Li Ya, Heuser Janet S, Cunningham Luke C, Kosanke Stanley D, Cunningham Madeleine W
Department of Microbiology and Immunology, University of Oklahoma Health Sciences Center, Biomedical Research Center, 975 NE 10th Street, Oklahoma City, OK 73104, USA.
J Immunol. 2006 Dec 1;177(11):8234-40. doi: 10.4049/jimmunol.177.11.8234.
The mechanisms by which autoantibodies against cardiac myosin (CM) may lead to heart dysfunction is unknown. We show that autoantibodies to CM in anti-CM sera and mAbs derived from experimental autoimmune myocarditis targeted the heart cell surface and induced Ab-mediated cAMP-dependent protein kinase A activity. Ab-mediated cell signaling of protein kinase A was blocked by CM, anti-IgG, or by specific inhibitors of the beta-adrenergic receptor (beta-AR) pathway. mAbs confirmed mimicry between CM and the beta-AR. Passive transfer of purified Ab (IgG) from CM-immunized rats resulted in IgG deposition and apoptosis in the heart, leading to a cardiomyopathic heart disease phenotype in recipients. Our novel findings link anti-CM Ab with the beta-AR and subsequent Ab-mediated cell signaling in the heart.
抗心肌肌凝蛋白(CM)自身抗体导致心脏功能障碍的机制尚不清楚。我们发现,抗CM血清中的抗CM自身抗体以及源自实验性自身免疫性心肌炎的单克隆抗体靶向心脏细胞表面,并诱导抗体介导的环磷酸腺苷(cAMP)依赖性蛋白激酶A活性。蛋白激酶A的抗体介导细胞信号传导被CM、抗IgG或β-肾上腺素能受体(β-AR)途径的特异性抑制剂阻断。单克隆抗体证实了CM与β-AR之间的模拟作用。将来自CM免疫大鼠的纯化抗体(IgG)被动转移导致心脏中IgG沉积和细胞凋亡,从而使受体出现心肌病心脏病表型。我们的新发现将抗CM抗体与β-AR以及随后心脏中的抗体介导细胞信号传导联系起来。