Upregulation of ANGPTL4 Messenger RNA and Protein in Severely Calcified Carotid Plaques

Background In carotid atherosclerotic lesions, calcified plaques are thought to be stable and to evoke very few symptoms. However, the molecular activity in calcified plaques and their clinical significance have not been fully clarified yet. Methods Carotid plaques from 18 endarterectomy patients we...

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Veröffentlicht in:Journal of stroke and cerebrovascular diseases 2014-05, Vol.23 (5), p.933-947
Hauptverfasser: Katano, Hiroyuki, MD, PhD, Yamada, Kazuo, MD, PhD
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creator Katano, Hiroyuki, MD, PhD
Yamada, Kazuo, MD, PhD
description Background In carotid atherosclerotic lesions, calcified plaques are thought to be stable and to evoke very few symptoms. However, the molecular activity in calcified plaques and their clinical significance have not been fully clarified yet. Methods Carotid plaques from 18 endarterectomy patients were classified into high- and low-calcified plaques on the basis of Agatston calcium score. Twelve plaques were investigated for the alteration of gene expression by microarray analysis and real-time polymerase chain reaction (PCR) and 6 other plaques underwent protein assessment to elucidate the difference in molecular biological activity between the groups. Results Microarray analysis demonstrated 93 angiogenesis or growth factor–related transcripts that are reliably expressed (175 probe sets). Among them, angiopoietin-like protein 4 (ANGPTL4) expression was significantly elevated, whereas fibroblast growth factor receptor 2 (FGFR2) expression was significantly suppressed. Quantitative messenger RNA analysis was performed with real-time PCR. Augmented or decreased protein expression of each gene was confirmed by Western blotting analysis and immunohistochemistry. Conclusions In high-calcified plaques, ANGPTL4 might be upregulated for antiangiogenic modulating function together with the downregulation of FGFR2, contributing to the stability of the plaques.
doi_str_mv 10.1016/j.jstrokecerebrovasdis.2013.07.046
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However, the molecular activity in calcified plaques and their clinical significance have not been fully clarified yet. Methods Carotid plaques from 18 endarterectomy patients were classified into high- and low-calcified plaques on the basis of Agatston calcium score. Twelve plaques were investigated for the alteration of gene expression by microarray analysis and real-time polymerase chain reaction (PCR) and 6 other plaques underwent protein assessment to elucidate the difference in molecular biological activity between the groups. Results Microarray analysis demonstrated 93 angiogenesis or growth factor–related transcripts that are reliably expressed (175 probe sets). Among them, angiopoietin-like protein 4 (ANGPTL4) expression was significantly elevated, whereas fibroblast growth factor receptor 2 (FGFR2) expression was significantly suppressed. Quantitative messenger RNA analysis was performed with real-time PCR. Augmented or decreased protein expression of each gene was confirmed by Western blotting analysis and immunohistochemistry. Conclusions In high-calcified plaques, ANGPTL4 might be upregulated for antiangiogenic modulating function together with the downregulation of FGFR2, contributing to the stability of the plaques.</description><identifier>ISSN: 1052-3057</identifier><identifier>EISSN: 1532-8511</identifier><identifier>DOI: 10.1016/j.jstrokecerebrovasdis.2013.07.046</identifier><identifier>PMID: 24075588</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Aged ; angiogenesis ; Angiopoietin-like 4 Protein ; Angiopoietins - genetics ; ANGPTL4 ; Blotting, Western ; calcification ; Cardiovascular ; Carotid Artery Diseases - genetics ; Carotid Artery Diseases - pathology ; Carotid plaque ; Female ; FGFR2 ; Gene Expression Profiling - methods ; Humans ; Immunohistochemistry ; Male ; microarray analysis ; Middle Aged ; Neurology ; Oligonucleotide Array Sequence Analysis ; Plaque, Atherosclerotic ; Prognosis ; Real-Time Polymerase Chain Reaction ; Receptor, Fibroblast Growth Factor, Type 2 - genetics ; Reverse Transcriptase Polymerase Chain Reaction ; RNA, Messenger - analysis ; Severity of Illness Index ; Up-Regulation ; Vascular Calcification - genetics ; Vascular Calcification - pathology</subject><ispartof>Journal of stroke and cerebrovascular diseases, 2014-05, Vol.23 (5), p.933-947</ispartof><rights>National Stroke Association</rights><rights>2014 National Stroke Association</rights><rights>Copyright © 2014 National Stroke Association. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c459t-9ef723c9e9644b2c52c7c2d8ec76815010ba0814df9004fc49bc1cef9d0e07fd3</citedby><cites>FETCH-LOGICAL-c459t-9ef723c9e9644b2c52c7c2d8ec76815010ba0814df9004fc49bc1cef9d0e07fd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1052305713003297$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24075588$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Katano, Hiroyuki, MD, PhD</creatorcontrib><creatorcontrib>Yamada, Kazuo, MD, PhD</creatorcontrib><title>Upregulation of ANGPTL4 Messenger RNA and Protein in Severely Calcified Carotid Plaques</title><title>Journal of stroke and cerebrovascular diseases</title><addtitle>J Stroke Cerebrovasc Dis</addtitle><description>Background In carotid atherosclerotic lesions, calcified plaques are thought to be stable and to evoke very few symptoms. However, the molecular activity in calcified plaques and their clinical significance have not been fully clarified yet. Methods Carotid plaques from 18 endarterectomy patients were classified into high- and low-calcified plaques on the basis of Agatston calcium score. Twelve plaques were investigated for the alteration of gene expression by microarray analysis and real-time polymerase chain reaction (PCR) and 6 other plaques underwent protein assessment to elucidate the difference in molecular biological activity between the groups. Results Microarray analysis demonstrated 93 angiogenesis or growth factor–related transcripts that are reliably expressed (175 probe sets). Among them, angiopoietin-like protein 4 (ANGPTL4) expression was significantly elevated, whereas fibroblast growth factor receptor 2 (FGFR2) expression was significantly suppressed. Quantitative messenger RNA analysis was performed with real-time PCR. Augmented or decreased protein expression of each gene was confirmed by Western blotting analysis and immunohistochemistry. Conclusions In high-calcified plaques, ANGPTL4 might be upregulated for antiangiogenic modulating function together with the downregulation of FGFR2, contributing to the stability of the plaques.</description><subject>Aged</subject><subject>angiogenesis</subject><subject>Angiopoietin-like 4 Protein</subject><subject>Angiopoietins - genetics</subject><subject>ANGPTL4</subject><subject>Blotting, Western</subject><subject>calcification</subject><subject>Cardiovascular</subject><subject>Carotid Artery Diseases - genetics</subject><subject>Carotid Artery Diseases - pathology</subject><subject>Carotid plaque</subject><subject>Female</subject><subject>FGFR2</subject><subject>Gene Expression Profiling - methods</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Male</subject><subject>microarray analysis</subject><subject>Middle Aged</subject><subject>Neurology</subject><subject>Oligonucleotide Array Sequence Analysis</subject><subject>Plaque, Atherosclerotic</subject><subject>Prognosis</subject><subject>Real-Time Polymerase Chain Reaction</subject><subject>Receptor, Fibroblast Growth Factor, Type 2 - genetics</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>RNA, Messenger - analysis</subject><subject>Severity of Illness Index</subject><subject>Up-Regulation</subject><subject>Vascular Calcification - genetics</subject><subject>Vascular Calcification - pathology</subject><issn>1052-3057</issn><issn>1532-8511</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkU9r3DAQxU1paNK0X6H4WAp2R7JkWZfCdmnTwjYJ-UOPQpbGQY7X2kr2wn77ymzaQ-klMDADerw3-k2WfSBQEiD1x77s4xT8IxoM2Aa_19G6WFIgVQmiBFa_yM4Ir2jRcEJephk4LSrg4jR7HWMPQAhv-KvslDIQnDfNWfbzfhfwYR705PyY-y5fXV5c321Y_gNjxPEBQ35zucr1aPPr4Cd0Y57qFvdpheGQr_VgXOfQpik9u6Qa9K8Z45vspNNDxLdP_Ty7__rlbv2t2FxdfF-vNoVhXE6FxE7QykiUNWMtNZwaYaht0Ii6IRwItBoawmwnAVhnmGwNMdhJCwiis9V59v7ouwt-yZ3U1kWDw6BH9HNUhFPZMMZEnaSfj1ITfIwBO7ULbqvDQRFQC2DVq_8BVgtgBUIlwMnk3VPe3G7R_rX4QzQJNkcBpl_vHQYVjcPRoHUBzaSsd8_L-_SPnRnc6IweHvGAsfdzGBNfRVSkCtTtcvLl4qQCqKgU1W8OU69b</recordid><startdate>20140501</startdate><enddate>20140501</enddate><creator>Katano, Hiroyuki, MD, PhD</creator><creator>Yamada, Kazuo, MD, PhD</creator><general>Elsevier 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></search><sort><creationdate>20140501</creationdate><title>Upregulation of ANGPTL4 Messenger RNA and Protein in Severely Calcified Carotid