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ST2L Transmembrane Receptor Expression: An Immunochemical Study on Endarterectomy Samples
ST2 (suppression of tumorigenity) has been described as a receptor for the interleukin-33, a member of the IL-1 family of cytokines. It is associated to coronary artery disease, all-causes mortality and cardiovascular mortality. The present study was designed to assess the immunohistochemical expres...
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Published in: | PloS one 2016-05, Vol.11 (5), p.e0156315-e0156315 |
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description | ST2 (suppression of tumorigenity) has been described as a receptor for the interleukin-33, a member of the IL-1 family of cytokines. It is associated to coronary artery disease, all-causes mortality and cardiovascular mortality.
The present study was designed to assess the immunohistochemical expression of the ST2 receptor (ST2L/Il-1R) in atherosclerotic plaques of formalin fixed paraffin-embedded internal carotid arteries of patients with and without cerebro-vascular symptoms.
The study involved 41 cases (23 asymptomatic and 18 symptomatic). All the clinical and morphological parameters examined were uniformly distributed between the two groups, with a mild predominance of degree of calcification in asymptomatic cases (p = 0.01). ST2L expression was found to be more evident as a membrane pattern in macrophages when observing carotid atherosclerotic plaques of symptomatic patients, rather than in asymptomatic patients' plaques (77.7% vs 39.1%; p = 0.015), and its expression was particularly remarkable in VI type plaque (AHA). Significantly, ST2L was marked by the endothelium of neoangiogenetic vessels on the shoulder region of the plaque, but not (apart from a few cases) in the endothelium covering the residual lumen of the vessel.
The ST2L immunohistochemical expression was for the first time investigated in a large number of human carotid atherosclerotic plaques, as for its pattern of distribution in the different plaque cell populations. Furthermore, ST2L was particularly remarkable on macrophages, as a membrane pattern, of symptomatic patients' plaque. Considering our data, we hypothesize that ST2L/IL33 axis could drive the mechanism of plaque development and eventually rupture. |
doi_str_mv | 10.1371/journal.pone.0156315 |
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The present study was designed to assess the immunohistochemical expression of the ST2 receptor (ST2L/Il-1R) in atherosclerotic plaques of formalin fixed paraffin-embedded internal carotid arteries of patients with and without cerebro-vascular symptoms.
The study involved 41 cases (23 asymptomatic and 18 symptomatic). All the clinical and morphological parameters examined were uniformly distributed between the two groups, with a mild predominance of degree of calcification in asymptomatic cases (p = 0.01). ST2L expression was found to be more evident as a membrane pattern in macrophages when observing carotid atherosclerotic plaques of symptomatic patients, rather than in asymptomatic patients' plaques (77.7% vs 39.1%; p = 0.015), and its expression was particularly remarkable in VI type plaque (AHA). Significantly, ST2L was marked by the endothelium of neoangiogenetic vessels on the shoulder region of the plaque, but not (apart from a few cases) in the endothelium covering the residual lumen of the vessel.
