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Influence of interleukin-1 beta gene polymorphisms on the risk of myocardial infarction and ischemic stroke at young age in vivo and in vitro

In this study, by using vivo and vitro model, we assessed whether interleukin (IL)-1beta gene polymorphisms influence on the risk of myocardial infarction and ischemic stroke at young age. 147 patients (age < 45 years) with a first episode of MI and 56 patients (age < 45 years) with first-ever...

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Published in:International journal of clinical and experimental pathology 2015-01, Vol.8 (11), p.13806-13813
Main Authors: Yang, Bo, Zhao, Hua, X, Bin, Wang, Ya-Bin, Zhang, Jian, Cao, Yu-Kang, Wu, Qing, Cao, Feng
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container_issue 11
container_start_page 13806
container_title International journal of clinical and experimental pathology
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creator Yang, Bo
Zhao, Hua
X, Bin
Wang, Ya-Bin
Zhang, Jian
Cao, Yu-Kang
Wu, Qing
Cao, Feng
description In this study, by using vivo and vitro model, we assessed whether interleukin (IL)-1beta gene polymorphisms influence on the risk of myocardial infarction and ischemic stroke at young age. 147 patients (age < 45 years) with a first episode of MI and 56 patients (age < 45 years) with first-ever cerebral ischemia consecutively were admitted to this study from the Department of Chinese PLA General Hospital. Meanwhile, 91 normal volunteers without MI or stroke were deeded as control group and greed to give blood samples for DNA analysis and biochemical measurements by written informed consent. IL-1β-511 wild type (WT, CC) and SNP (TT) were established and transfected into Rat myocardial H9c2 cell and Mouse brain endothelial bEND.3 cells. In Young Age MI or stroke patients, the IL-1β levels of patients with 511CC are higher than that of patients with 511TT. In our study, NF-κB miRNA, iNOS activity, NF-κB, iNOS and Bax protein expressions of MI-induced H9c2 cell or stroke-induced bEND.3 cells in IL-1β-511TT group were lower than those of IL-1β-511CC. Additionally, the protein expression of MMP-2 of MI-induced H9c2 cell or stroke-induced bEND.3 cells in IL-1β-511TT group were higher than that of IL-1β 511CC group. In conclusion, our data indicate that IL-1β-511TT/CC influence on the risk of myocardial infarction and ischemic stroke at young age through NF-κB, iNOS, MMP-2 and Bax.
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Meanwhile, 91 normal volunteers without MI or stroke were deeded as control group and greed to give blood samples for DNA analysis and biochemical measurements by written informed consent. IL-1β-511 wild type (WT, CC) and SNP (TT) were established and transfected into Rat myocardial H9c2 cell and Mouse brain endothelial bEND.3 cells. In Young Age MI or stroke patients, the IL-1β levels of patients with 511CC are higher than that of patients with 511TT. In our study, NF-κB miRNA, iNOS activity, NF-κB, iNOS and Bax protein expressions of MI-induced H9c2 cell or stroke-induced bEND.3 cells in IL-1β-511TT group were lower than those of IL-1β-511CC. Additionally, the protein expression of MMP-2 of MI-induced H9c2 cell or stroke-induced bEND.3 cells in IL-1β-511TT group were higher than that of IL-1β 511CC group. In conclusion, our data indicate that IL-1β-511TT/CC influence on the risk of myocardial infarction and ischemic stroke at young age through NF-κB, iNOS, MMP-2 and Bax.