Flow cytometry and gene expression profiling of immune cells of the carotid plaque and peripheral blood
Abstract Objectives The relative contribution of the local vs. peripheral inflammation to the atherothrombotic processes is unknown. We compared the inflammatory status of the immune cells of the carotid plaque with similar cells in peripheral circulation of patients with advanced carotid disease (P...
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creator | Sternberg, Zohara Ghanim, Husam Gillotti, Kristen M Tario, Joseph D Munschauer, Frederick Curl, Richard Noor, Sonya Yu, Jihnhee Ambrus, Julian L Wallace, Paul Dandona, Paresh |
description | Abstract Objectives The relative contribution of the local vs. peripheral inflammation to the atherothrombotic processes is unknown. We compared the inflammatory status of the immune cells of the carotid plaque with similar cells in peripheral circulation of patients with advanced carotid disease (PCDs). Methods Mononuclear cells (MNCs) were extracted from carotid endarterectomy (CEA) samples by enzymatic digestion and subsequent magnetic cell sorting. The cell surface antigenic expressions, and mRNA expression levels were compared between CEA MNCs and peripheral MNCs, using flow cytometry and RT-PCR techniques. Results The percentages of resting MNCs were lower, and activated MNCs, particularly monocytes, were higher in the CEAMNCs, as compared to the peripheral MNCs. The percentages of activated T cells and B cells were higher in the peripheral MNCs of PCDs, than in healthy controls (HCs), but the percentages of activated monocytes did not differ between the two groups. The expression levels of both pro-inflammatory/pro-thrombotic (P38 , JNKB-1, Egr-1 PAI-1, MCP-1, TF, MMP-9, HMGB-1, TNF-α, mTOR) and anti-inflammatory (PPAR-γ, TGF-β) mediators were significantly higher in the CEA MNCs as compared to the peripheral MNCs. Furthermore, MMP-9 and PPAR-γ expression levels were higher in the peripheral MNCs of PCDs than HCs. Conclusion The inflammatory status is higher in the immune cells of the carotid plaque, as compared to those cells in the peripheral blood. The altered expression levels of both pro-inflammatory/pro-thrombotic and anti-inflammatory mediators in the milieu of the plaque suggest that the balance between these various mediators may play a key role in carotid disease progression. |
doi_str_mv | 10.1016/j.atherosclerosis.2013.04.035 |
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We compared the inflammatory status of the immune cells of the carotid plaque with similar cells in peripheral circulation of patients with advanced carotid disease (PCDs). Methods Mononuclear cells (MNCs) were extracted from carotid endarterectomy (CEA) samples by enzymatic digestion and subsequent magnetic cell sorting. The cell surface antigenic expressions, and mRNA expression levels were compared between CEA MNCs and peripheral MNCs, using flow cytometry and RT-PCR techniques. Results The percentages of resting MNCs were lower, and activated MNCs, particularly monocytes, were higher in the CEAMNCs, as compared to the peripheral MNCs. The percentages of activated T cells and B cells were higher in the peripheral MNCs of PCDs, than in healthy controls (HCs), but the percentages of activated monocytes did not differ between the two groups. The expression levels of both pro-inflammatory/pro-thrombotic (P38 , JNKB-1, Egr-1 PAI-1, MCP-1, TF, MMP-9, HMGB-1, TNF-α, mTOR) and anti-inflammatory (PPAR-γ, TGF-β) mediators were significantly higher in the CEA MNCs as compared to the peripheral MNCs. Furthermore, MMP-9 and PPAR-γ expression levels were higher in the peripheral MNCs of PCDs than HCs. Conclusion The inflammatory status is higher in the immune cells of the carotid plaque, as compared to those cells in the peripheral blood. The altered expression levels of both pro-inflammatory/pro-thrombotic and anti-inflammatory mediators in the milieu of the plaque suggest that the balance between these various mediators may play a key role in carotid disease progression.