The ST2L immunohistochemical expression was for the first time investigated in a large number of human carotid atherosclerotic plaques, as for its pattern of distribution in the different plaque cell populations. Furthermore, ST2L was particularly remarkable on macrophages, as a membrane pattern, of symptomatic patients' plaque. Considering our data, we hypothesize that ST2L/IL33 axis could drive the mechanism of plaque development and eventually rupture.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0156315</identifier><identifier>PMID: 27223112</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Arteries ; Arteriosclerosis ; Arthritis ; Atherosclerosis ; Biology and Life Sciences ; Blood vessels ; Calcification ; Cardiovascular disease ; Cardiovascular diseases ; Carotid arteries ; Carotid artery ; Carotid Artery Diseases - metabolism ; Carotid Artery Diseases - surgery ; Cell adhesion & migration ; Cell Membrane - metabolism ; Coronary artery ; Coronary artery disease ; Coronary heart disease ; Coronary vessels ; Cytokines ; Development and progression ; Endarterectomy, Carotid ; Endothelium ; Female ; Gene expression ; Genetic aspects ; Heart ; Heart diseases ; Humans ; Interleukin 1 ; Interleukin 1 receptors ; Interleukin-1 Receptor-Like 1 Protein - metabolism ; Interleukin-33 - metabolism ; Ischemia ; Kinases ; Macrophages ; Macrophages - metabolism ; Male ; Medical schools ; Medicine and Health Sciences ; Membrane proteins ; Middle Aged ; Mortality ; Paraffin ; Patients ; Physiological aspects ; Plaque, Atherosclerotic - metabolism ; Plaque, Atherosclerotic - surgery ; Plaques ; Risk factors ; Vascular surgery</subject><ispartof>PloS one, 2016-05, Vol.11 (5), p.e0156315-e0156315</ispartof><rights>COPYRIGHT 2016 Public Library of Science</rights><rights>2016 Marzullo et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2016 Marzullo et al 2016 Marzullo et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-64fa1b56712d4bd9c169efdd2a7d6d8b64ac2ca970da3d025a4148ad61b849e73</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1791324545/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1791324545?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,74998</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27223112$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Dileepan, Kottarappat N</contributor><creatorcontrib>Marzullo, Andrea</creatorcontrib><creatorcontrib>Ambrosi, Francesca</creatorcontrib><creatorcontrib>Inchingolo, Mirjam</creatorcontrib><creatorcontrib>Manca, Fabio</creatorcontrib><creatorcontrib>Devito, Fiorella</creatorcontrib><creatorcontrib>Angiletta, Domenico</creatorcontrib><creatorcontrib>Zito, Annapaola</creatorcontrib><creatorcontrib>Scicchitano, Pietro</creatorcontrib><creatorcontrib>Ciccone, Marco Matteo</creatorcontrib><title>ST2L Transmembrane Receptor Expression: An Immunochemical Study on Endarterectomy Samples</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>ST2 (suppression of tumorigenity) has been described as a receptor for the interleukin-33, a member of the IL-1 family of cytokines. It is associated to coronary artery disease, all-causes mortality and cardiovascular mortality.
The present study was designed to assess the immunohistochemical expression of the ST2 receptor (ST2L/Il-1R) in atherosclerotic plaques of formalin fixed paraffin-embedded internal carotid arteries of patients with and without cerebro-vascular symptoms.
The study involved 41 cases (23 asymptomatic and 18 symptomatic). All the clinical and morphological parameters examined were uniformly distributed between the two groups, with a mild predominance of degree of calcification in asymptomatic cases (p = 0.01). ST2L expression was found to be more evident as a membrane pattern in macrophages when observing carotid atherosclerotic plaques of symptomatic patients, rather than in asymptomatic patients' plaques (77.7% vs 39.1%; p = 0.015), and its expression was particularly remarkable in VI type plaque (AHA). Significantly, ST2L was marked by the endothelium of neoangiogenetic vessels on the shoulder region of the plaque, but not (apart from a few cases) in the endothelium covering the residual lumen of the vessel.
