Inflammasome Signaling and Impaired Vascular Health in Psoriasis
OBJECTIVE—Psoriasis is an inflammatory skin disease which heightens the risk of cardiovascular disease. This study directly investigated vascular endothelial health and systemically altered pathways in psoriasis and matched controls. APPROACH AND RESULTS—Twenty patients (mean age, 40 years; 50% male...
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Veröffentlicht in: | Arteriosclerosis, thrombosis, and vascular biology thrombosis, and vascular biology, 2019-04, Vol.39 (4), p.787-798 |
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creator | Garshick, Michael S Barrett, Tessa J Wechter, Todd Azarchi, Sarah Scher, Jose U Neimann, Andrea Katz, Stuart Fuentes-Duculan, Judilyn Cannizzaro, Maria V Jelic, Sanja Fisher, Edward A Krueger, James G Berger, Jeffrey S |
description | OBJECTIVE—Psoriasis is an inflammatory skin disease which heightens the risk of cardiovascular disease. This study directly investigated vascular endothelial health and systemically altered pathways in psoriasis and matched controls.
APPROACH AND RESULTS—Twenty patients (mean age, 40 years; 50% male) with active psoriasis and 10 age-, sex-matched controls were recruited. To investigate systemically alerted pathways, a deep sequencing omics approach was applied, including unbiased blood transcriptomic and targeted proteomic analysis. Vascular endothelial health was assessed by transcriptomic profiling of endothelial cells obtained from the brachial veins of recruited participants. Blood transcriptomic profiling identified inflammasome signaling as the highest differentially expressed canonical pathway (Z score 1.6; P=1×10) including upregulation of CASP5 and interleukin (IL)-1β. Proteomic panels revealed IL-6 as a top differentially expressed cytokine in psoriasis with pathway analysis highlighting IL-1β (Z score 3.7; P=1.02×10) as an upstream activator of the observed upregulated proteins. Direct profiling of harvested brachial vein endothelial cells demonstrated inflammatory transcript (eg, IL-1β, CXCL10, VCAM-1, IL-8, CXCL1, Lymphotoxin beta, ICAM-1, COX-2, and CCL3) upregulation between psoriasis versus controls. A linear relationship was seen between differentially expressed endothelial inflammatory transcripts and psoriasis disease severity. IL-6 levels correlated with inflammatory endothelial cell transcripts and whole blood inflammasome-associated transcripts, including CASP5 and IL-1β.
CONCLUSIONS—An unbiased sequencing approach demonstrated the inflammasome as the most differentially altered pathway in psoriasis versus controls. Inflammasome signaling correlated with psoriasis disease severity, circulating IL-6, and proinflammatory endothelial transcripts. These findings help better explain the heightened risk of cardiovascular disease in psoriasis.
CLINICAL TRIAL REGISTRATION—URLhttp://www.clinicaltrials.gov. Unique identifierNCT03228017. |
doi_str_mv | 10.1161/ATVBAHA.118.312246 |
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APPROACH AND RESULTS—Twenty patients (mean age, 40 years; 50% male) with active psoriasis and 10 age-, sex-matched controls were recruited. To investigate systemically alerted pathways, a deep sequencing omics approach was applied, including unbiased blood transcriptomic and targeted proteomic analysis. Vascular endothelial health was assessed by transcriptomic profiling of endothelial cells obtained from the brachial veins of recruited participants. Blood transcriptomic profiling identified inflammasome signaling as the highest differentially expressed canonical pathway (Z score 1.6; P=1×10) including upregulation of CASP5 and interleukin (IL)-1β. Proteomic panels revealed IL-6 as a top differentially expressed cytokine in psoriasis with pathway analysis highlighting IL-1β (Z score 3.7; P=1.02×10) as an upstream activator of the observed upregulated proteins. Direct profiling of harvested brachial vein endothelial cells demonstrated inflammatory transcript (eg, IL-1β, CXCL10, VCAM-1, IL-8, CXCL1, Lymphotoxin beta, ICAM-1, COX-2, and CCL3) upregulation between psoriasis versus controls. A linear relationship was seen between differentially expressed endothelial inflammatory transcripts and psoriasis disease severity. IL-6 levels correlated with inflammatory endothelial cell transcripts and whole blood inflammasome-associated transcripts, including CASP5 and IL-1β.
CONCLUSIONS—An unbiased sequencing approach demonstrated the inflammasome as the most differentially altered pathway in psoriasis versus controls. Inflammasome signaling correlated with psoriasis disease severity, circulating IL-6, and proinflammatory endothelial transcripts. These findings help better explain the heightened risk of cardiovascular disease in psoriasis.
