Kawamoto Osamu, Michiue Tomomi, Ishikawa Takaki, Maeda Hitoshi
Department of Legal Medicine, Osaka City University Medical, School, Osaka, Japan.
Department of Legal Medicine, Osaka City University Medical, School and Forensic Autopsy Section, Medico-legal Consultation and Postmortem Investigation Support Center (MLCPI-SC), Osaka, Japan.
Histol Histopathol. 2014 Jun;29(6):767-75. doi: 10.14670/HH-29.767. Epub 2013 Dec 24.
Immunohistochemistry of the terminal complement complex (C5b-9) and fibronectin (FN) is useful to detect myocardial ischemia preceding necrosis in the postmortem diagnosis of sudden cardiac death. The present immunohistochemical study examined connexin43 (Cx43) and zonula occludens-1 (ZO-1) as markers of early myocardial ischemia in addition to the above-mentioned markers, using forensic autopsy cases of acute deaths due to myocardial infarction (MI, n=15) and acute ischemic heart disease (AIHD) without apparent myocardial necrosis (n=8), compared with those of acute mechanical asphyxiation (As, n=24) and drowning (D, n=10) as controls. Immunopositivities of each marker in the myocardium were semi-quantitatively graded by scoring. ZO-1, C5b-9 and FN were detected in the myocardial cytoplasm, whereas Cx43 and non-phosphorylated (np) Cx43 showed varied localizations at the intercalated disc, in the cytoplasm and along the lateral cell border. ZO-1 and FN showed a tendency to be detected more intensely in MI and IHD than in As and D. C5b-9 showed specific staining at the site of ischemia in MI (n=10/15) and AIHD (n=6/8), while the distribution of npCx43 was different in most cases of MI (n=14/15) and AIHD (n=5/8), compared with As and D; npCx43 positivity score was higher in the cytoplasm than at the intercalated disc, indicating redistribution due to myocardial ischemia. Such findings were detected in a few cases of As (n=3/24). These findings suggest that the combination of npCx43 and C5b-9 immunohistochemistry is useful for detecting early lesions of myocardial ischemia in sudden cardiac death.
在心脏性猝死的尸检诊断中,终末补体复合物(C5b - 9)和纤连蛋白(FN)的免疫组织化学有助于检测坏死前的心肌缺血。本免疫组织化学研究,除上述标志物外,还检测了连接蛋白43(Cx43)和紧密连接蛋白1(ZO - 1)作为早期心肌缺血的标志物,使用心肌梗死(MI,n = 15)和无明显心肌坏死的急性缺血性心脏病(AIHD,n = 8)导致急性死亡的法医尸检病例,并与急性机械性窒息(As,n = 24)和溺水(D,n = 10)作为对照。通过评分对心肌中每种标志物的免疫阳性进行半定量分级。ZO - 1、C5b - 9和FN在心肌细胞质中被检测到,而Cx43和非磷酸化(np)Cx43在闰盘、细胞质和细胞侧边界处表现出不同的定位。ZO - 1和FN在MI和IHD中比在As和D中更倾向于被强烈检测到。C5b - 9在MI(n = 10/15)和AIHD(n = 6/8)的缺血部位显示特异性染色,而与As和D相比,npCx43的分布在大多数MI(n = 14/15)和AIHD(n = 5/8)病例中有所不同;npCx43阳性评分在细胞质中高于闰盘,表明由于心肌缺血导致重新分布。在少数As病例(n = 3/24)中也检测到了这些发现。这些发现表明,npCx43和C5b - 9免疫组织化学的联合应用有助于检测心脏性猝死中心肌缺血的早期病变。