Oxidized low-density lipoproteins induce tissue factor expression in T-lymphocytes via activation of lectin-like oxidized low-density lipoprotein receptor-1

Abstract Aims T-lymphocytes plays an important role in the pathophysiology of acute coronary syndromes. T-cell activation in vitro by pro-inflammatory cytokines may lead to functional tissue factor (TF) expression, indicating a possible contribution of immunity to thrombosis. Oxidized low-density li...

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Veröffentlicht in:Cardiovascular research 2020-05, Vol.116 (6), p.1125-1135
Hauptverfasser: Cimmino, Giovanni, Cirillo, Plinio, Conte, Stefano, Pellegrino, Grazia, Barra, Giusi, Maresca, Lucio, Morello, Andrea, Calì, Gaetano, Loffredo, Francesco, De Palma, Raffaele, Arena, Giulia, Sawamura, Tatsuya, Ambrosio, Giuseppe, Golino, Paolo
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container_end_page 1135
container_issue 6
container_start_page 1125
container_title Cardiovascular research
container_volume 116
creator Cimmino, Giovanni
Cirillo, Plinio
Conte, Stefano
Pellegrino, Grazia
Barra, Giusi
Maresca, Lucio
Morello, Andrea
Calì, Gaetano
Loffredo, Francesco
De Palma, Raffaele
Arena, Giulia
Sawamura, Tatsuya
Ambrosio, Giuseppe
Golino, Paolo
description Abstract Aims T-lymphocytes plays an important role in the pathophysiology of acute coronary syndromes. T-cell activation in vitro by pro-inflammatory cytokines may lead to functional tissue factor (TF) expression, indicating a possible contribution of immunity to thrombosis. Oxidized low-density lipoproteins (oxLDLs) are found abundantly in atherosclerotic plaques. We aimed at evaluating the effects of oxLDLs on TF expression in T cells and the role of the lectin-like oxidized low-density lipoprotein receptor-1 (LOX-1). Methods and results CD3+ cells were isolated from healthy volunteers. Gene, protein, and surface expression of TF, as well as of LOX-1, were assessed at different time-points after oxLDL stimulation. To determine whether oxLDL-induced TF was LOX-1 dependent, T cells were pre-incubated with an LOX-1 inhibiting peptide (L-RBP) or with an anti-LOX-1 blocking antibody. To exclude that TF expression was mediated by reactive oxygen species (ROS) generation, oxLDL-stimulated T cells were pre-incubated with superoxide dismutase + catalase or with 4-Hydroxy-2,2,6,6-tetramethylpiperidine-1-oxyl (Tempol), an intracellular free radical scavenger. Finally, to determine if the observed findings in vitro may have a biological relevance, the presence of CD3+/TF+/LOX-1+ cells was evaluated by immunofluorescence in human carotid atherosclerotic lesions. oxLDLs induced functionally active TF expression in T cells in a dose- and time-dependent manner, independently on ROS generation. No effect was observed in native LDL-treated T cells. LOX-1 expression was also induced by oxLDLs in a time- and dose-dependent manner. Pre-incubation with L-RBP or anti-LOX-1 antibody almost completely inhibited oxLDL-mediated TF expression. Interestingly, human carotid plaques showed significant infiltration of CD3+ cells (mainly CD8+ cells), some of which were positive for both TF and LOX-1. Conclusion oxLDLs induce functional TF expression in T-lymphocytes in vitro via interaction of oxLDLs with LOX-1. Human carotid atherosclerotic plaques contain CD3+/CD8+cells that express both TF and LOX-1, indicating that also in patients these mechanisms may play an important role. Graphical Abstract Graphical Abstract
doi_str_mv 10.1093/cvr/cvz230