</description><identifier>ISSN: 0021-9150</identifier><identifier>EISSN: 1879-1484</identifier><identifier>DOI: 10.1016/j.atherosclerosis.2013.04.035</identifier><identifier>PMID: 23880185</identifier><language>eng</language><publisher>Ireland: Elsevier Ireland Ltd</publisher><subject>Aged ; Aged, 80 and over ; atherosclerosis ; B-Lymphocytes - cytology ; B-Lymphocytes - immunology ; Cardiovascular ; Carotid stenosis ; Carotid Stenosis - genetics ; Carotid Stenosis - immunology ; Carotid Stenosis - pathology ; Cell adhesion ; Cell Adhesion - immunology ; Cell surface markers ; disease course ; Female ; Flow Cytometry ; Gene expression ; Humans ; Immunomagnetic Separation ; Immunophenotyping ; inflammation ; Leukocytes, Mononuclear - cytology ; Leukocytes, Mononuclear - immunology ; Male ; messenger RNA ; Middle Aged ; monocytes ; Monocytes - cytology ; Monocytes - immunology ; Mononuclear cells ; patients ; reverse transcriptase polymerase chain reaction ; sorting ; T-lymphocytes ; T-Lymphocytes - cytology ; T-Lymphocytes - immunology ; Thrombosis ; Thrombosis - genetics ; Thrombosis - immunology ; Thrombosis - pathology ; Transcriptome - immunology ; transforming growth factor beta ; tumor necrosis factor-alpha ; Vasculitis - genetics ; Vasculitis - immunology ; Vasculitis - pathology</subject><ispartof>Atherosclerosis, 2013-08, Vol.229 (2), p.338-347</ispartof><rights>2013</rights><rights>Published by Elsevier Ireland Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c534t-5e8a72d03e58f5a95eefb3d1b73d7bdba4f857160a50d80be3b552a07bb9d14a3</citedby><cites>FETCH-LOGICAL-c534t-5e8a72d03e58f5a95eefb3d1b73d7bdba4f857160a50d80be3b552a07bb9d14a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.atherosclerosis.2013.04.035$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27929,27930,46000</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23880185$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sternberg, Zohara</creatorcontrib><creatorcontrib>Ghanim, Husam</creatorcontrib><creatorcontrib>Gillotti, Kristen M</creatorcontrib><creatorcontrib>Tario, Joseph D</creatorcontrib><creatorcontrib>Munschauer, Frederick</creatorcontrib><creatorcontrib>Curl, Richard</creatorcontrib><creatorcontrib>Noor, Sonya</creatorcontrib><creatorcontrib>Yu, Jihnhee</creatorcontrib><creatorcontrib>Ambrus, Julian L</creatorcontrib><creatorcontrib>Wallace, Paul</creatorcontrib><creatorcontrib>Dandona, Paresh</creatorcontrib><title>Flow cytometry and gene expression profiling of immune cells of the carotid plaque and peripheral blood</title><title>Atherosclerosis</title><addtitle>Atherosclerosis</addtitle><description>Abstract Objectives The relative contribution of the local vs. peripheral inflammation to the atherothrombotic processes is unknown. We compared the inflammatory status of the immune cells of the carotid plaque with similar cells in peripheral circulation of patients with advanced carotid disease (PCDs). Methods Mononuclear cells (MNCs) were extracted from carotid endarterectomy (CEA) samples by enzymatic digestion and subsequent magnetic cell sorting. The cell surface antigenic expressions, and mRNA expression levels were compared between CEA MNCs and peripheral MNCs, using flow cytometry and RT-PCR techniques. Results The percentages of resting MNCs were lower, and activated MNCs, particularly monocytes, were higher in the CEAMNCs, as compared to the peripheral MNCs. The percentages of activated T cells and B cells were higher in the peripheral MNCs of PCDs, than in healthy controls (HCs), but the percentages of activated monocytes did not differ between the two groups. The expression levels of both pro-inflammatory/pro-thrombotic (P38 , JNKB-1, Egr-1 PAI-1, MCP-1, TF, MMP-9, HMGB-1, TNF-α, mTOR) and anti-inflammatory (PPAR-γ, TGF-β) mediators were significantly higher in the CEA MNCs as compared to the peripheral MNCs. Furthermore, MMP-9 and PPAR-γ expression levels were higher in the peripheral MNCs of PCDs than HCs. Conclusion The inflammatory status is higher in the immune cells of the carotid plaque, as compared to those cells in the peripheral blood. The altered expression levels of both pro-inflammatory/pro-thrombotic and anti-inflammatory mediators in the milieu of the plaque suggest that the balance between these various mediators may play a key role in carotid disease progression.