Schulze Wolfgang, Kunze Rudolf, Wallukat Gerd
Max Delbrück Centre for Molecular Medicine;
Exp Clin Cardiol. 2005 Fall;10(3):170-2.
After more than 15 years of intensive research in the field of functional autoantibodies (AAB) directed against G-protein-coupled receptors, there is growing evidence of a causal involvement of AAB in various cardiovascular diseases such as dilated cardiomyopathy, peripartum cardiomyopathy, malignant and essential hypertension, and preeclampsia. It has been indicated that AAB against beta-1 adrenergic receptor, alpha-1 adrenergic receptor, angiotensin-II receptor AT(1) and muscarinic M(2)-receptors undergo agonist-like actions on the corresponding receptor and induce a permanent stimulation of G-protein-coupled signal cascades, which may cause Ca(2+) overload and cardiomyocyte destruction.Furthermore, the present review describes how G-protein-coupled receptor AAB are able to activate transcription factor nuclear factor-kappa B, which may regulate the expression of genes involved in immune and inflammatory responses.
在针对G蛋白偶联受体的功能性自身抗体(AAB)领域进行了15年多的深入研究之后,越来越多的证据表明AAB在各种心血管疾病中存在因果关系,如扩张型心肌病、围产期心肌病、恶性和原发性高血压以及先兆子痫。已经表明,针对β-1肾上腺素能受体、α-1肾上腺素能受体、血管紧张素-II受体AT(1)和毒蕈碱M(2)受体的AAB对相应受体具有激动剂样作用,并诱导G蛋白偶联信号级联的持续刺激,这可能导致Ca(2+)过载和心肌细胞破坏。此外,本综述描述了G蛋白偶联受体AAB如何能够激活转录因子核因子-κB,其可能调节参与免疫和炎症反应的基因的表达。