusively produced by intestinal epithelial cells (IECs). DIgA is captured by pIgR on the basolateral surface of IECs and transcytosed to the opposite side of IECs. The dIgA-pIgR complex is expressed on the apical surface of IECs and proteolytically cleaved to generate secretory IgA (SIgA). This review describes the current understanding and recent progress in this research field. (J Oral Sci 53, 147-156, 2011)</description><identifier>ISSN: 1343-4934</identifier><identifier>EISSN: 1880-4926</identifier><identifier>DOI: 10.2334/josnusd.53.147</identifier><identifier>PMID: 21712618</identifier><language>eng</language><publisher>Japan: Nihon University School of Dentistry</publisher><subject>Biopolymers - immunology ; Dentistry ; dimeric IgA ; Epithelial Cells - immunology ; Humans ; Immunoglobulin A - immunology ; Immunoglobulin A, Secretory - immunology ; intestinal epithelial cells ; Intestinal Mucosa - immunology ; polymeric immunoglobulin receptor ; Receptors, Polymeric Immunoglobulin - genetics ; Receptors, Polymeric Immunoglobulin - immunology ; Transcription, Genetic - genetics ; transcytosis ; Transcytosis - immunology</subject><ispartof>Journal of Oral Science, 2011, Vol.53(2), pp.147-156</ispartof><rights>2011 by Nihon University School of Dentistry</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5007-bc79ed85ca244eb3a20bb4cd5c7b564d9788d8711634bb3459fc43af097a5c503</citedby><cites>FETCH-LOGICAL-c5007-bc79ed85ca244eb3a20bb4cd5c7b564d9788d8711634bb3459fc43af097a5c503</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1877,4010,27900,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21712618$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Asano, Masatake</creatorcontrib><creatorcontrib>Komiyama, Kazuo</creatorcontrib><title>Polymeric immunoglobulin receptor</title><title>Journal of Oral Science</title><addtitle>J Oral Sci</addtitle><description>The surface of mucosal sites, such as the intestinal tract, are covered by epithelial cells. To protect the intestinal environment from invading pathogens and maintain homeostasis, the human body developed an exquisite acquired immune system, referred to as the mucosal immune system, in which epithelial cells and lymphocytes function cooperatively. The main player in this immune system is the polymeric immunoglobulins (pIgs), in particular dimeric IgA (dIgA). To exert its protective effect, dIgA produced in the lamina propria must be transported to the intestinal lumen across epithelial cells. This process is called transcytosis and is mediated by polymeric immunoglobulin receptor (pIgR), which is exclusively produced by intestinal epithelial cells (IECs). DIgA is captured by pIgR on the basolateral surface of IECs and transcytosed to the opposite side of IECs. The dIgA-pIgR complex is expressed on the apical surface of IECs and proteolytically cleaved to generate secretory IgA (SIgA). This review describes the current understanding and recent progress in this research field. (J Oral Sci 53, 147-156, 2011)</description><subject>Biopolymers - immunology</subject><subject>Dentistry</subject><subject>dimeric IgA</subject><subject>Epithelial Cells - immunology</subject><subject>Humans</subject><subject>Immunoglobulin A - immunology</subject><subject>Immunoglobulin A, Secretory - immunology</subject><subject>intestinal epithelial cells</subject><subject>Intestinal Mucosa - immunology</subject><subject>polymeric immunoglobulin receptor</subject><subject>Receptors, Polymeric Immunoglobulin - genetics</subject><subject>Receptors, Polymeric Immunoglobulin - immunology</subject><subject>Transcription, Genetic - genetics</subject><subject>transcytosis</subject><subject>Transcytosis - immunology</subject><issn>1343-4934</issn><issn>1880-4926</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkDtPwzAURi0EoqWwMqIyMSX4bWdEFS-pEgwwW7bjlFROXOxk6L_HKKViufeT7rln-AC4RrDEhND7bUj9mOqSkRJRcQLmSEpY0Arz05wJJTkTOgMXKW0hpJgLdg5mGAmEOZJzcPse_L5zsbXLtuvGPmx8MKNv-2V01u2GEC_BWaN9cleHvQCfT48fq5di_fb8unpYF5ZBKApjReVqyazGlDpDNIbGUFszKwzjtK6ElLUUCHFCjSGUVY2lRDewEpplBVmAu8m7i-F7dGlQXZus8173LoxJSUFxxTlGmSwn0saQUnSN2sW203GvEFS_rahDK4oRlVvJDzcH9Wg6Vx_xvxoysJqAbRr0xh0BHYfWevffh6eRtcer_dJRuZ78AIz2dz8</recordid><startdate>2011</startdate><enddate>2011</enddate><creator>Asano, Masatake</creator><creator>Komiyama, Kazuo</creator><general>Nihon