Kasahara H, Itoh M, Sugiyama T, Kido N, Hayashi H, Saito H, Tsukita S, Kato N
First Department of Internal Medicine, Nagoya University School of Medicine, Japan.
J Clin Invest. 1994 Sep;94(3):1026-36. doi: 10.1172/JCI117416.
Autoimmune myocarditis is considered to play a major role in the pathogenesis of dilated cardiomyopathy. A new autoimmune myocarditis model was attained by repeated immunization using murine cardiac C-protein with the immunological adjuvant, Klebsiella pneumoniae O3 lipopolysaccharide. For further analysis of a pathological epitope, the cDNA encoding C-protein was isolated; a fusion protein encoded by part of this cDNA induced myocarditis in SMA mice as well as in three other strains: DBA/1J (H-2q), O20/A (H-2pz1), and SJL (H-2s). The nucleotide sequence and its deduced amino acid analysis revealed that this protein had immunoglobulin-like and fibronectin-like repeats. This study provides a new animal model of autoimmune myocarditis which may shed light on the pathogenesis of dilated cardiomyopathy.
自身免疫性心肌炎被认为在扩张型心肌病的发病机制中起主要作用。通过使用鼠心脏C蛋白与免疫佐剂肺炎克雷伯菌O3脂多糖进行反复免疫,获得了一种新的自身免疫性心肌炎模型。为了进一步分析病理表位,分离出编码C蛋白的cDNA;该cDNA部分编码的融合蛋白在SMA小鼠以及其他三个品系:DBA/1J(H-2q)、O20/A(H-2pz1)和SJL(H-2s)中诱发了心肌炎。核苷酸序列及其推导的氨基酸分析表明,该蛋白具有免疫球蛋白样和纤连蛋白样重复序列。本研究提供了一种新的自身免疫性心肌炎动物模型,可能有助于阐明扩张型心肌病的发病机制。