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Immune-Related Gene Expression Profile in Laboratory Common Marmosets Assessed by an Accurate Quantitative Real-Time PCR Using Selected Reference Genes

机译:通过使用选定参考基因的精确定量实时PCR评估的实验室普通mos猴中的免疫相关基因表达谱

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摘要

The common marmoset (Callithrix jacchus) is considered a novel experimental animal model of non-human primates. However, due to antibody unavailability, immunological and pathological studies have not been adequately conducted in various disease models of common marmoset. Quantitative real-time PCR (qPCR) is a powerful tool to examine gene expression levels. Recent reports have shown that selection of internal reference housekeeping genes are required for accurate normalization of gene expression. To develop a reliable qPCR method in common marmoset, we used geNorm applets to evaluate the expression stability of eight candidate reference genes (GAPDH, ACTB, rRNA, B2M, UBC, HPRT, SDHA and TBP) in various tissues from laboratory common marmosets. geNorm analysis showed that GAPDH, ACTB, SDHA and TBP were generally ranked high in stability followed by UBC. In contrast, HPRT, rRNA and B2M exhibited lower expression stability than other genes in most tissues analyzed. Furthermore, by using the improved qPCR with selected reference genes, we analyzed the expression levels of CD antigens (CD3ε, CD4, CD8α and CD20) and cytokines (IL-1β, IL-2, IL-4, IL-5, IL-6, IL-10, IL-12β, IL-13, IFN-γ and TNF-α) in peripheral blood leukocytes and compared them between common marmosets and humans. The expression levels of CD4 and IL-4 were lower in common marmosets than in humans whereas those of IL-10, IL-12β and IFN-γ were higher in the common marmoset. The ratio of Th1-related gene expression level to that of Th2-related genes was inverted in common marmosets. We confirmed the inverted ratio of CD4 to CD8 in common marmosets by flow cytometric analysis. Therefore, the difference in Th1/Th2 balance between common marmosets and humans may affect host defense and/or disease susceptibility, which should be carefully considered when using common marmoset as an experimental model for biomedical research.
机译:普通mar猴(Callithrix jacchus)被认为是非人类灵长类动物的新型实验动物模型。然而,由于抗体的缺乏,尚未在普通mar猴的各种疾病模型中进行充分的免疫学和病理学研究。实时定量PCR(qPCR)是检查基因表达水平的强大工具。最近的报道表明,需要选择内部参考管家基因来使基因表达准确归一化。为了开发在普通mar猴中可靠的qPCR方法,我们使用geNorm applet评估了八个普通参猴在各种组织中的八个候选参考基因(GAPDH,ACTB,rRNA,B2M,UBC,HPRT,SDHA和TBP)的表达稳定性。 geNorm分析表明,GAPDH,ACTB,SDHA和TBP的稳定性一般排名较高,其次是UBC。相反,在大多数分析的组织中, HPRT rRNA B2M 的表达稳定性低于其他基因。此外,通过使用带有选定参考基因的改良qPCR,我们分析了CD抗原(CD3ε,CD4,CD8α和CD20)和细胞因子(IL-1β,IL-2,IL-4,IL-5,IL- 6,IL-10,IL-12β,IL-13,IFN-γ和TNF-α),并在普通mar猴和人类之间进行了比较。在普通mar猴中,CD4和IL-4的表达水平低于人,而在普通mar猴中,IL-10,IL-12β和IFN-γ的表达水平较高。在普通mar猴中,Th1相关基因的表达水平与Th2相关基因的表达水平之比是相反的。我们通过流式细胞仪分析证实了普通mar猴中CD4与CD8的倒置比率。因此,普通mar猴与人之间的Th1 / Th2平衡差异可能会影响宿主防御和/或疾病易感性,在将普通as猴作为生物医学研究实验模型时应仔细考虑。

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