University School of Dentistry</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>2011</creationdate><title>Polymeric immunoglobulin receptor</title><author>Asano, Masatake ; Komiyama, Kazuo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5007-bc79ed85ca244eb3a20bb4cd5c7b564d9788d8711634bb3459fc43af097a5c503</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Biopolymers - immunology</topic><topic>Dentistry</topic><topic>dimeric IgA</topic><topic>Epithelial Cells - immunology</topic><topic>Humans</topic><topic>Immunoglobulin A - immunology</topic><topic>Immunoglobulin A, Secretory - immunology</topic><topic>intestinal epithelial cells</topic><topic>Intestinal Mucosa - immunology</topic><topic>polymeric immunoglobulin receptor</topic><topic>Receptors, Polymeric Immunoglobulin - genetics</topic><topic>Receptors, Polymeric Immunoglobulin - immunology</topic><topic>Transcription, Genetic - genetics</topic><topic>transcytosis</topic><topic>Transcytosis - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Asano, Masatake</creatorcontrib><creatorcontrib>Komiyama, Kazuo</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 Oral Science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Asano, Masatake</au><au>Komiyama, Kazuo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Polymeric immunoglobulin receptor</atitle><jtitle>Journal of Oral Science</jtitle><addtitle>J Oral Sci</addtitle><date>2011</date><risdate>2011</risdate><volume>53</volume><issue>2</issue><spage>147</spage><epage>156</epage><pages>147-156</pages><issn>1343-4934</issn><eissn>1880-4926</eissn><abstract>The surface of mucosal sites, such as the intestinal tract, are covered by epithelial cells. To protect the intestinal environment from invading pathogens and maintain homeostasis, the human body developed an exquisite acquired immune system, referred to as the mucosal immune system, in which epithelial cells and lymphocytes function cooperatively. The main player in this immune system is the polymeric immunoglobulins (pIgs), in particular dimeric IgA (dIgA). To exert its protective effect, dIgA produced in the lamina propria must be transported to the intestinal lumen across epithelial cells. This process is called transcytosis and is mediated by polymeric immunoglobulin receptor (pIgR), which is exclusively produced by intestinal epithelial cells (IECs). DIgA is captured by pIgR on the basolateral surface of IECs and transcytosed to the opposite side of IECs. The dIgA-pIgR complex is expressed on the apical surface of IECs and proteolytically cleaved to generate secretory IgA (SIgA). This review describes the current understanding and recent progress in this research field. (J Oral Sci 53, 147-156, 2011)</abstract><cop>Japan</cop><pub>Nihon University School of Dentistry</pub><pmid>21712618</pmid><doi>10.2334/josnusd.53.147</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1343-4934 |
ispartof | Journal of Oral Science, 2011, Vol.53(2), pp.147-156 |
issn | 1343-4934 1880-4926 |
language | eng |
recordid | cdi_proquest_miscellaneous_874296621 |
source | MEDLINE; J-STAGE (Japan Science & Technology Information Aggregator, Electronic) Freely Available Titles - Japanese; Open Access Titles of Japan; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
subjects | Biopolymers - immunology Dentistry dimeric IgA Epithelial Cells - immunology Humans Immunoglobulin A - immunology Immunoglobulin A, Secretory - immunology intestinal epithelial cells Intestinal Mucosa - immunology polymeric immunoglobulin receptor Receptors, Polymeric Immunoglobulin - genetics Receptors, Polymeric Immunoglobulin - immunology Transcription, Genetic - genetics transcytosis Transcytosis - immunology |
title | Polymeric immunoglobulin receptor |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-13T10%3A59%3A38IST&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=Polymeric%20immunoglobulin%20receptor&rft.jtitle=Journal%20of%20Oral%20Science&rft.au=Asano,%20Masatake&rft.date=2011&rft.volume=53&rft.issue=2&rft.spage=147&rft.epage=156&rft.pages=147-156&rft.issn=1343-4934&rft.eissn=1880-4926&rft_id=info:doi/10.2334/josnusd.53.147&rft_dat=%3Cproquest_cross%3E874296621%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=874296621&rft_id=info:pmid/21712618&rfr_iscdi=true |