The TNF Family of Ligands and Receptors: Communication Modules in the Immune System and Beyond

The tumor necrosis factor (TNF) and TNF receptor (TNFR) superfamilies (TNFSF/TNFRSF) include 19 ligands and 29 receptors that play important roles in the modulation of cellular functions. The communication pathways mediated by TNFSF/TNFRSF are essential for numerous developmental, homeostatic, and s...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Physiological reviews 2019-01, Vol.99 (1), p.115-160
Hauptverfasser: Dostert, Catherine, Grusdat, Melanie, Letellier, Elisabeth, Brenner, Dirk
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 160
container_issue 1
container_start_page 115
container_title Physiological reviews
container_volume 99
creator Dostert, Catherine
Grusdat, Melanie
Letellier, Elisabeth
Brenner, Dirk
description The tumor necrosis factor (TNF) and TNF receptor (TNFR) superfamilies (TNFSF/TNFRSF) include 19 ligands and 29 receptors that play important roles in the modulation of cellular functions. The communication pathways mediated by TNFSF/TNFRSF are essential for numerous developmental, homeostatic, and stimulus-responsive processes in vivo. TNFSF/TNFRSF members regulate cellular differentiation, survival, and programmed death, but their most critical functions pertain to the immune system. Both innate and adaptive immune cells are controlled by TNFSF/TNFRSF members in a manner that is crucial for the coordination of various mechanisms driving either co-stimulation or co-inhibition of the immune response. Dysregulation of these same signaling pathways has been implicated in inflammatory and autoimmune diseases, highlighting the importance of their tight regulation. Investigation of the control of TNFSF/TNFRSF activities has led to the development of therapeutics with the potential to reduce chronic inflammation or promote anti-tumor immunity. The study of TNFSF/TNFRSF proteins has exploded over the last 30 yr, but there remains a need to better understand the fundamental mechanisms underlying the molecular pathways they mediate to design more effective anti-inflammatory and anti-cancer therapies.
doi_str_mv 10.1152/physrev.00045.2017
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2125308764</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2125308764</sourcerecordid><originalsourceid>FETCH-LOGICAL-c490t-88e8ff5e427198f27cf80274983806595799f36ccb8770a3435f746600edfe703</originalsourceid><addsrcrecordid>eNpdkD1PwzAQhi0EglL4AwzIEgtLyvkrdtigooBUQIKyEoXkDEFJXOIEKf8elxYGlvNwz_ue9RByxGDCmOJny_fBt_g1AQCpJhyY3iKjsOAR4wy2yQhAsCgRQuyRfe8_AqdUrHbJngChZBLLEXlZvCNd3M_oLKvLaqDO0nn5ljWFp2HQR8xx2bnWn9Opq-u-KfOsK11D71zRV-hp2dAuNNyudkifBt9h_ZO8xME1xQHZsVnl8XDzjsnz7GoxvYnmD9e304t5lMsEusgYNNYqlFyzxFiuc2uAa5kYYSBWidJJYkWc569Ga8iEFMpqGccAWFjUIMbkdN27bN1nj75L69LnWFVZg673KWdcCTA6lgE9-Yd-uL5twu8CZSQHYcLZMeFrKm-dD5ZtumzLOmuHlEG6sp9u7Kc_9tOV_RA63lT3rzUWf5Ff3eIbL0d_gA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2184203898</pqid></control><display><type>article</type><title>The TNF Family of Ligands and Receptors: Communication Modules in the Immune System and Beyond</title><source>American Physiological Society</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Alma/SFX Local Collection</source><creator>Dostert, Catherine ; Grusdat, Melanie ; Letellier, Elisabeth ; Brenner, Dirk</creator><creatorcontrib>Dostert, Catherine ; Grusdat, Melanie ; Letellier, Elisabeth ; Brenner, Dirk</creatorcontrib><description>The tumor necrosis factor (TNF) and TNF receptor (TNFR) superfamilies (TNFSF/TNFRSF) include 19 ligands and 29 receptors that play important roles in the modulation of cellular functions. The communication pathways mediated by TNFSF/TNFRSF are essential for numerous developmental, homeostatic, and stimulus-responsive processes in vivo. TNFSF/TNFRSF members regulate cellular differentiation, survival, and programmed death, but their most critical functions pertain to the immune system. Both innate and adaptive immune cells are controlled by TNFSF/TNFRSF members in a manner that is crucial for the coordination of various mechanisms driving either co-stimulation or co-inhibition of the immune response. Dysregulation of these same signaling pathways has been implicated in inflammatory and autoimmune diseases, highlighting the importance of their tight regulation. Investigation of the control of TNFSF/TNFRSF activities has led to the development of therapeutics with the potential to reduce chronic inflammation or promote anti-tumor immunity. The study of TNFSF/TNFRSF proteins has exploded over the last 30 yr, but there remains a need to better understand the fundamental mechanisms underlying the molecular pathways they mediate to design more effective anti-inflammatory and anti-cancer therapies.