</description><identifier>EISSN: 1936-2625</identifier><identifier>PMID: 26823694</identifier><language>eng</language><publisher>United States: e-Century Publishing Corporation</publisher><subject>Adult ; Age of Onset ; Animals ; bcl-2-Associated X Protein - metabolism ; Brain Ischemia - diagnosis ; Brain Ischemia - genetics ; Brain Ischemia - metabolism ; Case-Control Studies ; Cell Line ; Endothelial Cells - metabolism ; Female ; Genetic Association Studies ; Genetic Predisposition to Disease ; Heterozygote ; Homozygote ; Humans ; Interleukin-1beta - genetics ; Interleukin-1beta - metabolism ; Male ; Matrix Metalloproteinase 2 - metabolism ; Mice ; Myocardial Infarction - diagnosis ; Myocardial Infarction - genetics ; Myocardial Infarction - metabolism ; NF-kappa B - genetics ; NF-kappa B - metabolism ; Nitric Oxide Synthase Type II - genetics ; Nitric Oxide Synthase Type II - metabolism ; Original ; Phenotype ; Polymorphism, Single Nucleotide ; Rats ; Risk Factors ; Stroke - diagnosis ; Stroke - genetics ; Stroke - metabolism ; Transfection</subject><ispartof>International journal of clinical and experimental pathology, 2015-01, Vol.8 (11), p.13806-13813</ispartof><rights>IJCEP Copyright © 2015 2015</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4713480/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4713480/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26823694$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yang, Bo</creatorcontrib><creatorcontrib>Zhao, Hua</creatorcontrib><creatorcontrib>X, Bin</creatorcontrib><creatorcontrib>Wang, Ya-Bin</creatorcontrib><creatorcontrib>Zhang, Jian</creatorcontrib><creatorcontrib>Cao, Yu-Kang</creatorcontrib><creatorcontrib>Wu, Qing</creatorcontrib><creatorcontrib>Cao, Feng</creatorcontrib><title>Influence of interleukin-1 beta gene polymorphisms on the risk of myocardial infarction and ischemic stroke at young age in vivo and in vitro</title><title>International journal of clinical and experimental pathology</title><addtitle>Int J Clin Exp Pathol</addtitle><description>In this study, by using vivo and vitro model, we assessed whether interleukin (IL)-1beta gene polymorphisms influence on the risk of myocardial infarction and ischemic stroke at young age. 147 patients (age &lt; 45 years) with a first episode of MI and 56 patients (age &lt; 45 years) with first-ever cerebral ischemia consecutively were admitted to this study from the Department of Chinese PLA General Hospital. Meanwhile, 91 normal volunteers without MI or stroke were deeded as control group and greed to give blood samples for DNA analysis and biochemical measurements by written informed consent. IL-1β-511 wild type (WT, CC) and SNP (TT) were established and transfected into Rat myocardial H9c2 cell and Mouse brain endothelial bEND.3 cells. In Young Age MI or stroke patients, the IL-1β levels of patients with 511CC are higher than that of patients with 511TT. In our study, NF-κB miRNA, iNOS activity, NF-κB, iNOS and Bax protein expressions of MI-induced H9c2 cell or stroke-induced bEND.3 cells in IL-1β-511TT group were lower than those of IL-1β-511CC. Additionally, the protein expression of MMP-2 of MI-induced H9c2 cell or stroke-induced bEND.3 cells in IL-1β-511TT group were higher than that of IL-1β 511CC group. In conclusion, our data indicate that IL-1β-511TT/CC influence on the risk of myocardial infarction and ischemic stroke at young age through NF-κB, iNOS, MMP-2 and Bax.</description><subject>Adult</subject><subject>Age of Onset</subject><subject>Animals</subject><subject>bcl-2-Associated X Protein - metabolism</subject><subject>Brain Ischemia - diagnosis</subject><subject>Brain Ischemia - genetics</subject><subject>Brain Ischemia - metabolism</subject><subject>Case-Control Studies</subject><subject>Cell Line</subject><subject>Endothelial Cells - metabolism</subject><subject>Female</subject><subject>Genetic Association Studies</subject><subject>Genetic Predisposition to Disease</subject><subject>Heterozygote</subject><subject>Homozygote</subject><subject>Humans</subject><subject>Interleukin-1beta - genetics</subject><subject>Interleukin-1beta - metabolism</subject><subject>Male</subject><subject>Matrix Metalloproteinase 2 - metabolism</subject><subject>Mice</subject><subject>Myocardial Infarction - diagnosis</subject><subject>Myocardial Infarction - genetics</subject><subject>Myocardial Infarction - metabolism</subject><subject>NF-kappa B - genetics</subject><subject>NF-kappa B - metabolism</subject><subject>Nitric Oxide Synthase Type II - genetics</subject><subject>Nitric Oxide Synthase Type