The ST2L immunohistochemical expression was for the first time investigated in a large number of human carotid atherosclerotic plaques, as for its pattern of distribution in the different plaque cell populations. Furthermore, ST2L was particularly remarkable on macrophages, as a membrane pattern, of symptomatic patients' plaque. Considering our data, we hypothesize that ST2L/IL33 axis could drive the mechanism of plaque development and eventually rupture.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Arteries</subject><subject>Arteriosclerosis</subject><subject>Arthritis</subject><subject>Atherosclerosis</subject><subject>Biology and Life Sciences</subject><subject>Blood vessels</subject><subject>Calcification</subject><subject>Cardiovascular disease</subject><subject>Cardiovascular diseases</subject><subject>Carotid arteries</subject><subject>Carotid artery</subject><subject>Carotid Artery Diseases - metabolism</subject><subject>Carotid Artery Diseases - surgery</subject><subject>Cell adhesion & migration</subject><subject>Cell Membrane - metabolism</subject><subject>Coronary artery</subject><subject>Coronary artery disease</subject><subject>Coronary heart disease</subject><subject>Coronary vessels</subject><subject>Cytokines</subject><subject>Development and progression</subject><subject>Endarterectomy, Carotid</subject><subject>Endothelium</subject><subject>Female</subject><subject>Gene expression</subject><subject>Genetic aspects</subject><subject>Heart</subject><subject>Heart diseases</subject><subject>Humans</subject><subject>Interleukin 1</subject><subject>Interleukin 1 receptors</subject><subject>Interleukin-1 Receptor-Like 1 Protein - metabolism</subject><subject>Interleukin-33 - metabolism</subject><subject>Ischemia</subject><subject>Kinases</subject><subject>Macrophages</subject><subject>Macrophages - metabolism</subject><subject>Male</subject><subject>Medical schools</subject><subject>Medicine and Health Sciences</subject><subject>Membrane proteins</subject><subject>Middle Aged</subject><subject>Mortality</subject><subject>Paraffin</subject><subject>Patients</subject><subject>Physiological aspects</subject><subject>Plaque, Atherosclerotic - metabolism</subject><subject>Plaque, Atherosclerotic - surgery</subject><subject>Plaques</subject><subject>Risk factors</subject><subject>Vascular surgery</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNk12LEzEUhgdR3A_9B6IDguhFa74mM_FCKEvVQmFhWwWvQibJtFMykzHJyPbfb7qdXTqyF5KLJCfPeXNyck6SvIFgCnEOP-9s71phpp1t9RTAjGKYPUvOIcNoQhHAz0_WZ8mF9zsAMlxQ-jI5QzlCGEJ0nvxerdEyXTvR-kY3ZZx1eqOl7oJ16fy2c9r72rZf0lmbLpqmb63c6qaWwqSr0Kt9att03irhgnZaBtvs05VoOqP9q-RFJYzXr4f5Mvn5bb6--jFZXn9fXM2WE0kZChNKKgHLjOYQKVIqJiFlulIKiVxRVZSUCImkYDlQAiuAMkEgKYSisCwI0zm-TN4ddTtjPR-y4jnMGcSIZCSLxOJIKCt2vHN1I9yeW1Hze4N1Gx7jr6XRXOBcgBwUBckRkWXJQFlkilVaMQbiPmp9HW7ry0YrqdvghBmJjk_aess39i8nRQEwBlHg4yDg7J9e-8Cb2kttTMy87e_jRrgAjOKIvv8Hffp1A7UR8QF1W9l4rzyI8lk8xhkrAInU9AkqDnX4zVhCVR3tI4dPI4fIBH0bNqL3ni9WN__PXv8asx9O2K0WJmy9NX2IVebHIDmC0lnvna4ekwwBP3TAQzb4oQP40AHR7e3pBz06PZQ8vgPHBwDc</recordid><startdate>20160525</startdate><enddate>20160525</enddate><creator>Marzullo, Andrea</creator><creator>Ambrosi, Francesca</creator><creator>Inchingolo, Mirjam</creator><creator>Manca, Fabio</creator><creator>Devito, Fiorella</creator><creator>Angiletta, Domenico</creator><creator>Zito, Annapaola</creator><creator>Scicchitano, Pietro</creator><creator>Ciccone, Marco Matteo</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20160525</creationdate><title>ST2L Transmembrane Receptor Expression: An Immunochemical Study on Endarterectomy Samples</title><author>Marzullo, Andrea ; Ambrosi, Francesca ; Inchingolo, Mirjam ; Manca, Fabio ; Devito, Fiorella ; Angiletta, Domenico ; Zito, Annapaola ; Scicchitano, Pietro ; Ciccone, Marco Matteo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-64fa1b56712d4bd9c169efdd2a7d6d8b64ac2ca970da3d025a4148ad61b849e73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Arteries</topic><topic>Arteriosclerosis</topic><topic>Arthritis</topic><topic>Atherosclerosis</topic><topic>Biology and Life Sciences</topic><topic>Blood vessels</topic><topic>Calcification</topic><topic>Cardiovascular disease</topic><topic>Cardiovascular diseases</topic><topic>Carotid arteries</topic><topic>Carotid artery</topic><topic>Carotid Artery Diseases - metabolism</topic><topic>Carotid Artery Diseases - surgery</topic><topic>Cell adhesion & migration</topic><topic>Cell Membrane - metabolism</topic><topic>Coronary artery</topic><topic>Coronary artery disease</topic><topic>Coronary heart disease</topic><topic>Coronary vessels</topic><topic>Cytokines</topic><topic>Development and