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Identification of a novel diagnostic marker for viral myocarditis using cDNA microarrays.

机译:使用cDNA芯片鉴定病毒性心肌炎的新型诊断标记。

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摘要

The Coxsackievirus B3 (CVB3) serotype is the leading cause of viral myocarditis. Presently, the Dallas Criteria is the gold standard for diagnosis. In the present study, we utilized microarrays to search for differentially expressed genes between CVB3-infected mice and control mice in order to identify novel diagnostic targets. A/J mice were infected with 10pfu of CVB3. Total RNA was extracted from heart tissue and analyzed by cDNA microarray. The Aldo-Keto Reductase AKR1C13 gene was found to have the greatest degree of upregulation following reverse labeling (Floor Flip) and was independently confirmed using real time RT-PCR. Microarray conducted on blood samples also showed AKR1C13 to be upregulated. Microarrays conducted on AB and MI mice showed no change in the expression of AKR1C13. AKR1C4 occupies the syntenic region of AKR1C13 in the human genome and was shown to be upregulated in human biopsy samples of myocarditis when examined by RT-PCR. We have identified the Aldo-Keto Reductase AYR1C4 gene as a possible candidate for use as a diagnostic tool in human myocarditis.
机译:柯萨奇病毒B3(CVB3)血清型是病毒性心肌炎的主要原因。当前,达拉斯标准是诊断的金标准。在本研究中,我们利用微阵列搜索CVB3感染小鼠和对照小鼠之间差异表达的基因,以鉴定新的诊断靶标。用10pfu的CVB3感染A / J小鼠。从心脏组织中提取总RNA,并通过cDNA微阵列分析。发现Aldo-Keto还原酶AKR1C13基因在反向标记(Floor Flip)后具有最大的上调程度,并使用实时RT-PCR进行了独立确认。在血液样本上进行的微阵列分析也表明AKR1C13被上调。在AB和MI小鼠上进行的微阵列显示AKR1C13的表达没有变化。 AKR1C4在人类基因组中占据AKR1C13的同位区域,并通过RT-PCR检测显示在人类活检心肌炎样本中AKR1C13被上调。我们已经确定了醛糖-酮还原酶AYR1C4基因可能用作人类心肌炎的诊断工具。

著录项

  • 作者

    Cerullo, Dante.;

  • 作者单位

    University of Toronto (Canada).;

  • 授予单位 University of Toronto (Canada).;
  • 学科 Health Sciences Pathology.; Biology Microbiology.
  • 学位 M.Sc.
  • 年度 2003
  • 页码 p.924
  • 总页数 162
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 病理学;
  • 关键词

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