Global Transcriptome Analysis Reveals Distinct Phases of the Endothelial Response to TNF

The vascular endothelium acts as a dynamic interface between blood and tissue. TNF-α, a major regulator of inflammation, induces endothelial cell (EC) transcriptional changes, the overall response dynamics of which have not been fully elucidated. In the present study, we conducted an extended time-c...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The Journal of immunology (1950) 2024-01, Vol.212 (1), p.117-129
Hauptverfasser: Struck, Eike C, Belova, Tatiana, Hsieh, Ping-Han, Odeberg, Jacob O, Kuijjer, Marieke L, Dusart, Philip J, Butler, Lynn M
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 129
container_issue 1
container_start_page 117
container_title The Journal of immunology (1950)
container_volume 212
creator Struck, Eike C
Belova, Tatiana
Hsieh, Ping-Han
Odeberg, Jacob O
Kuijjer, Marieke L
Dusart, Philip J
Butler, Lynn M
description The vascular endothelium acts as a dynamic interface between blood and tissue. TNF-α, a major regulator of inflammation, induces endothelial cell (EC) transcriptional changes, the overall response dynamics of which have not been fully elucidated. In the present study, we conducted an extended time-course analysis of the human EC response to TNF, from 30 min to 72 h. We identified regulated genes and used weighted gene network correlation analysis to decipher coexpression profiles, uncovering two distinct temporal phases: an acute response (between 1 and 4 h) and a later phase (between 12 and 24 h). Sex-based subset analysis revealed that the response was comparable between female and male cells. Several previously uncharacterized genes were strongly regulated during the acute phase, whereas the majority in the later phase were IFN-stimulated genes. A lack of IFN transcription indicated that this IFN-stimulated gene expression was independent of de novo IFN production. We also observed two groups of genes whose transcription was inhibited by TNF: those that resolved toward baseline levels and those that did not. Our study provides insights into the global dynamics of the EC transcriptional response to TNF, highlighting distinct gene expression patterns during the acute and later phases. Data for all coding and noncoding genes is provided on the Web site (http://www.endothelial-response.org/). These findings may be useful in understanding the role of ECs in inflammation and in developing TNF signaling-targeted therapies.
doi_str_mv 10.4049/jimmunol.2300419
format Article
fullrecord <record><control><sourceid>proquest_swepu</sourceid><recordid>TN_cdi_swepub_primary_oai_swepub_ki_se_835762</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2895262500</sourcerecordid><originalsourceid>FETCH-LOGICAL-c547t-ce85b1ad783d585e9b2ba013b7b14a61ce0df508a0819dfdc268d2263a833ae33</originalsourceid><addsrcrecordid>eNp9UktvEzEQthCIhsCdE_jIZcvYXr9OKOoLpApQFRA3y7vrNG537cXeFPXf4yhJoQc4jeX5HjOaD6HXBI5rqPX7Gz8MmxD7Y8oAaqKfoBnhHCohQDxFMwBKKyKFPEIvcr4BAAG0fo6OmAKiCSUz9OOij43t8TLZkNvkxykODi-C7e-zz_jK3TnbZ3zq8-RDO-Gva5tdxnGFp7XDZ6GLpfa-KFy5PMaQHZ4iXn4-f4merQrTvdrXOfp2frY8-Vhdfrn4dLK4rFpey6lqneINsZ1UrOOKO93QxgJhjWxIbQVpHXQrDsqCIrpbdS0VqqNUMKsYs46xOap2uvmXGzeNGZMfbLo30Xqz_7otL2cU41LQgtf_xI8pdn9IByLhtWaSavFfr1P_fWFiuja309qwmhJZF_yHHb6AB9e1LkzJ9o8tH3WCX5vreGcISMa42m73dqdQTrO9gAkx2dIGJg2jQuqCeLf3SPHnxuXJDD63ru9tcHGTDVWaU0F5ocwRHMRizsmtHiYhYLZ5Moc8mX2eCuXN3xs8EA4BYr8B1dzKIg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2895262500</pqid></control><display><type>article</type><title>Global Transcriptome Analysis Reveals Distinct Phases of the Endothelial Response to TNF</title><source>MEDLINE</source><source>NORA - Norwegian Open Research Archives</source><source>SWEPUB Freely available online</source><source>Alma/SFX Local Collection</source><creator>Struck, Eike C ; Belova, Tatiana ; Hsieh, Ping-Han ; Odeberg, Jacob O ; Kuijjer, Marieke L ; Dusart, Philip J ; Butler, Lynn M</creator><creatorcontrib>Struck, Eike C ; Belova, Tatiana ; Hsieh, Ping-Han ; Odeberg, Jacob O ; Kuijjer, Marieke L ; Dusart, Philip J ; Butler, Lynn M</creatorcontrib><description>The vascular endothelium acts as a dynamic interface between blood and tissue. TNF-α, a major regulator of inflammation, induces