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T-cell activation in vitro by pro-inflammatory cytokines may lead to functional tissue factor (TF) expression, indicating a possible contribution of immunity to thrombosis. Oxidized low-density lipoproteins (oxLDLs) are found abundantly in atherosclerotic plaques. We aimed at evaluating the effects of oxLDLs on TF expression in T cells and the role of the lectin-like oxidized low-density lipoprotein receptor-1 (LOX-1). Methods and results CD3+ cells were isolated from healthy volunteers. Gene, protein, and surface expression of TF, as well as of LOX-1, were assessed at different time-points after oxLDL stimulation. To determine whether oxLDL-induced TF was LOX-1 dependent, T cells were pre-incubated with an LOX-1 inhibiting peptide (L-RBP) or with an anti-LOX-1 blocking antibody. To exclude that TF expression was mediated by reactive oxygen species (ROS) generation, oxLDL-stimulated T cells were pre-incubated with superoxide dismutase + catalase or with 4-Hydroxy-2,2,6,6-tetramethylpiperidine-1-oxyl (Tempol), an intracellular free radical scavenger. Finally, to determine if the observed findings in vitro may have a biological relevance, the presence of CD3+/TF+/LOX-1+ cells was evaluated by immunofluorescence in human carotid atherosclerotic lesions. oxLDLs induced functionally active TF expression in T cells in a dose- and time-dependent manner, independently on ROS generation. No effect was observed in native LDL-treated T cells. LOX-1 expression was also induced by oxLDLs in a time- and dose-dependent manner. Pre-incubation with L-RBP or anti-LOX-1 antibody almost completely inhibited oxLDL-mediated TF expression. Interestingly, human carotid plaques showed significant infiltration of CD3+ cells (mainly CD8+ cells), some of which were positive for both TF and LOX-1. Conclusion oxLDLs induce functional TF expression in T-lymphocytes in vitro via interaction of oxLDLs with LOX-1. Human carotid atherosclerotic plaques contain CD3+/CD8+cells that express both TF and LOX-1, indicating that also in patients these mechanisms may play an important role. Graphical Abstract Graphical Abstract</description><identifier>ISSN: 0008-6363</identifier><identifier>EISSN: 1755-3245</identifier><identifier>DOI: 10.1093/cvr/cvz230</identifier><identifier>PMID: 31504248</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Carotid Artery Diseases - genetics ; Carotid Artery Diseases - metabolism ; Carotid Artery Diseases - pathology ; Cells, Cultured ; Humans ; Lipoproteins, LDL - pharmacology ; NADPH Oxidases - metabolism ; NF-kappa B - metabolism ; Plaque, Atherosclerotic ; Reactive Oxygen Species - metabolism ; Scavenger Receptors, Class E - agonists ; Scavenger Receptors, Class E - genetics ; Scavenger Receptors, Class E - metabolism ; T-Lymphocytes - drug effects ; T-Lymphocytes - metabolism ; Thromboplastin - genetics ; Thromboplastin - metabolism ; Up-Regulation</subject><ispartof>Cardiovascular research, 2020-05, Vol.116 (6), p.1125-1135</ispartof><rights>Published on behalf of the European Society of Cardiology. All rights reserved. © The Author(s) 2019. For permissions, please email: journals.permissions@oup.com. 2019</rights><rights>Published on behalf of the European Society of Cardiology. All rights reserved. © The Author(s) 2019. For permissions, please email: journals.permissions@oup.com.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c283t-494a9f009edf6fb2bf69c91b8381f4b3d6b56547fdacc89728b2d403fc6d71603</citedby><cites>FETCH-LOGICAL-c283t-494a9f009edf6fb2bf69c91b8381f4b3d6b56547fdacc89728b2d403fc6d71603</cites><orcidid>0000-0003-2395-6710 ; 0000-0002-3590-6983</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,1584,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31504248$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cimmino, Giovanni</creatorcontrib><creatorcontrib>Cirillo, Plinio</creatorcontrib><creatorcontrib>Conte, Stefano</creatorcontrib><creatorcontrib>Pellegrino, Grazia</creatorcontrib><creatorcontrib>Barra, Giusi</creatorcontrib><creatorcontrib>Maresca, Lucio</creatorcontrib><creatorcontrib>Morello, Andrea</creatorcontrib><creatorcontrib>Calì, Gaetano</creatorcontrib><creatorcontrib>Loffredo, Francesco</creatorcontrib><creatorcontrib>De