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>atherosclerosis</subject><subject>B-Lymphocytes - cytology</subject><subject>B-Lymphocytes - immunology</subject><subject>Cardiovascular</subject><subject>Carotid stenosis</subject><subject>Carotid Stenosis - genetics</subject><subject>Carotid Stenosis - immunology</subject><subject>Carotid Stenosis - pathology</subject><subject>Cell adhesion</subject><subject>Cell Adhesion - immunology</subject><subject>Cell surface markers</subject><subject>disease course</subject><subject>Female</subject><subject>Flow Cytometry</subject><subject>Gene expression</subject><subject>Humans</subject><subject>Immunomagnetic Separation</subject><subject>Immunophenotyping</subject><subject>inflammation</subject><subject>Leukocytes, Mononuclear - cytology</subject><subject>Leukocytes, Mononuclear - immunology</subject><subject>Male</subject><subject>messenger RNA</subject><subject>Middle Aged</subject><subject>monocytes</subject><subject>Monocytes - cytology</subject><subject>Monocytes - immunology</subject><subject>Mononuclear cells</subject><subject>patients</subject><subject>reverse transcriptase polymerase chain reaction</subject><subject>sorting</subject><subject>T-lymphocytes</subject><subject>T-Lymphocytes - cytology</subject><subject>T-Lymphocytes - immunology</subject><subject>Thrombosis</subject><subject>Thrombosis - genetics</subject><subject>Thrombosis - immunology</subject><subject>Thrombosis - pathology</subject><subject>Transcriptome - immunology</subject><subject>transforming growth factor beta</subject><subject>tumor necrosis factor-alpha</subject><subject>Vasculitis - genetics</subject><subject>Vasculitis - immunology</subject><subject>Vasculitis - pathology</subject><issn>0021-9150</issn><issn>1879-1484</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkktv1DAUhS0EokPhL4A3SGwSruO48SxAqqq2IFViUbq2_LgZPDhxsBNg_n0dprDoio0f8rnHR9-9hLxlUDNgZ-_3tZ6_YYrZhnX1uW6A8RraGrh4QjZMdtuKtbJ9SjYADau2TMAJeZHzHgDajsnn5KThUgKTYkN2VyH-ovYwxwHndKB6dHSHI1L8PSXM2ceRTin2PvhxR2NP_TAs5dliCHm9lzDU6hRn7-gU9I8F_3hMmPxUcupATYjRvSTPeh0yvnrYT8nd1eXXi0_VzZfrzxfnN5UVvJ0rgVJ3jQOOQvZCbwVib7hjpuOuM87otpeiY2egBTgJBrkRotHQGbN1rNX8lLw7-pbQJUue1eDzGlaPGJesWMsaURxYW6QfjlJbOOaEvZqSH3Q6KAZqZa326hFrtbJW0KrCutS_fvhqMQO6f9V_4RbBm6Og11HpXSr1d7fFQayNKG1piuL6qMCC5KfHpLL1OFp0PqGdlYv-v8N8fORkS8e81eE7HjDv45LGwl0xlRsF6nYdjXUyGC-nruP8Hu3Tufg</recordid><startdate>20130801</startdate><enddate>20130801</enddate><creator>Sternberg, Zohara</creator><creator>Ghanim, Husam</creator><creator>Gillotti, Kristen M</creator><creator>Tario, Joseph D</creator><creator>Munschauer, Frederick</creator><creator>Curl, Richard</creator><creator>Noor, Sonya</creator><creator>Yu, Jihnhee</creator><creator>Ambrus, Julian L</creator><creator>Wallace, Paul</creator><creator>Dandona, Paresh</creator><general>Elsevier Ireland Ltd</general><scope>FBQ</scope><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>20130801</creationdate><title>Flow cytometry and gene expression profiling of immune cells of the carotid plaque and peripheral blood</title><author>Sternberg, Zohara ; Ghanim, Husam ; Gillotti, Kristen M ; Tario, Joseph D ; Munschauer, Frederick ; Curl, Richard ; Noor, Sonya ; Yu, Jihnhee ; Ambrus, Julian L ; Wallace, Paul ; Dandona, Paresh</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c534t-5e8a72d03e58f5a95eefb3d1b73d7bdba4f857160a50d80be3b552a07bb9d14a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>atherosclerosis</topic><topic>B-Lymphocytes - cytology</topic><topic>B-Lymphocytes - immunology</topic><topic>Cardiovascular</topic><topic>Carotid stenosis</topic><topic>Carotid Stenosis - genetics</topic><topic>Carotid Stenosis - immunology</topic><topic>Carotid Stenosis - pathology</topic><topic>Cell adhesion</topic><topic>Cell Adhesion - immunology</topic><topic>Cell surface markers</topic><topic>disease course</topic><topic>Female</topic><topic>Flow Cytometry</topic><topic>Gene expression</topic><topic>Humans</topic><topic>Immunomagnetic Separation</topic><topic>Immunophenotyping</topic><topic>inflammation</topic><topic>Leukocytes, Mononuclear - cytology</topic><topic>Leukocytes, Mononuclear - immunology</topic><topic>Male</topic><topic>messenger RNA</topic><topic>Middle Aged</topic><topic>monocytes</topic><topic>Monocytes - cytology</topic><topic>Monocytes - immunology</topic><topic>Mononuclear cells</topic><topic>patients</topic><topic>reverse transcriptase polymerase chain reaction</topic><topic>sorting</topic><topic>T-lymphocytes</topic><topic>T-Lymphocytes - cytology</topic><topic>T-Lymphocytes - immunology</topic><topic>Thrombosis</topic><topic>Thrombosis - genetics</topic><topic>Thrombosis - immunology</topic><topic>Thrombosis - pathology</topic><topic>Transcriptome - immunology</topic><topic>transforming growth factor beta</topic><topic>tumor necrosis factor-alpha</topic><topic>Vasculitis - genetics</topic><topic>Vasculitis - immunology</topic><topic>Vasculitis - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sternberg, Zohara</creatorcontrib><creatorcontrib>Ghanim, Husam</creatorcontrib><creatorcontrib>Gillotti, Kristen M</creatorcontrib><creatorcontrib>Tario, Joseph D</creatorcontrib><creatorcontrib>Munschauer, Frederick</creatorcontrib><creatorcontrib>Curl, Richard</creatorcontrib><creatorcontrib>Noor, Sonya</creatorcontrib><creatorcontrib>Yu, Jihnhee</creatorcontrib><creatorcontrib>Ambrus, Julian L</creatorcontrib><creatorcontrib>Wallace, Paul</creatorcontrib><creatorcontrib>Dandona, Paresh</creatorcontrib><collection>AGRIS</collection><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>Atherosclerosis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sternberg, Zohara</au><au>Ghanim, Husam</au><au>Gillotti, Kristen M</au><au>Tario, Joseph D</au><au>Munschauer, Frederick</au><au>Curl, Richard</au><au>Noor, Sonya</au><au>Yu, Jihnhee</au><au>Ambrus, Julian L</au><au>Wallace, Paul</au><au>Dandona, Paresh</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Flow cytometry and gene expression profiling of immune cells of the carotid plaque and peripheral blood</atitle><jtitle>Atherosclerosis</jtitle><addtitle>Atherosclerosis</addtitle><date>2013-08-01</date><risdate>2013</risdate><volume>229</volume><issue>2</issue><spage>338</spage><epage>347</epage><pages>338-347</pages><issn>0021-9150</issn><eissn>1879-1484</eissn><abstract>Abstract Objectives The relative contribution of the local vs. peripheral inflammation to the atherothrombotic processes is unknown. We compared the inflammatory status of the immune cells of the carotid plaque with similar cells in peripheral circulation of patients with advanced carotid disease (PCDs). Methods Mononuclear cells (MNCs) were extracted from carotid endarterectomy (CEA) samples by enzymatic digestion and subsequent magnetic cell sorting. The cell surface antigenic expressions, and mRNA expression levels were compared between CEA MNCs and peripheral MNCs, using flow cytometry and RT-PCR techniques. Results The percentages of resting MNCs were lower, and activated MNCs, particularly monocytes, were higher in the CEAMNCs, as compared to the peripheral MNCs. The percentages of activated T cells and B cells were higher in the peripheral MNCs of PCDs, than in healthy controls (HCs), but the percentages of activated monocytes did not differ between the two groups. The expression levels of both pro-inflammatory/pro-thrombotic (P38 , JNKB-1, Egr-1 PAI-1, MCP-1, TF, MMP-9, HMGB-1, TNF-α, mTOR) and anti-inflammatory (PPAR-γ, TGF-β) mediators were significantly higher in the CEA MNCs as compared to the peripheral MNCs. Furthermore, MMP-9 and PPAR-γ expression levels were higher in the peripheral MNCs of PCDs than HCs. Conclusion The inflammatory status is higher in the immune cells of the carotid plaque, as compared to those cells in the peripheral blood. The altered expression levels of both pro-inflammatory/pro-thrombotic and anti-inflammatory mediators in the milieu of the plaque suggest that the balance between these various mediators may play a key role in carotid disease progression.</abstract><cop>Ireland</cop><pub>Elsevier Ireland Ltd</pub><pmid>23880185</pmid><doi>10.1016/j.atherosclerosis.2013.04.035</doi><tpages>10</tpages></addata></record> |
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subjects | Aged Aged, 80 and over atherosclerosis B-Lymphocytes - cytology B-Lymphocytes - immunology Cardiovascular Carotid stenosis Carotid Stenosis - genetics Carotid Stenosis - immunology Carotid Stenosis - pathology Cell adhesion Cell Adhesion - immunology Cell surface markers disease course Female Flow Cytometry Gene expression Humans Immunomagnetic Separation Immunophenotyping inflammation Leukocytes, Mononuclear - cytology Leukocytes, Mononuclear - immunology Male messenger RNA Middle Aged monocytes Monocytes - cytology Monocytes - immunology Mononuclear cells patients reverse transcriptase polymerase chain reaction sorting T-lymphocytes T-Lymphocytes - cytology T-Lymphocytes - immunology Thrombosis Thrombosis - genetics Thrombosis - immunology Thrombosis - pathology Transcriptome - immunology transforming growth factor beta tumor necrosis factor-alpha Vasculitis - genetics Vasculitis - immunology Vasculitis - pathology |
title | Flow cytometry and gene expression profiling of immune cells of the carotid plaque and peripheral blood |
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