Xu Hong-Fei, Meng Lin, Yao Jian, Gu Zhen-Yong, Liu Guo-Qing, Shen Yi-Wen, Zhao Zi-Qin
Department of Forensic Medicine, School of Biology and Basic Medical Sciences, Medical College of Soochow University, Suzhou 215123, China.
Fa Yi Xue Za Zhi. 2013 Jun;29(3):164-7.
To discuss the myocardial expression of Spry1 and MAPK proteins of viral myocarditis (VMC), to reveal its mechanism of sudden death, and to provide guides for forensic identification of sudden cardiac death.
Thirty Balb/c male mice were randomly divided into VMC group and control group, inoculated intraperitoneally with Coxsackievirus B3 and Eagel's solution, respectively. After the mice were sacrificed, the cardiac tissues of the mice were taken to proceed regular pathological examination. The changes of Spry1 protein, Spry1 mRNA and MAPK protein were detected by immunohistochemistry, Western blotting and real-time PCR.
Under light microscope, the pathologic changes included myocardial interstitial edema, inflammatory cells infiltration, myocardial necrosis, and focal and patchy necrosis of myocardial fiber in VMC group. The expression of Spry1 protein in VMC group was lower than that in control group (P < 0.05). There was slightly decreased expression of Spry1 of the mRNA level in VMC group (P > 0.05). But the MAPK protein expression in VMC group was higher than that in control group (P < 0.05).
The pathway of MAPK/ERK involving Spry1 protein accelerates the expression of collagen, which may contribute to arrhythmia, heart failure and even sudden cardiac death.
探讨病毒性心肌炎(VMC)中Spry1和丝裂原活化蛋白激酶(MAPK)蛋白的心肌表达情况,揭示其猝死机制,为心脏性猝死的法医学鉴定提供指导。
将30只Balb/c雄性小鼠随机分为VMC组和对照组,分别腹腔注射柯萨奇病毒B3和伊格尔液。小鼠处死后,取其心脏组织进行常规病理检查。采用免疫组织化学、蛋白质印迹法和实时荧光定量PCR检测Spry1蛋白、Spry1 mRNA和MAPK蛋白的变化。
光镜下,VMC组病理改变包括心肌间质水肿、炎性细胞浸润、心肌坏死以及心肌纤维局灶性和片状坏死。VMC组Spry1蛋白表达低于对照组(P<0.05)。VMC组mRNA水平的Spry1表达略有下降(P>0.05)。但VMC组MAPK蛋白表达高于对照组(P<0.05)。
涉及Spry1蛋白的MAPK/ERK信号通路加速胶原蛋白的表达,这可能导致心律失常、心力衰竭甚至心脏性猝死。