High mobility group box 1 was associated with thrombosis in patients with atrial fibrillation

被引:14
作者
Xu, Qiwen [1 ]
Bo, Lin [1 ]
Hu, Jiaxin [2 ]
Geng, Jin [1 ]
Chen, Yuhan [2 ]
Li, Xuelin [2 ]
Chen, Fu [2 ]
Song, Jie [1 ]
机构
[1] Nanjing Med Univ, Nanjing Drum Tower Hosp, Dept Cardiol, Nanjing 210008, Jiangsu, Peoples R China
[2] Nanjing Univ, Dept Cardiol, Nanjing Drum Tower Hosp, Sch Med, Nanjing, Jiangsu, Peoples R China
关键词
atrial fibrillation; HMGB1; MyD88; TF; thrombus; HMGB PROTEINS; INFLAMMATION; ACTIVATION; PATHOGENESIS; POLYMORPHISM; INVOLVEMENT; CAVEOLIN-1; STRESS; RISK;
D O I
10.1097/MD.0000000000010132
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction:High mobility group box 1 (HMGB1) is a member of the HMGB family that is involved in inflammatory disease-related thrombosis. We hypothesize that HMGB1 and its downstream factors are associated with thrombosis in atrial fibrillation (AF).Materials and methods:Our experimental materials were the left atrial appendage (LAA) tissues from patients undergoing valve replacement. The samples were divided into 3 groups: a sinus rhythm group (n=15), an AF(+)thrombus(-)group (n=15), and an AF(+) thrombus (+)group (n=15). The expression of HMGB1, Toll-like receptor 4 (TLR4), advanced glycation end product (RAGE), myeloid differentiation factor 88 (MyD88), nuclear factor B (NFB), p-NFB, and tissue factor (TF) were detected by Western blot and immunohistochemical (IHC) staining. The expressions of interleukin-1 beta, interleukin 6, and tumor necrosis factor-alpha were detected by quantitative real-time PCR.Results:The Western blots revealed significantly higher expressions of HMGB1, MyD88, p-NFB/NFB, and TF in the AF(+)thrombus(+) group than in the other 2 groups. However, no differences in TLR4 or RAGE expression were found between the groups. IHC staining also revealed higher expressions of HMGB1 and TF in the AF(+)thrombus(+) group. The increased mRNA expressions of classic inflammatory factors (i.e., interleukin-1 beta, interleukin 6, and tumor necrosis factor-alpha) in AF(+)thrombus(+) group further validated the correlation between inflammation and thrombi in atrial fibrillation.Conclusions:HMGB1 was associated with thrombosis in patients with AF via the MyD88/NFB pathway after adjustment for cardiac and extra cardiac inflammation variables.
引用
收藏
页数:8
相关论文
共 43 条
[1]   HMGB proteins and gene expression [J].
Agresti, A ;
Bianchi, ME .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2003, 13 (02) :170-178
[2]   Acute onset human atrial fibrillation is associated with local cardiac platelet activation and endothelial dysfunction [J].
Akar, Joseph G. ;
Jeske, Walter ;
Wilber, David J. .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2008, 51 (18) :1790-1793
[3]   The role of HMGB1 in the pathogenesis of rheumatic disease [J].
Andersson, Ulf ;
Harris, Helena Erlandsson .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS, 2010, 1799 (1-2) :141-148
[4]   Inflammation as a risk factor for atrial fibrillation [J].
Aviles, RJ ;
Martin, DO ;
Apperson-Hansen, C ;
Houghtaling, PL ;
Rautaharju, P ;
Kronmal, RA ;
Tracy, RP ;
Van Wagoner, DR ;
Psaty, BM ;
Lauer, MS ;
Chung, MK .
CIRCULATION, 2003, 108 (24) :3006-3010
[5]   Chromatin unfolding and activation by HMGN chromosomal proteins [J].
Bustin, M .
TRENDS IN BIOCHEMICAL SCIENCES, 2001, 26 (07) :431-437
[6]  
Bustin M, 1999, MOL CELL BIOL, V19, P5237
[7]   Meta-analysis identifies six new susceptibility loci for atrial fibrillation [J].
Ellinor, Patrick T. ;
Lunetta, Kathryn L. ;
Albert, Christine M. ;
Glazer, Nicole L. ;
Ritchie, Marylyn D. ;
Smith, Albert V. ;
Arking, Dan E. ;
Mueller-Nurasyid, Martina ;
Krijthe, Bouwe P. ;
Lubitz, Steven A. ;
Bis, Joshua C. ;
Chung, Mina K. ;
Doerr, Marcus ;
Ozaki, Kouichi ;
Roberts, Jason D. ;
Smith, J. Gustav ;
Pfeufer, Arne ;
Sinner, Moritz F. ;
Lohman, Kurt ;
Ding, Jingzhong ;
Smith, Nicholas L. ;
Smith, Jonathan D. ;
Rienstra, Michiel ;
Rice, Kenneth M. ;
Van Wagoner, David R. ;
Magnani, Jared W. ;
Wakili, Reza ;
Clauss, Sebastian ;
Rotter, Jerome I. ;
Steinbeck, Gerhard ;
Launer, Lenore J. ;
Davies, Robert W. ;
Borkovich, Matthew ;
Harris, Tamara B. ;
Lin, Honghuang ;
Voelker, Uwe ;
Voelzke, Henry ;
Milan, David J. ;
Hofman, Albert ;
Boerwinkle, Eric ;
Chen, Lin Y. ;
Soliman, Elsayed Z. ;
Voight, Benjamin F. ;
Li, Guo ;
Chakravarti, Aravinda ;
Kubo, Michiaki ;
Tedrow, Usha B. ;
Rose, Lynda M. ;
Ridker, Paul M. ;
Conen, David .
NATURE GENETICS, 2012, 44 (06) :670-U88
[8]   EVIDENCE AGAINST A MYOCARDIAL FACTOR AS THE CAUSE OF LEFT-VENTRICULAR DILATION IN ACTIVE RHEUMATIC CARDITIS [J].
ESSOP, MR ;
WISENBAUGH, T ;
SARELI, P .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1993, 22 (03) :826-829
[9]  
Fever WSGoR, 2004, RHEUM FEV RHEUM HEAR
[10]   Left ventricular mechanics during and after acute rheumatic fever: Contractile dysfunction is closely related to valve regurgitation [J].
Gentles, TL ;
Colan, SD ;
Wilson, NJ ;
Biosa, R ;
Neutze, JM .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2001, 37 (01) :201-207