Palma, Raffaele</creatorcontrib><creatorcontrib>Arena, Giulia</creatorcontrib><creatorcontrib>Sawamura, Tatsuya</creatorcontrib><creatorcontrib>Ambrosio, Giuseppe</creatorcontrib><creatorcontrib>Golino, Paolo</creatorcontrib><title>Oxidized low-density lipoproteins induce tissue factor expression in T-lymphocytes via activation of lectin-like oxidized low-density lipoprotein receptor-1</title><title>Cardiovascular research</title><addtitle>Cardiovasc Res</addtitle><description>Abstract Aims T-lymphocytes plays an important role in the pathophysiology of acute coronary syndromes. T-cell activation in vitro by pro-inflammatory cytokines may lead to functional tissue factor (TF) expression, indicating a possible contribution of immunity to thrombosis. Oxidized low-density lipoproteins (oxLDLs) are found abundantly in atherosclerotic plaques. We aimed at evaluating the effects of oxLDLs on TF expression in T cells and the role of the lectin-like oxidized low-density lipoprotein receptor-1 (LOX-1). Methods and results CD3+ cells were isolated from healthy volunteers. Gene, protein, and surface expression of TF, as well as of LOX-1, were assessed at different time-points after oxLDL stimulation. To determine whether oxLDL-induced TF was LOX-1 dependent, T cells were pre-incubated with an LOX-1 inhibiting peptide (L-RBP) or with an anti-LOX-1 blocking antibody. To exclude that TF expression was mediated by reactive oxygen species (ROS) generation, oxLDL-stimulated T cells were pre-incubated with superoxide dismutase + catalase or with 4-Hydroxy-2,2,6,6-tetramethylpiperidine-1-oxyl (Tempol), an intracellular free radical scavenger. Finally, to determine if the observed findings in vitro may have a biological relevance, the presence of CD3+/TF+/LOX-1+ cells was evaluated by immunofluorescence in human carotid atherosclerotic lesions. oxLDLs induced functionally active TF expression in T cells in a dose- and time-dependent manner, independently on ROS generation. No effect was observed in native LDL-treated T cells. LOX-1 expression was also induced by oxLDLs in a time- and dose-dependent manner. Pre-incubation with L-RBP or anti-LOX-1 antibody almost completely inhibited oxLDL-mediated TF expression. Interestingly, human carotid plaques showed significant infiltration of CD3+ cells (mainly CD8+ cells), some of which were positive for both TF and LOX-1. Conclusion oxLDLs induce functional TF expression in T-lymphocytes in vitro via interaction of oxLDLs with LOX-1. Human carotid atherosclerotic plaques contain CD3+/CD8+cells that express both TF and LOX-1, indicating that also in patients these mechanisms may play an important role. Graphical Abstract Graphical Abstract</description><subject>Carotid Artery Diseases - genetics</subject><subject>Carotid Artery Diseases - metabolism</subject><subject>Carotid Artery Diseases - pathology</subject><subject>Cells, Cultured</subject><subject>Humans</subject><subject>Lipoproteins, LDL - pharmacology</subject><subject>NADPH Oxidases - metabolism</subject><subject>NF-kappa B - metabolism</subject><subject>Plaque, Atherosclerotic</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>Scavenger Receptors, Class E - agonists</subject><subject>Scavenger Receptors, Class E - genetics</subject><subject>Scavenger Receptors, Class E - metabolism</subject><subject>T-Lymphocytes - drug effects</subject><subject>T-Lymphocytes - metabolism</subject><subject>Thromboplastin - genetics</subject><subject>Thromboplastin - metabolism</subject><subject>Up-Regulation</subject><issn>0008-6363</issn><issn>1755-3245</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1LxDAQhoMoun5c_AGSiyBCNF9t06MsfoGwl_Vc2mSC0W5Tk3Z1_S3-WLOsetTDMAzvwzvDvAgdM3rBaCku9TKk-uCCbqEJK7KMCC6zbTShlCqSi1zsof0Yn9OYZYXcRXuCZVRyqSboc_bujPsAg1v_Rgx00Q0r3Lre98EP4LqIXWdGDXhwMY6Aba0HHzC89wFidL5LOp6TdrXon7xeDRDx0tU4UW5ZD2vdW9xCGjvSuhfA_p-FOICGPu0g7BDt2LqNcPTdD9DjzfV8ekceZrf306sHorkSA5GlrEtLaQnG5rbhjc1LXbJGCcWsbITJmyzPZGFNrbUqC64abiQVVuemYDkVB-hs45tOeB0hDtXCRQ1tW3fgx1hxrlTBOadr9HyD6uBjDGCrPrhFHVYVo9U6jSqlUW3SSPDJt-_YLMD8oj_vT8DpBvBj_5fRF1j1mEA</recordid><startdate>20200501</startdate><enddate>20200501</enddate><creator>Cimmino, Giovanni</creator><creator>Cirillo, Plinio</creator><creator>Conte, Stefano</creator><creator>Pellegrino, Grazia</creator><creator>Barra, Giusi</creator><creator>Maresca, Lucio</creator><creator>Morello, Andrea</creator><creator>Calì, Gaetano</creator><creator>Loffredo, Francesco</creator><creator>De Palma, Raffaele</creator><creator>Arena, Giulia</creator><creator>Sawamura, Tatsuya</creator><creator>Ambrosio, Giuseppe</creator><creator>Golino, Paolo</creator><general>Oxford University Press</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><orcidid>https://orcid.org/0000-0003-2395-6710</orcidid><orcidid>https://orcid.org/0000-0002-3590-6983</orcidid></search><sort><creationdate>20200501</creationdate><title>Oxidized low-density lipoproteins induce tissue factor expression in T-lymphocytes via activation of lectin-like oxidized low-density lipoprotein receptor-1</title><author>Cimmino, Giovanni ; Cirillo, Plinio ; Conte, Stefano ; Pellegrino, Grazia ; Barra, Giusi ; Maresca, Lucio ; Morello, Andrea ; Calì, Gaetano ; Loffredo, Francesco ; De Palma, Raffaele ; Arena, Giulia ; Sawamura, Tatsuya ; Ambrosio, Giuseppe ; Golino, Paolo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c283t-494a9f009edf6fb2bf69c91b8381f4b3d6b56547fdacc89728b2d403fc6d71603</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Carotid Artery Diseases - genetics</topic><topic>Carotid Artery Diseases - metabolism</topic><topic>Carotid Artery Diseases - pathology</topic><topic>Cells, Cultured</topic><topic>Humans</topic><topic>Lipoproteins, LDL - pharmacology</topic><topic>NADPH Oxidases - metabolism</topic><topic>NF-kappa B - metabolism</topic><topic>Plaque, Atherosclerotic</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>Scavenger Receptors, Class E - agonists</topic><topic>Scavenger Receptors, Class E - genetics</topic><topic>Scavenger Receptors, Class E - metabolism</topic><topic>T-Lymphocytes - drug effects</topic><topic>T-Lymphocytes - metabolism</topic><topic>Thromboplastin - genetics</topic><topic>Thromboplastin - metabolism</topic><topic>Up-Regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cimmino, Giovanni</creatorcontrib><creatorcontrib>Cirillo, Plinio</creatorcontrib><creatorcontrib>Conte, Stefano</creatorcontrib><creatorcontrib>Pellegrino, Grazia</creatorcontrib><creatorcontrib>Barra, Giusi</creatorcontrib><creatorcontrib>Maresca, Lucio</creatorcontrib><creatorcontrib>Morello, Andrea</creatorcontrib><creatorcontrib>Calì, Gaetano</creatorcontrib><creatorcontrib>Loffredo, Francesco</creatorcontrib><creatorcontrib>De Palma, Raffaele</creatorcontrib><creatorcontrib>Arena, Giulia</creatorcontrib><creatorcontrib>Sawamura, Tatsuya</creatorcontrib><creatorcontrib>Ambrosio, Giuseppe</creatorcontrib><creatorcontrib>Golino, Paolo</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><jtitle>Cardiovascular research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cimmino, Giovanni</au><au>Cirillo, Plinio</au><au>Conte, Stefano</au><au>Pellegrino, Grazia</au><au>Barra, Giusi</au><au>Maresca, Lucio</au><au>Morello, Andrea</au><au>Calì, Gaetano</au><au>Loffredo, Francesco</au><au>De Palma, Raffaele</au><au>Arena, Giulia</au><au>Sawamura, Tatsuya</au><au>Ambrosio, Giuseppe</au><au>Golino, Paolo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Oxidized low-density lipoproteins