</description><identifier>ISSN: 0031-9333</identifier><identifier>EISSN: 1522-1210</identifier><identifier>DOI: 10.1152/physrev.00045.2017</identifier><identifier>PMID: 30354964</identifier><language>eng</language><publisher>United States: American Physiological Society</publisher><subject>Apoptosis ; Autoimmune diseases ; Cancer ; Drug development ; Immune response ; Immune system ; Ligands ; Tumor necrosis factor ; Tumor necrosis factor receptors ; Tumor necrosis factor-TNF</subject><ispartof>Physiological reviews, 2019-01, Vol.99 (1), p.115-160</ispartof><rights>Copyright American Physiological Society Jan 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c490t-88e8ff5e427198f27cf80274983806595799f36ccb8770a3435f746600edfe703</citedby><cites>FETCH-LOGICAL-c490t-88e8ff5e427198f27cf80274983806595799f36ccb8770a3435f746600edfe703</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3026,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30354964$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dostert, Catherine</creatorcontrib><creatorcontrib>Grusdat, Melanie</creatorcontrib><creatorcontrib>Letellier, Elisabeth</creatorcontrib><creatorcontrib>Brenner, Dirk</creatorcontrib><title>The TNF Family of Ligands and Receptors: Communication Modules in the Immune System and Beyond</title><title>Physiological reviews</title><addtitle>Physiol Rev</addtitle><description>The tumor necrosis factor (TNF) and TNF receptor (TNFR) superfamilies (TNFSF/TNFRSF) include 19 ligands and 29 receptors that play important roles in the modulation of cellular functions. The communication pathways mediated by TNFSF/TNFRSF are essential for numerous developmental, homeostatic, and stimulus-responsive processes in vivo. TNFSF/TNFRSF members regulate cellular differentiation, survival, and programmed death, but their most critical functions pertain to the immune system. Both innate and adaptive immune cells are controlled by TNFSF/TNFRSF members in a manner that is crucial for the coordination of various mechanisms driving either co-stimulation or co-inhibition of the immune response. Dysregulation of these same signaling pathways has been implicated in inflammatory and autoimmune diseases, highlighting the importance of their tight regulation. Investigation of the control of TNFSF/TNFRSF activities has led to the development of therapeutics with the potential to reduce chronic inflammation or promote anti-tumor immunity. The study of TNFSF/TNFRSF proteins has exploded over the last 30 yr, but there remains a need to better understand the fundamental mechanisms underlying the molecular pathways they mediate to design more effective anti-inflammatory and anti-cancer therapies.</description><subject>Apoptosis</subject><subject>Autoimmune diseases</subject><subject>Cancer</subject><subject>Drug development</subject><subject>Immune response</subject><subject>Immune system</subject><subject>Ligands</subject><subject>Tumor necrosis factor</subject><subject>Tumor necrosis factor receptors</subject><subject>Tumor necrosis factor-TNF</subject><issn>0031-9333</issn><issn>1522-1210</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNpdkD1PwzAQhi0EglL4AwzIEgtLyvkrdtigooBUQIKyEoXkDEFJXOIEKf8elxYGlvNwz_ue9RByxGDCmOJny_fBt_g1AQCpJhyY3iKjsOAR4wy2yQhAsCgRQuyRfe8_AqdUrHbJngChZBLLEXlZvCNd3M_oLKvLaqDO0nn5ljWFp2HQR8xx2bnWn9Opq-u-KfOsK11D71zRV-hp2dAuNNyudkifBt9h_ZO8xME1xQHZsVnl8XDzjsnz7GoxvYnmD9e304t5lMsEusgYNNYqlFyzxFiuc2uAa5kYYSBWidJJYkWc569Ga8iEFMpqGccAWFjUIMbkdN27bN1nj75L69LnWFVZg673KWdcCTA6lgE9-Yd-uL5twu8CZSQHYcLZMeFrKm-dD5ZtumzLOmuHlEG6sp9u7Kc_9tOV_RA63lT3rzUWf5Ff3eIbL0d_gA</recordid><startdate>20190101</startdate><enddate>20190101</enddate><creator>Dostert, Catherine</creator><creator>Grusdat, Melanie</creator><creator>Letellier, Elisabeth</creator><creator>Brenner, Dirk</creator><general>American Physiological