Effects of IgM from rheumatic fever patients on intracellular calcium levels of neonatal rat cardiac myocytes

被引:2
作者
Bick, RJ
Poindexter, BJ
Tong, S
Kalis, NN
Van der Merwe, P
Gatchel, J
Young, DC
机构
[1] Univ Texas, Hlth Sci Ctr, Dept Pathol, Houston, TX 77030 USA
[2] Univ Stellenbosch, Dept Pediat & Child Hlth, ZA-7505 Tygerberg, South Africa
关键词
rheumatic heart disease; antibodies; calcium channels;
D O I
10.1016/S0024-3205(03)00560-5
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 [基础医学];
摘要
Rheumatic fever (RF), a potential sequela of Streptococcus pyogenes pharyngitis, sometimes results in myocarditis and heart failure. Antibodies have been implicated in the pathogenesis of RF and anti-cardiac myosin antibody levels are elevated in RF patients. Since myocarditis is associated with altered cardiomyocyte calcium transients it was of interest to determine the direct effects of RF patient antibodies on calcium transients in cultured myocytes. RF patient polyclonal IgM treatment caused increased calcium retention by neonatal rat heart cells in vitro as determined with isotopically labeled calcium. Therefore, to further characterize this finding, calcium transients were evaluated by real time fluorescence spectroscopy and deconvolution imaging. RF patient polyclonal IgM produced increased calcium retention during the relaxation stage of the contraction cycle leading to a slowing of contraction rate, disorganized calcium transients, and eventual tetany. In contrast, calcium transient studies of cardiomyocytes following treatment with monoclonal anti-myosin antibodies revealed declining intracellular calcium levels, accompanied by disorganized transients and tetany. Treatment with both antibodies led to myocyte dysfunction and these novel findings suggest a role for antibodies in the pathogenesis of the myocarditis associated with rheumatic carditis. (C) 2003 Elsevier Inc. All fights reserved.
引用
收藏
页码:2101 / 2111
页数:11
相关论文
共 25 条
[1]
Adderson EE, 1998, J IMMUNOL, V161, P2020
[2]
Antone SM, 1997, J IMMUNOL, V159, P5422
[3]
Mitochondrial participation in the intracellular Ca2+ network [J].
Babcock, DF ;
Herrington, J ;
Goodwin, PC ;
Park, YB ;
Hille, B .
JOURNAL OF CELL BIOLOGY, 1997, 136 (04) :833-844
[4]
Cytokines increase neonatal cardiac myocyte calcium concentrations: The involvement of nitric oxide and cyclic nucleotides [J].
Bick, RJ ;
Wood, DE ;
Poindexter, B ;
McMillin, JB ;
Karoly, A ;
Wang, DC ;
Bunting, R ;
McCann, T ;
Law, GJ ;
Buja, LM .
JOURNAL OF INTERFERON AND CYTOKINE RESEARCH, 1999, 19 (06) :645-653
[5]
BICK RJ, 1998, CARDIOVASC PATHOBIOL, V2, P159
[6]
STUDY OF HEART-REACTIVE ANTIBODY IN ANTISERA AND HYBRIDOMA CULTURE FLUIDS AGAINST GROUP-A STREPTOCOCCI [J].
CUNNINGHAM, MW ;
RUSSELL, SM .
INFECTION AND IMMUNITY, 1983, 42 (02) :531-538
[7]
EPITOPES OF STREPTOCOCCAL M-PROTEINS SHARED WITH CARDIAC MYOSIN [J].
DALE, JB ;
BEACHEY, EH .
JOURNAL OF EXPERIMENTAL MEDICINE, 1985, 162 (02) :583-591
[8]
AUTOIMMUNE DETERMINANTS OF RHEUMATIC CARDITIS - LOCALIZATION OF EPITOPES IN HUMAN CARDIAC MYOSIN [J].
DELL, A ;
ANTONE, SM ;
GAUNTT, CJ ;
CROSSLEY, CA ;
CLARK, WA ;
CUNNINGHAM, MW .
EUROPEAN HEART JOURNAL, 1991, 12 :158-162
[9]
Cytotoxic mAb from rheumatic carditis recognizes heart valves and laminin [J].
Galvin, JE ;
Hemric, ME ;
Ward, K ;
Cunningham, MW .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 106 (02) :217-224
[10]
Induction of myocarditis and valvulitis in Lewis rats by different epitopes of cardiac myosin and its implications in rheumatic carditis [J].
Galvin, JE ;
Hemric, ME ;
Kosanke, SD ;
Factor, SM ;
Quinn, A ;
Cunningham, MW .
AMERICAN JOURNAL OF PATHOLOGY, 2002, 160 (01) :297-306