CLINICAL TRIAL REGISTRATION—URLhttp://www.clinicaltrials.gov. Unique identifierNCT03228017.</description><identifier>ISSN: 1079-5642</identifier><identifier>EISSN: 1524-4636</identifier><identifier>DOI: 10.1161/ATVBAHA.118.312246</identifier><identifier>PMID: 30760013</identifier><language>eng</language><publisher>United States: American Heart Association, Inc</publisher><subject>Adult ; Aorta - cytology ; Cell Adhesion Molecules - biosynthesis ; Cell Adhesion Molecules - genetics ; Cells, Cultured ; Cytokines - biosynthesis ; Cytokines - genetics ; Endothelial Cells - drug effects ; Endothelial Cells - physiology ; Female ; Gene Expression Profiling ; Humans ; Inflammasomes - metabolism ; Inflammasomes - physiology ; Male ; Middle Aged ; NF-kappa B - metabolism ; Proteome ; Psoriasis - blood ; Psoriasis - physiopathology ; Receptors, Cytokine - biosynthesis ; Receptors, Cytokine - genetics ; RNA, Messenger - biosynthesis ; Signal Transduction ; Transcription, Genetic ; Transcriptome</subject><ispartof>Arteriosclerosis, thrombosis, and vascular biology, 2019-04, Vol.39 (4), p.787-798</ispartof><rights>2019 American Heart Association, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5646-234f7e30d993457c73d9d29597e94d879d334e75ce252bc65a9fb34a0245e8f63</citedby><cites>FETCH-LOGICAL-c5646-234f7e30d993457c73d9d29597e94d879d334e75ce252bc65a9fb34a0245e8f63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30760013$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Garshick, Michael S</creatorcontrib><creatorcontrib>Barrett, Tessa J</creatorcontrib><creatorcontrib>Wechter, Todd</creatorcontrib><creatorcontrib>Azarchi, Sarah</creatorcontrib><creatorcontrib>Scher, Jose U</creatorcontrib><creatorcontrib>Neimann, Andrea</creatorcontrib><creatorcontrib>Katz, Stuart</creatorcontrib><creatorcontrib>Fuentes-Duculan, Judilyn</creatorcontrib><creatorcontrib>Cannizzaro, Maria V</creatorcontrib><creatorcontrib>Jelic, Sanja</creatorcontrib><creatorcontrib>Fisher, Edward A</creatorcontrib><creatorcontrib>Krueger, James G</creatorcontrib><creatorcontrib>Berger, Jeffrey S</creatorcontrib><title>Inflammasome Signaling and Impaired Vascular Health in Psoriasis</title><title>Arteriosclerosis, thrombosis, and vascular biology</title><addtitle>Arterioscler Thromb Vasc Biol</addtitle><description>OBJECTIVE—Psoriasis is an inflammatory skin disease which heightens the risk of cardiovascular disease. This study directly investigated vascular endothelial health and systemically altered pathways in psoriasis and matched controls.
APPROACH AND RESULTS—Twenty patients (mean age, 40 years; 50% male) with active psoriasis and 10 age-, sex-matched controls were recruited. To investigate systemically alerted pathways, a deep sequencing omics approach was applied, including unbiased blood transcriptomic and targeted proteomic analysis. Vascular endothelial health was assessed by transcriptomic profiling of endothelial cells obtained from the brachial veins of recruited participants. Blood transcriptomic profiling identified inflammasome signaling as the highest differentially expressed canonical pathway (Z score 1.6; P=1×10) including upregulation of CASP5 and interleukin (IL)-1β. Proteomic panels revealed IL-6 as a top differentially expressed cytokine in psoriasis with pathway analysis highlighting IL-1β (Z score 3.7; P=1.02×10) as an upstream activator of the observed upregulated proteins. Direct profiling of harvested brachial vein endothelial cells demonstrated inflammatory transcript (eg, IL-1β, CXCL10, VCAM-1, IL-8, CXCL1, Lymphotoxin beta, ICAM-1, COX-2, and CCL3) upregulation between psoriasis versus controls. A linear relationship was seen between differentially expressed endothelial inflammatory transcripts and psoriasis disease severity. IL-6 levels correlated with inflammatory endothelial cell transcripts and whole blood inflammasome-associated transcripts, including CASP5 and IL-1β.
CONCLUSIONS—An unbiased sequencing approach demonstrated the inflammasome as the most differentially altered pathway in psoriasis versus controls. Inflammasome signaling correlated with psoriasis disease severity, circulating IL-6, and proinflammatory endothelial transcripts. These findings help better explain the heightened risk of cardiovascular disease in psoriasis.