endothelial cell (EC) transcriptional changes, the overall response dynamics of which have not been fully elucidated. In the present study, we conducted an extended time-course analysis of the human EC response to TNF, from 30 min to 72 h. We identified regulated genes and used weighted gene network correlation analysis to decipher coexpression profiles, uncovering two distinct temporal phases: an acute response (between 1 and 4 h) and a later phase (between 12 and 24 h). Sex-based subset analysis revealed that the response was comparable between female and male cells. Several previously uncharacterized genes were strongly regulated during the acute phase, whereas the majority in the later phase were IFN-stimulated genes. A lack of IFN transcription indicated that this IFN-stimulated gene expression was independent of de novo IFN production. We also observed two groups of genes whose transcription was inhibited by TNF: those that resolved toward baseline levels and those that did not. Our study provides insights into the global dynamics of the EC transcriptional response to TNF, highlighting distinct gene expression patterns during the acute and later phases. Data for all coding and noncoding genes is provided on the Web site (http://www.endothelial-response.org/). These findings may be useful in understanding the role of ECs in inflammation and in developing TNF signaling-targeted therapies.</description><identifier>ISSN: 0022-1767</identifier><identifier>ISSN: 1550-6606</identifier><identifier>EISSN: 1550-6606</identifier><identifier>DOI: 10.4049/jimmunol.2300419</identifier><identifier>PMID: 38019121</identifier><language>eng</language><publisher>United States: The American Association of Immunologists, Inc</publisher><subject>Cells, Cultured ; Endothelial Cells - metabolism ; Endothelium, Vascular - metabolism ; Female ; Gene Expression Profiling ; Humans ; Inflammation - genetics ; Inflammation - metabolism ; Male ; Medicin och hälsovetenskap ; Signal Transduction ; Systems Immunology ; Tumor Necrosis Factor-alpha - metabolism</subject><ispartof>The Journal of immunology (1950), 2024-01, Vol.212 (1), p.117-129</ispartof><rights>Copyright © 2023 The Authors.</rights><rights>info:eu-repo/semantics/openAccess</rights><rights>Copyright © 2023 The Authors 2023 Copyright © 2023 The Authors</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c547t-ce85b1ad783d585e9b2ba013b7b14a61ce0df508a0819dfdc268d2263a833ae33</citedby><cites>FETCH-LOGICAL-c547t-ce85b1ad783d585e9b2ba013b7b14a61ce0df508a0819dfdc268d2263a833ae33</cites><orcidid>0000-0001-6280-3130 ; 0000-0003-2747-3214 ; 0000-0002-2352-8217</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,552,780,784,885,26567,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38019121$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-342174$$DView record from Swedish Publication Index$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:154937296$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Struck, Eike C</creatorcontrib><creatorcontrib>Belova, Tatiana</creatorcontrib><creatorcontrib>Hsieh, Ping-Han</creatorcontrib><creatorcontrib>Odeberg, Jacob O</creatorcontrib><creatorcontrib>Kuijjer, Marieke L</creatorcontrib><creatorcontrib>Dusart, Philip J</creatorcontrib><creatorcontrib>Butler, Lynn M</creatorcontrib><title>Global Transcriptome Analysis Reveals Distinct Phases of the Endothelial Response to TNF</title><title>The Journal of immunology (1950)</title><addtitle>J Immunol</addtitle><description>The vascular endothelium acts as a dynamic interface between blood and tissue. TNF-α, a major regulator of inflammation, induces endothelial cell (EC) transcriptional changes, the overall response dynamics of which have not been fully elucidated. In the present study, we conducted an extended time-course analysis of the human EC response to TNF, from 30 min to 72 h. We identified regulated genes and used weighted gene network correlation analysis to decipher coexpression profiles, uncovering two distinct temporal phases: an acute response (between 1 and 4 h) and a later phase (between 12 and 24 h). Sex-based subset analysis revealed that the response was comparable between female and male cells. Several previously uncharacterized genes