Society</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7TK</scope><scope>7TS</scope><scope>7X8</scope></search><sort><creationdate>20190101</creationdate><title>The TNF Family of Ligands and Receptors: Communication Modules in the Immune System and Beyond</title><author>Dostert, Catherine ; Grusdat, Melanie ; Letellier, Elisabeth ; Brenner, Dirk</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c490t-88e8ff5e427198f27cf80274983806595799f36ccb8770a3435f746600edfe703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Apoptosis</topic><topic>Autoimmune diseases</topic><topic>Cancer</topic><topic>Drug development</topic><topic>Immune response</topic><topic>Immune system</topic><topic>Ligands</topic><topic>Tumor necrosis factor</topic><topic>Tumor necrosis factor receptors</topic><topic>Tumor necrosis factor-TNF</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dostert, Catherine</creatorcontrib><creatorcontrib>Grusdat, Melanie</creatorcontrib><creatorcontrib>Letellier, Elisabeth</creatorcontrib><creatorcontrib>Brenner, Dirk</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Physical Education Index</collection><collection>MEDLINE - Academic</collection><jtitle>Physiological reviews</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dostert, Catherine</au><au>Grusdat, Melanie</au><au>Letellier, Elisabeth</au><au>Brenner, Dirk</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The TNF Family of Ligands and Receptors: Communication Modules in the Immune System and Beyond</atitle><jtitle>Physiological reviews</jtitle><addtitle>Physiol Rev</addtitle><date>2019-01-01</date><risdate>2019</risdate><volume>99</volume><issue>1</issue><spage>115</spage><epage>160</epage><pages>115-160</pages><issn>0031-9333</issn><eissn>1522-1210</eissn><abstract>The tumor necrosis factor (TNF) and TNF receptor (TNFR) superfamilies (TNFSF/TNFRSF) include 19 ligands and 29 receptors that play important roles in the modulation of cellular functions. The communication pathways mediated by TNFSF/TNFRSF are essential for numerous developmental, homeostatic, and stimulus-responsive processes in vivo. TNFSF/TNFRSF members regulate cellular differentiation, survival, and programmed death, but their most critical functions pertain to the immune system. Both innate and adaptive immune cells are controlled by TNFSF/TNFRSF members in a manner that is crucial for the coordination of various mechanisms driving either co-stimulation or co-inhibition of the immune response. Dysregulation of these same signaling pathways has been implicated in inflammatory and autoimmune diseases, highlighting the importance of their tight regulation. Investigation of the control of TNFSF/TNFRSF activities has led to the development of therapeutics with the potential to reduce chronic inflammation or promote anti-tumor immunity. The study of TNFSF/TNFRSF proteins has exploded over the last 30 yr, but there remains a need to better understand the fundamental mechanisms underlying the molecular pathways they mediate to design more effective anti-inflammatory and anti-cancer therapies.</abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>30354964</pmid><doi>10.1152/physrev.00045.2017</doi><tpages>46</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0031-9333
ispartof Physiological reviews, 2019-01, Vol.99 (1), p.115-160
issn 0031-9333
1522-1210
language eng
recordid cdi_proquest_miscellaneous_2125308764
source American Physiological Society; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection
subjects Apoptosis
Autoimmune diseases
Cancer
Drug development
Immune response
Immune system
Ligands
Tumor necrosis factor
Tumor necrosis factor receptors
Tumor necrosis factor-TNF
title The TNF Family of Ligands and Receptors: Communication Modules in the Immune System and Beyond
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-03T11%3A16%3A09IST&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=The%20TNF%20Family%20of%20Ligands%20and%20Receptors:%20Communication%20Modules%20in%20the%20Immune%20System%20and%20Beyond&rft.jtitle=Physiological%20reviews&rft.au=Dostert,%20Catherine&rft.date=2019-01-01&rft.volume=99&rft.issue=1&rft.spage=115&rft.epage=160&rft.pages=115-160&rft.issn=0031-9333&rft.eissn=1522-1210&rft_id=info:doi/10.1152/physrev.00045.2017&rft_dat=%3Cproquest_cross%3E2125308764%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=2184203898&rft_id=info:pmid/30354964&rfr_iscdi=true