CLINICAL TRIAL REGISTRATION—URLhttp://www.clinicaltrials.gov. Unique identifierNCT03228017.</description><subject>Adult</subject><subject>Aorta - cytology</subject><subject>Cell Adhesion Molecules - biosynthesis</subject><subject>Cell Adhesion Molecules - genetics</subject><subject>Cells, Cultured</subject><subject>Cytokines - biosynthesis</subject><subject>Cytokines - genetics</subject><subject>Endothelial Cells - drug effects</subject><subject>Endothelial Cells - physiology</subject><subject>Female</subject><subject>Gene Expression Profiling</subject><subject>Humans</subject><subject>Inflammasomes - metabolism</subject><subject>Inflammasomes - physiology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>NF-kappa B - metabolism</subject><subject>Proteome</subject><subject>Psoriasis - blood</subject><subject>Psoriasis - physiopathology</subject><subject>Receptors, Cytokine - biosynthesis</subject><subject>Receptors, Cytokine - genetics</subject><subject>RNA, Messenger - biosynthesis</subject><subject>Signal Transduction</subject><subject>Transcription, Genetic</subject><subject>Transcriptome</subject><issn>1079-5642</issn><issn>1524-4636</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE9PwkAQxTdGI4h-AQ-mRy_F_d_uxYhEhYREE5HrZmmnsLptcZdK_PZWQaMXTzOTefPm5YfQKcF9QiS5GExn14PRoB3SPiOUcrmHukRQHnPJ5H7b40TFQnLaQUchPGOMOaX4EHUYTiTGhHXR1bgqnClLE-oSoke7qIyz1SIyVR6Ny5WxHvJoZkLWOOOjERi3Xka2ih5C7a0JNhyjg8K4ACe72kNPtzfT4Sie3N-Nh4NJnLUBZEwZLxJgOFeKcZFkCctVTpVQCSiep4nKGeOQiAyooPNMCqOKOeMGUy4gLSTrocut76qZl5BnUK29cXrlbWn8u66N1X83lV3qRf2mJWdSqbQ1ON8Z-Pq1gbDWpQ0ZOGcqqJugKUmFEExQ2krpVpr5OgQPxc8bgvUner1D3w6p3qJvj85-B_w5-WbdCuRWsKndGnx4cc0GvF5-Mf3P-QMxH5Cg</recordid><startdate>201904</startdate><enddate>201904</enddate><creator>Garshick, Michael S</creator><creator>Barrett, Tessa J</creator><creator>Wechter, Todd</creator><creator>Azarchi, Sarah</creator><creator>Scher, Jose U</creator><creator>Neimann, Andrea</creator><creator>Katz, Stuart</creator><creator>Fuentes-Duculan, Judilyn</creator><creator>Cannizzaro, Maria V</creator><creator>Jelic, Sanja</creator><creator>Fisher, Edward A</creator><creator>Krueger, James G</creator><creator>Berger, Jeffrey S</creator><general>American Heart Association, Inc</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>5PM</scope></search><sort><creationdate>201904</creationdate><title>Inflammasome Signaling and Impaired Vascular Health in Psoriasis</title><author>Garshick, Michael S ; Barrett, Tessa J ; Wechter, Todd ; Azarchi, Sarah ; Scher, Jose U ; Neimann, Andrea ; Katz, Stuart ; Fuentes-Duculan, Judilyn ; Cannizzaro, Maria V ; Jelic, Sanja ; Fisher, Edward A ; Krueger, James G ; Berger, Jeffrey S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5646-234f7e30d993457c73d9d29597e94d879d334e75ce252bc65a9fb34a0245e8f63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adult</topic><topic>Aorta - cytology</topic><topic>Cell Adhesion Molecules - biosynthesis</topic><topic>Cell Adhesion Molecules - genetics</topic><topic>Cells, Cultured</topic><topic>Cytokines - biosynthesis</topic><topic>Cytokines - genetics</topic><topic>Endothelial Cells - drug effects</topic><topic>Endothelial Cells - physiology</topic><topic>Female</topic><topic>Gene Expression Profiling</topic><topic>Humans</topic><topic>Inflammasomes - metabolism</topic><topic>Inflammasomes - physiology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>NF-kappa B - metabolism</topic><topic>Proteome</topic><topic>Psoriasis - blood</topic><topic>Psoriasis - physiopathology</topic><topic>Receptors, Cytokine - biosynthesis</topic><topic>Receptors, Cytokine - genetics</topic><topic>RNA, Messenger - biosynthesis</topic><topic>Signal Transduction</topic><topic>Transcription, Genetic</topic><topic>Transcriptome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Garshick, Michael S</creatorcontrib><creatorcontrib>Barrett, Tessa J</creatorcontrib><creatorcontrib>Wechter, Todd</creatorcontrib><creatorcontrib>Azarchi, Sarah</creatorcontrib><creatorcontrib>Scher, Jose U</creatorcontrib><creatorcontrib>Neimann, Andrea</creatorcontrib><creatorcontrib>Katz, Stuart</creatorcontrib><creatorcontrib>Fuentes-Duculan, Judilyn</creatorcontrib><creatorcontrib>Cannizzaro, Maria