were strongly regulated during the acute phase, whereas the majority in the later phase were IFN-stimulated genes. A lack of IFN transcription indicated that this IFN-stimulated gene expression was independent of de novo IFN production. We also observed two groups of genes whose transcription was inhibited by TNF: those that resolved toward baseline levels and those that did not. Our study provides insights into the global dynamics of the EC transcriptional response to TNF, highlighting distinct gene expression patterns during the acute and later phases. Data for all coding and noncoding genes is provided on the Web site (http://www.endothelial-response.org/). These findings may be useful in understanding the role of ECs in inflammation and in developing TNF signaling-targeted therapies.</description><subject>Cells, Cultured</subject><subject>Endothelial Cells - metabolism</subject><subject>Endothelium, Vascular - metabolism</subject><subject>Female</subject><subject>Gene Expression Profiling</subject><subject>Humans</subject><subject>Inflammation - genetics</subject><subject>Inflammation - metabolism</subject><subject>Male</subject><subject>Medicin och hälsovetenskap</subject><subject>Signal Transduction</subject><subject>Systems Immunology</subject><subject>Tumor Necrosis Factor-alpha - metabolism</subject><issn>0022-1767</issn><issn>1550-6606</issn><issn>1550-6606</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>3HK</sourceid><sourceid>D8T</sourceid><recordid>eNp9UktvEzEQthCIhsCdE_jIZcvYXr9OKOoLpApQFRA3y7vrNG537cXeFPXf4yhJoQc4jeX5HjOaD6HXBI5rqPX7Gz8MmxD7Y8oAaqKfoBnhHCohQDxFMwBKKyKFPEIvcr4BAAG0fo6OmAKiCSUz9OOij43t8TLZkNvkxykODi-C7e-zz_jK3TnbZ3zq8-RDO-Gva5tdxnGFp7XDZ6GLpfa-KFy5PMaQHZ4iXn4-f4merQrTvdrXOfp2frY8-Vhdfrn4dLK4rFpey6lqneINsZ1UrOOKO93QxgJhjWxIbQVpHXQrDsqCIrpbdS0VqqNUMKsYs46xOap2uvmXGzeNGZMfbLo30Xqz_7otL2cU41LQgtf_xI8pdn9IByLhtWaSavFfr1P_fWFiuja309qwmhJZF_yHHb6AB9e1LkzJ9o8tH3WCX5vreGcISMa42m73dqdQTrO9gAkx2dIGJg2jQuqCeLf3SPHnxuXJDD63ru9tcHGTDVWaU0F5ocwRHMRizsmtHiYhYLZ5Moc8mX2eCuXN3xs8EA4BYr8B1dzKIg</recordid><startdate>20240101</startdate><enddate>20240101</enddate><creator>Struck, Eike C</creator><creator>Belova, Tatiana</creator><creator>Hsieh, Ping-Han</creator><creator>Odeberg, Jacob O</creator><creator>Kuijjer, Marieke L</creator><creator>Dusart, Philip J</creator><creator>Butler, Lynn M</creator><general>The American Association of Immunologists, Inc</general><general>AAI</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><scope>3HK</scope><scope>5PM</scope><scope>ADTPV</scope><scope>AFDQA</scope><scope>AOWAS</scope><scope>D8T</scope><scope>D8V</scope><scope>ZZAVC</scope><orcidid>https://orcid.org/0000-0001-6280-3130</orcidid><orcidid>https://orcid.org/0000-0003-2747-3214</orcidid><orcidid>https://orcid.org/0000-0002-2352-8217</orcidid></search><sort><creationdate>20240101</creationdate><title>Global Transcriptome Analysis Reveals Distinct Phases of the Endothelial Response to TNF</title><author>Struck, Eike C ; Belova, Tatiana ; Hsieh, Ping-Han ; Odeberg, Jacob O ; Kuijjer, Marieke L ; Dusart, Philip J ; Butler, Lynn M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c547t-ce85b1ad783d585e9b2ba013b7b14a61ce0df508a0819dfdc268d2263a833ae33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Cells, Cultured</topic><topic>Endothelial Cells - metabolism</topic><topic>Endothelium, Vascular - metabolism</topic><topic>Female</topic><topic>Gene Expression Profiling</topic><topic>Humans</topic><topic>Inflammation - genetics</topic><topic>Inflammation - metabolism</topic><topic>Male</topic><topic>Medicin och hälsovetenskap</topic><topic>Signal Transduction</topic><topic>Systems Immunology</topic><topic>Tumor Necrosis Factor-alpha - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Struck, Eike C</creatorcontrib><creatorcontrib>Belova, Tatiana</creatorcontrib><creatorcontrib>Hsieh, Ping-Han</creatorcontrib><creatorcontrib>Odeberg, Jacob O</creatorcontrib><creatorcontrib>Kuijjer, Marieke L</creatorcontrib><creatorcontrib>Dusart, Philip J</creatorcontrib><creatorcontrib>Butler, Lynn M</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>NORA - Norwegian Open Research Archives</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SwePub</collection><collection>SWEPUB