首页> 外文期刊>Journal of Medical Colleges of PLA >TaqMan real-time fluorescent quantitative RT-PCR in detection of macrophage inflammatory protein-2γ mRNA in myocarditis murine
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TaqMan real-time fluorescent quantitative RT-PCR in detection of macrophage inflammatory protein-2γ mRNA in myocarditis murine

机译:TaqMan实时荧光定量RT-PCR检测心肌炎小鼠巨噬细胞炎症蛋白2γmRNA

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Objective: To study the role of macrophage inflammatory protein ( MIP)-2γ in myocarditis pathogenesis in BALB/c mice. Methods: The relationship, between the progression of Coxsarckie virus B_3 (CVB_3) viral myocarditis and experimental autoimmune myocarditis and MIP-2γ mRNA expression in mouse was studied by TaqMan real-time fluorescent quantitative RT-PCR. Results: MIP-2γ mRNA expression rose on 3 to 5 d after CVB_3 infection, reached peak on 7 d, and returned to normal level until 14 d, which corresponded well with the disease course. The MIP-2γ mRNA expression level rose significantly on the day 18 d after immunization with porcine cardiac myosin which was consistent with pathological examination. Conclusion: MIP-2γ may be involved in the pathogenesis of myocarditis.
机译:目的:研究巨噬细胞炎症蛋白(MIP)-2γ在BALB / c小鼠心肌炎发病中的作用。方法:采用TaqMan实时荧光定量RT-PCR技术研究Coxsarckie病毒B_3(CVB_3)病毒性心肌炎的进展与小鼠自身免疫性心肌炎及MIP-2γmRNA表达之间的关系。结果:CVB_3感染后3〜5 d,MIP-2γmRNA表达上升,至7 d达到高峰,直至14 d恢复正常,与病程相吻合。猪心肌肌球蛋白免疫后第18天,MIP-2γmRNA表达水平明显升高,这与病理检查一致。结论:MIP-2γ可能参与了心肌炎的发病机制。

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