induce tissue factor expression in T-lymphocytes via activation of lectin-like oxidized low-density lipoprotein receptor-1</atitle><jtitle>Cardiovascular research</jtitle><addtitle>Cardiovasc Res</addtitle><date>2020-05-01</date><risdate>2020</risdate><volume>116</volume><issue>6</issue><spage>1125</spage><epage>1135</epage><pages>1125-1135</pages><issn>0008-6363</issn><eissn>1755-3245</eissn><abstract>Abstract Aims T-lymphocytes plays an important role in the pathophysiology of acute coronary syndromes. T-cell activation in vitro by pro-inflammatory cytokines may lead to functional tissue factor (TF) expression, indicating a possible contribution of immunity to thrombosis. Oxidized low-density lipoproteins (oxLDLs) are found abundantly in atherosclerotic plaques. We aimed at evaluating the effects of oxLDLs on TF expression in T cells and the role of the lectin-like oxidized low-density lipoprotein receptor-1 (LOX-1). Methods and results CD3+ cells were isolated from healthy volunteers. Gene, protein, and surface expression of TF, as well as of LOX-1, were assessed at different time-points after oxLDL stimulation. To determine whether oxLDL-induced TF was LOX-1 dependent, T cells were pre-incubated with an LOX-1 inhibiting peptide (L-RBP) or with an anti-LOX-1 blocking antibody. To exclude that TF expression was mediated by reactive oxygen species (ROS) generation, oxLDL-stimulated T cells were pre-incubated with superoxide dismutase + catalase or with 4-Hydroxy-2,2,6,6-tetramethylpiperidine-1-oxyl (Tempol), an intracellular free radical scavenger. Finally, to determine if the observed findings in vitro may have a biological relevance, the presence of CD3+/TF+/LOX-1+ cells was evaluated by immunofluorescence in human carotid atherosclerotic lesions. oxLDLs induced functionally active TF expression in T cells in a dose- and time-dependent manner, independently on ROS generation. No effect was observed in native LDL-treated T cells. LOX-1 expression was also induced by oxLDLs in a time- and dose-dependent manner. Pre-incubation with L-RBP or anti-LOX-1 antibody almost completely inhibited oxLDL-mediated TF expression. Interestingly, human carotid plaques showed significant infiltration of CD3+ cells (mainly CD8+ cells), some of which were positive for both TF and LOX-1. Conclusion oxLDLs induce functional TF expression in T-lymphocytes in vitro via interaction of oxLDLs with LOX-1. Human carotid atherosclerotic plaques contain CD3+/CD8+cells that express both TF and LOX-1, indicating that also in patients these mechanisms may play an important role. Graphical Abstract Graphical Abstract</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>31504248</pmid><doi>10.1093/cvr/cvz230</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0003-2395-6710</orcidid><orcidid>https://orcid.org/0000-0002-3590-6983</orcidid><oa>free_for_read</oa></addata></record>
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source MEDLINE; Oxford University Press Journals All Titles (1996-Current); EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
subjects Carotid Artery Diseases - genetics
Carotid Artery Diseases - metabolism
Carotid Artery Diseases - pathology
Cells, Cultured
Humans
Lipoproteins, LDL - pharmacology
NADPH Oxidases - metabolism
NF-kappa B - metabolism
Plaque, Atherosclerotic
Reactive Oxygen Species - metabolism
Scavenger Receptors, Class E - agonists
Scavenger Receptors, Class E - genetics
Scavenger Receptors, Class E - metabolism
T-Lymphocytes - drug effects
T-Lymphocytes - metabolism
Thromboplastin - genetics
Thromboplastin - metabolism
Up-Regulation
title Oxidized low-density lipoproteins induce tissue factor expression in T-lymphocytes via activation of lectin-like oxidized low-density lipoprotein receptor-1
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