II - metabolism</subject><subject>Original</subject><subject>Phenotype</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Rats</subject><subject>Risk Factors</subject><subject>Stroke - diagnosis</subject><subject>Stroke - genetics</subject><subject>Stroke - metabolism</subject><subject>Transfection</subject><issn>1936-2625</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNpVkc1KxDAUhYsgzjj6CpKlm0KapGlnI8jgz8CAG12XNLlt47RJTdKBPoTvbGRG0dW9cL5zDpd7liyzNeUp4SRfJJfev2PMM8LwRbIgvCSUr9ky-dyapp_ASEC2QdoEcD1Me23SDNUQBGrBABptPw_WjZ32g0fWoNABctrvv03DbKVwSos--hvhZNCREEYh7WUHg5bIB2f3gERAs51Mi0QLkUUHfbBH8HuPzFVy3ojew_VprpK3x4fXzXO6e3nabu536Ug4D2mWKUXWNcM8pwUtBTBKQNJGKiF4rRqFGaYyx02dK1rTKJUqxxllTNaEyIaukrtj7jjVAygJJjjRV6PTg3BzZYWu_itGd1VrDxUrYkqJY8DtKcDZjwl8qIZ4LPS9MGAnX2UFzxjnxZpH9OZv12_Jzw_oFzT2hlw</recordid><startdate>20150101</startdate><enddate>20150101</enddate><creator>Yang, Bo</creator><creator>Zhao, Hua</creator><creator>X, Bin</creator><creator>Wang, Ya-Bin</creator><creator>Zhang, Jian</creator><creator>Cao, Yu-Kang</creator><creator>Wu, Qing</creator><creator>Cao, Feng</creator><general>e-Century Publishing Corporation</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20150101</creationdate><title>Influence of interleukin-1 beta gene polymorphisms on the risk of myocardial infarction and ischemic stroke at young age in vivo and in vitro</title><author>Yang, Bo ; 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45 years) with a first episode of MI and 56 patients (age &lt; 45 years) with first-ever cerebral ischemia consecutively were admitted to this study from the Department of Chinese PLA General Hospital. Meanwhile, 91 normal volunteers without MI or stroke were deeded as control group and greed to give blood samples for DNA analysis and biochemical measurements by written informed consent. IL-1β-511 wild type (WT, CC) and SNP (TT) were established and transfected into Rat myocardial H9c2 cell and Mouse brain endothelial bEND.3 cells. In Young Age MI or stroke patients, the IL-1β levels of patients with 511CC are higher than that of patients with 511TT. In our study, NF-κB miRNA, iNOS activity, NF-κB, iNOS and Bax protein expressions of MI-induced H9c2 cell or stroke-induced bEND.3 cells in IL-1β-511TT group were lower than those of IL-1β-511CC. Additionally, the protein expression of MMP-2 of MI-induced H9c2 cell or stroke-induced bEND.3 cells in IL-1β-511TT group were higher than that of IL-1β 511CC group. In conclusion, our data indicate that IL-1β-511TT/CC influence on the risk of myocardial infarction and ischemic stroke at young age through NF-κB, iNOS, MMP-2 and Bax.</abstract><cop>United States</cop><pub>e-Century Publishing Corporation</pub><pmid>26823694</pmid><tpages>8</tpages></addata></record>
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ispartof International journal of clinical and experimental pathology, 2015-01, Vol.8 (11), p.13806-13813
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language eng
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source PubMed Central
subjects Adult
Age of Onset
Animals
bcl-2-Associated X Protein - metabolism
Brain Ischemia - diagnosis
Brain Ischemia - genetics
Brain Ischemia - metabolism
Case-Control Studies
Cell Line
Endothelial Cells - metabolism
Female
Genetic Association Studies
Genetic Predisposition to Disease
Heterozygote
Homozygote
Humans
Interleukin-1beta - genetics
Interleukin-1beta - metabolism
Male
Matrix Metalloproteinase 2 - metabolism
Mice
Myocardial Infarction - diagnosis
Myocardial Infarction - genetics
Myocardial Infarction - metabolism
NF-kappa B - genetics
NF-kappa B - metabolism
Nitric Oxide Synthase Type II - genetics
Nitric Oxide Synthase Type II - metabolism
Original
Phenotype
Polymorphism, Single Nucleotide
Rats
Risk Factors
Stroke - diagnosis
Stroke - genetics
Stroke - metabolism
Transfection
title Influence of interleukin-1 beta gene polymorphisms on the risk of myocardial infarction and ischemic stroke at young age in vivo and in vitro
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