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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Veröffentlicht in:Atherosclerosis 2013-08, Vol.229 (2), p.338-347
Hauptverfasser: 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
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container_end_page 347
container_issue 2
container_start_page 338
container_title Atherosclerosis
container_volume 229
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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