Kungliga Tekniska Högskolan full text</collection><collection>SwePub Articles</collection><collection>SWEPUB Freely available online</collection><collection>SWEPUB Kungliga Tekniska Högskolan</collection><collection>SwePub Articles full text</collection><jtitle>The Journal of immunology (1950)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Struck, Eike C</au><au>Belova, Tatiana</au><au>Hsieh, Ping-Han</au><au>Odeberg, Jacob O</au><au>Kuijjer, Marieke L</au><au>Dusart, Philip J</au><au>Butler, Lynn M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Global Transcriptome Analysis Reveals Distinct Phases of the Endothelial Response to TNF</atitle><jtitle>The Journal of immunology (1950)</jtitle><addtitle>J Immunol</addtitle><date>2024-01-01</date><risdate>2024</risdate><volume>212</volume><issue>1</issue><spage>117</spage><epage>129</epage><pages>117-129</pages><issn>0022-1767</issn><issn>1550-6606</issn><eissn>1550-6606</eissn><abstract>The vascular endothelium acts as a dynamic interface between blood and tissue. TNF-α, a major regulator of inflammation, induces endothelial cell (EC) transcriptional changes, the overall response dynamics of which have not been fully elucidated. In the present study, we conducted an extended time-course analysis of the human EC response to TNF, from 30 min to 72 h. We identified regulated genes and used weighted gene network correlation analysis to decipher coexpression profiles, uncovering two distinct temporal phases: an acute response (between 1 and 4 h) and a later phase (between 12 and 24 h). Sex-based subset analysis revealed that the response was comparable between female and male cells. Several previously uncharacterized genes were strongly regulated during the acute phase, whereas the majority in the later phase were IFN-stimulated genes. A lack of IFN transcription indicated that this IFN-stimulated gene expression was independent of de novo IFN production. We also observed two groups of genes whose transcription was inhibited by TNF: those that resolved toward baseline levels and those that did not. Our study provides insights into the global dynamics of the EC transcriptional response to TNF, highlighting distinct gene expression patterns during the acute and later phases. Data for all coding and noncoding genes is provided on the Web site (http://www.endothelial-response.org/). These findings may be useful in understanding the role of ECs in inflammation and in developing TNF signaling-targeted therapies.</abstract><cop>United States</cop><pub>The American Association of Immunologists, Inc</pub><pmid>38019121</pmid><doi>10.4049/jimmunol.2300419</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0001-6280-3130</orcidid><orcidid>https://orcid.org/0000-0003-2747-3214</orcidid><orcidid>https://orcid.org/0000-0002-2352-8217</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0022-1767
ispartof The Journal of immunology (1950), 2024-01, Vol.212 (1), p.117-129
issn 0022-1767
1550-6606
1550-6606
language eng
recordid cdi_swepub_primary_oai_swepub_ki_se_835762
source MEDLINE; NORA - Norwegian Open Research Archives; SWEPUB Freely available online; Alma/SFX Local Collection
subjects Cells, Cultured
Endothelial Cells - metabolism
Endothelium, Vascular - metabolism
Female
Gene Expression Profiling
Humans
Inflammation - genetics
Inflammation - metabolism
Male
Medicin och hälsovetenskap
Signal Transduction
Systems Immunology
Tumor Necrosis Factor-alpha - metabolism
title Global Transcriptome Analysis Reveals Distinct Phases of the Endothelial Response to TNF
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T23%3A25%3A00IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_swepu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Global%20Transcriptome%20Analysis%20Reveals%20Distinct%20Phases%20of%20the%20Endothelial%20Response%20to%20TNF&rft.jtitle=The%20Journal%20of%20immunology%20(1950)&rft.au=Struck,%20Eike%20C&rft.date=2024-01-01&rft.volume=212&rft.issue=1&rft.spage=117&rft.epage=129&rft.pages=117-129&rft.issn=0022-1767&rft.eissn=1550-6606&rft_id=info:doi/10.4049/jimmunol.2300419&rft_dat=%3Cproquest_swepu%3E2895262500%3C/proquest_swepu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2895262500&rft_id=info:pmid/38019121&rfr_iscdi=true