progression</topic><topic>Endarterectomy, Carotid</topic><topic>Endothelium</topic><topic>Female</topic><topic>Gene expression</topic><topic>Genetic aspects</topic><topic>Heart</topic><topic>Heart diseases</topic><topic>Humans</topic><topic>Interleukin 1</topic><topic>Interleukin 1 receptors</topic><topic>Interleukin-1 Receptor-Like 1 Protein - metabolism</topic><topic>Interleukin-33 - metabolism</topic><topic>Ischemia</topic><topic>Kinases</topic><topic>Macrophages</topic><topic>Macrophages - metabolism</topic><topic>Male</topic><topic>Medical schools</topic><topic>Medicine and Health Sciences</topic><topic>Membrane proteins</topic><topic>Middle Aged</topic><topic>Mortality</topic><topic>Paraffin</topic><topic>Patients</topic><topic>Physiological aspects</topic><topic>Plaque, Atherosclerotic - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Marzullo, Andrea</au><au>Ambrosi, Francesca</au><au>Inchingolo, Mirjam</au><au>Manca, Fabio</au><au>Devito, Fiorella</au><au>Angiletta, Domenico</au><au>Zito, Annapaola</au><au>Scicchitano, Pietro</au><au>Ciccone, Marco Matteo</au><au>Dileepan, Kottarappat N</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>ST2L Transmembrane Receptor Expression: An Immunochemical Study on Endarterectomy Samples</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2016-05-25</date><risdate>2016</risdate><volume>11</volume><issue>5</issue><spage>e0156315</spage><epage>e0156315</epage><pages>e0156315-e0156315</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>ST2 (suppression of tumorigenity) has been described as a receptor for the interleukin-33, a member of the IL-1 family of cytokines. It is associated to coronary artery disease, all-causes mortality and cardiovascular mortality.
The present study was designed to assess the immunohistochemical expression of the ST2 receptor (ST2L/Il-1R) in atherosclerotic plaques of formalin fixed paraffin-embedded internal carotid arteries of patients with and without cerebro-vascular symptoms.
The study involved 41 cases (23 asymptomatic and 18 symptomatic). All the clinical and morphological parameters examined were uniformly distributed between the two groups, with a mild predominance of degree of calcification in asymptomatic cases (p = 0.01). ST2L expression was found to be more evident as a membrane pattern in macrophages when observing carotid atherosclerotic plaques of symptomatic patients, rather than in asymptomatic patients' plaques (77.7% vs 39.1%; p = 0.015), and its expression was particularly remarkable in VI type plaque (AHA). Significantly, ST2L was marked by the endothelium of neoangiogenetic vessels on the shoulder region of the plaque, but not (apart from a few cases) in the endothelium covering the residual lumen of the vessel.
The ST2L immunohistochemical expression was for the first time investigated in a large number of human carotid atherosclerotic plaques, as for its pattern of distribution in the different plaque cell populations. Furthermore, ST2L was particularly remarkable on macrophages, as a membrane pattern, of symptomatic patients' plaque. Considering our data, we hypothesize that ST2L/IL33 axis could drive the mechanism of plaque development and eventually rupture.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>27223112</pmid><doi>10.1371/journal.pone.0156315</doi><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Aged, 80 and over Arteries Arteriosclerosis Arthritis Atherosclerosis Biology and Life Sciences Blood vessels Calcification Cardiovascular disease Cardiovascular diseases Carotid arteries Carotid artery Carotid Artery Diseases - metabolism Carotid Artery Diseases - surgery Cell adhesion & migration Cell Membrane - metabolism Coronary artery Coronary artery disease Coronary heart disease Coronary vessels Cytokines Development and progression Endarterectomy, Carotid Endothelium Female Gene expression Genetic aspects Heart Heart diseases Humans Interleukin 1 Interleukin 1 receptors Interleukin-1 Receptor-Like 1 Protein - metabolism Interleukin-33 - metabolism Ischemia Kinases Macrophages Macrophages - metabolism Male Medical schools Medicine and Health Sciences Membrane proteins Middle Aged Mortality Paraffin Patients Physiological aspects Plaque, Atherosclerotic - metabolism Plaque, Atherosclerotic - surgery Plaques Risk factors Vascular surgery |
title | ST2L Transmembrane Receptor Expression: An Immunochemical Study on Endarterectomy Samples |
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