Tominaga M, Matsumori A, Horie M, Yoshida H, Okada Y
Third Department of Internal Medicine, Faculty of Medicine, Kyoto University, Japan.
J Clin Invest. 1993 Mar;91(3):1231-4. doi: 10.1172/JCI116285.
The pathogenesis of myocarditis and dilated cardiomyopathy is though to involve autoimmunological processes and myocardial calcium overload. Serum containing antiheart antibodies associated with a murine model of myocarditis increased [Ca2+]i in guinea pig ventricular myocytes only in the presence of extracellular Ca2+. The antiheart antibody-positive serum activated Ca(2+)-permeable cation channels that were insensitive to dihydropyridines and membrane stretch. The permeability sequence was Ba2+ > Ca2+ > Na+ approximately K+, and the single-channel conductance to Ba2+ was 12 pS. The channel was activated by extracellular application of the serum during on-cell recording, which suggests that a soluble intracellular messenger may be involved. The antibody-positive serum did not alter voltage-gated Ca2+ currents. We propose that excess Ca entry in myocarditis and dilated cardiomyopathy results from activation of a Ca(2+)-permeable cationic channel by the autoantibodies.
心肌炎和扩张型心肌病的发病机制被认为涉及自身免疫过程和心肌钙超载。仅在细胞外钙存在的情况下,与心肌炎小鼠模型相关的含抗心脏抗体的血清才会增加豚鼠心室肌细胞中的[Ca2+]i。抗心脏抗体阳性血清激活了对二氢吡啶和膜拉伸不敏感的Ca(2+)通透阳离子通道。通透顺序为Ba2+ > Ca2+ > Na+ ≈ K+,且对Ba2+的单通道电导为12 pS。在细胞膜片钳记录过程中,通过在细胞外施加血清可激活该通道,这表明可能涉及一种可溶性细胞内信使。抗体阳性血清并未改变电压门控性Ca2+电流。我们提出,在心肌炎和扩张型心肌病中,过量的钙内流是由自身抗体激活Ca(2+)通透阳离子通道所致。