Chagasic antibodies induce cardiac COX-2/iNOS mRNA expression with PGE2/NO production

被引:10
作者
Ganzinelli, Sabrina
Borda, Enri
Joensen, Lilian
Sterin-Borda, Leonor [1 ]
机构
[1] Univ Buenos Aires, Pharmacol Unit, Sch Dent, Buenos Aires, DF, Argentina
关键词
Chagas' disease; Myocardial function; Autoantibodies; iNOS/COX-2; mRNA; Parasympathetic dysautonomia; PGE(2); MUSCARINIC ACETYLCHOLINE-RECEPTORS; OXIDE SIGNALING SYSTEM; TRYPANOSOMA-CRUZI; NITRIC-OXIDE; INTERLEUKIN-1-BETA REGULATION; AUTOANTIBODIES; PARTICIPATION; INFECTION; CYCLOOXYGENASE-2; INVOLVEMENT;
D O I
10.1016/j.ijcard.2008.02.008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We demonstrate that serum IgG in chagasic patients interacting with the second extracellular loop of human cardiac M-2 muscarinic acetylcholine receptors (M-2 mAChR) trigger the production of PGE(2) and NO, that in turn induces COX-2/iNOS mRNA expression. An association between serum anti-M-2 peptide IgG, anti-cardiac membrane IgG and PGE(2) levels (p < 0.05) in chagasic dysautonomic patients was observed. Thus, we establish that serum anti-mAChR autoantibodies and PGE(2) might be considered as early markers of Chagas' associated dysautonomia. Affinity purified anti-M-2 peptide IgG from chagasic sera, while stimulating myocardial M-2 mAChR, it exerts an increase on PGE(2) generation and NOS activity, as well as COX-2/iNOS isoforms mRNA expression. The expression of these genes is related with phosphoinositides (PIs), cGMP accumulation and PKC activity. Inhibition of these enzymes shows that chagasic autoantibodies up-regulation of COX-2/iNOS mRNA level is under the control of endogenous iNO/cGMP signaling system. These results provide a novel insight into the role that cholinoceptor antibodies play in the development of myocardial inflammation. To our knowledge, there has been no previous report showing that an antibody interacting with heart mAChR can act as expression inducer of proinflammatory mediators. (c) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:212 / 223
页数:12
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