Plaques</title><author>Katano, Hiroyuki, MD, PhD ; Yamada, Kazuo, MD, PhD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c459t-9ef723c9e9644b2c52c7c2d8ec76815010ba0814df9004fc49bc1cef9d0e07fd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Aged</topic><topic>angiogenesis</topic><topic>Angiopoietin-like 4 Protein</topic><topic>Angiopoietins - genetics</topic><topic>ANGPTL4</topic><topic>Blotting, Western</topic><topic>calcification</topic><topic>Cardiovascular</topic><topic>Carotid Artery Diseases - genetics</topic><topic>Carotid Artery Diseases - pathology</topic><topic>Carotid plaque</topic><topic>Female</topic><topic>FGFR2</topic><topic>Gene Expression Profiling - methods</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Male</topic><topic>microarray analysis</topic><topic>Middle Aged</topic><topic>Neurology</topic><topic>Oligonucleotide Array Sequence Analysis</topic><topic>Plaque, Atherosclerotic</topic><topic>Prognosis</topic><topic>Real-Time Polymerase Chain Reaction</topic><topic>Receptor, Fibroblast Growth Factor, Type 2 - genetics</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>RNA, Messenger - analysis</topic><topic>Severity of Illness Index</topic><topic>Up-Regulation</topic><topic>Vascular Calcification - genetics</topic><topic>Vascular Calcification - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Katano, Hiroyuki, MD, PhD</creatorcontrib><creatorcontrib>Yamada, Kazuo, MD, PhD</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>Journal of stroke and cerebrovascular diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Katano, Hiroyuki, MD, PhD</au><au>Yamada, Kazuo, MD, PhD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Upregulation of ANGPTL4 Messenger RNA and Protein in Severely Calcified Carotid Plaques</atitle><jtitle>Journal of stroke and cerebrovascular diseases</jtitle><addtitle>J Stroke Cerebrovasc Dis</addtitle><date>2014-05-01</date><risdate>2014</risdate><volume>23</volume><issue>5</issue><spage>933</spage><epage>947</epage><pages>933-947</pages><issn>1052-3057</issn><eissn>1532-8511</eissn><abstract>Background In carotid atherosclerotic lesions, calcified plaques are thought to be stable and to evoke very few symptoms. However, the molecular activity in calcified plaques and their clinical significance have not been fully clarified yet. Methods Carotid plaques from 18 endarterectomy patients were classified into high- and low-calcified plaques on the basis of Agatston calcium score. Twelve plaques were investigated for the alteration of gene expression by microarray analysis and real-time polymerase chain reaction (PCR) and 6 other plaques underwent protein assessment to elucidate the difference in molecular biological activity between the groups. Results Microarray analysis demonstrated 93 angiogenesis or growth factor–related transcripts that are reliably expressed (175 probe sets). Among them, angiopoietin-like protein 4 (ANGPTL4) expression was significantly elevated, whereas fibroblast growth factor receptor 2 (FGFR2) expression was significantly suppressed. Quantitative messenger RNA analysis was performed with real-time PCR. Augmented or decreased protein expression of each gene was confirmed by Western blotting analysis and immunohistochemistry. Conclusions In high-calcified plaques, ANGPTL4 might be upregulated for antiangiogenic modulating function together with the downregulation of FGFR2, contributing to the stability of the plaques.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>24075588</pmid><doi>10.1016/j.jstrokecerebrovasdis.2013.07.046</doi><tpages>15</tpages></addata></record>
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subjects Aged
angiogenesis
Angiopoietin-like 4 Protein
Angiopoietins - genetics
ANGPTL4
Blotting, Western
calcification
Cardiovascular
Carotid Artery Diseases - genetics
Carotid Artery Diseases - pathology
Carotid plaque
Female
FGFR2
Gene Expression Profiling - methods
Humans
Immunohistochemistry
Male
microarray analysis
Middle Aged
Neurology
Oligonucleotide Array Sequence Analysis
Plaque, Atherosclerotic
Prognosis
Real-Time Polymerase Chain Reaction
Receptor, Fibroblast Growth Factor, Type 2 - genetics
Reverse Transcriptase Polymerase Chain Reaction
RNA, Messenger - analysis
Severity of Illness Index
Up-Regulation
Vascular Calcification - genetics
Vascular Calcification - pathology
title Upregulation of ANGPTL4 Messenger RNA and Protein in Severely Calcified Carotid Plaques
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