V</creatorcontrib><creatorcontrib>Jelic, Sanja</creatorcontrib><creatorcontrib>Fisher, Edward A</creatorcontrib><creatorcontrib>Krueger, James G</creatorcontrib><creatorcontrib>Berger, Jeffrey S</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>PubMed Central (Full Participant titles)</collection><jtitle>Arteriosclerosis, thrombosis, and vascular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Garshick, Michael S</au><au>Barrett, Tessa J</au><au>Wechter, Todd</au><au>Azarchi, Sarah</au><au>Scher, Jose U</au><au>Neimann, Andrea</au><au>Katz, Stuart</au><au>Fuentes-Duculan, Judilyn</au><au>Cannizzaro, Maria V</au><au>Jelic, Sanja</au><au>Fisher, Edward A</au><au>Krueger, James G</au><au>Berger, Jeffrey S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inflammasome Signaling and Impaired Vascular Health in Psoriasis</atitle><jtitle>Arteriosclerosis, thrombosis, and vascular biology</jtitle><addtitle>Arterioscler Thromb Vasc Biol</addtitle><date>2019-04</date><risdate>2019</risdate><volume>39</volume><issue>4</issue><spage>787</spage><epage>798</epage><pages>787-798</pages><issn>1079-5642</issn><eissn>1524-4636</eissn><abstract>OBJECTIVE—Psoriasis is an inflammatory skin disease which heightens the risk of cardiovascular disease. This study directly investigated vascular endothelial health and systemically altered pathways in psoriasis and matched controls.
APPROACH AND RESULTS—Twenty patients (mean age, 40 years; 50% male) with active psoriasis and 10 age-, sex-matched controls were recruited. To investigate systemically alerted pathways, a deep sequencing omics approach was applied, including unbiased blood transcriptomic and targeted proteomic analysis. Vascular endothelial health was assessed by transcriptomic profiling of endothelial cells obtained from the brachial veins of recruited participants. Blood transcriptomic profiling identified inflammasome signaling as the highest differentially expressed canonical pathway (Z score 1.6; P=1×10) including upregulation of CASP5 and interleukin (IL)-1β. Proteomic panels revealed IL-6 as a top differentially expressed cytokine in psoriasis with pathway analysis highlighting IL-1β (Z score 3.7; P=1.02×10) as an upstream activator of the observed upregulated proteins. Direct profiling of harvested brachial vein endothelial cells demonstrated inflammatory transcript (eg, IL-1β, CXCL10, VCAM-1, IL-8, CXCL1, Lymphotoxin beta, ICAM-1, COX-2, and CCL3) upregulation between psoriasis versus controls. A linear relationship was seen between differentially expressed endothelial inflammatory transcripts and psoriasis disease severity. IL-6 levels correlated with inflammatory endothelial cell transcripts and whole blood inflammasome-associated transcripts, including CASP5 and IL-1β.
CONCLUSIONS—An unbiased sequencing approach demonstrated the inflammasome as the most differentially altered pathway in psoriasis versus controls. Inflammasome signaling correlated with psoriasis disease severity, circulating IL-6, and proinflammatory endothelial transcripts. These findings help better explain the heightened risk of cardiovascular disease in psoriasis.
CLINICAL TRIAL REGISTRATION—URLhttp://www.clinicaltrials.gov. Unique identifierNCT03228017.</abstract><cop>United States</cop><pub>American Heart Association, Inc</pub><pmid>30760013</pmid><doi>10.1161/ATVBAHA.118.312246</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aorta - cytology Cell Adhesion Molecules - biosynthesis Cell Adhesion Molecules - genetics Cells, Cultured Cytokines - biosynthesis Cytokines - genetics Endothelial Cells - drug effects Endothelial Cells - physiology Female Gene Expression Profiling Humans Inflammasomes - metabolism Inflammasomes - physiology Male Middle Aged NF-kappa B - metabolism Proteome Psoriasis - blood Psoriasis - physiopathology Receptors, Cytokine - biosynthesis Receptors, Cytokine - genetics RNA, Messenger - biosynthesis Signal Transduction Transcription, Genetic Transcriptome |
title | Inflammasome Signaling and Impaired Vascular Health in Psoriasis |
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