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利用微阵列技术对急性排斥移植肾进行基因表达谱分析。

Gene expression profiling on acute rejected transplant kidneys with microarray.

作者信息

Li Deping, Wang Kang, Dai Yong, Lv Tianyu

机构信息

Hemopurification Department, Shenzhen People's Hospital, Shenzhen 518020, China.

出版信息

J Huazhong Univ Sci Technolog Med Sci. 2008 Apr;28(2):136-9. doi: 10.1007/s11596-008-0205-7. Epub 2008 May 15.

Abstract

To investigate the gene expression profiles in acute allograft rejection of renal transplantation, and identify the markers for the early diagnosis of acute rejection, heterotopic kidney transplantation was performed by using F344 or Lewis donors and Lewis recipients. No immunosuppressant was used. Renal grafts were harvested on days 3, 7, and 14. A commercial microarray was used to measure gene expression levels in day-7 grafts. The expression levels of 48 genes were up-regulated in the allograft in comparison with the isograft control, and interferon-gamma-induced GTPase gene was most significantly up-regulated in allografts. It is concluded that a variety of pathways are involved in organ transplant rejection which is dynamic and non-balanced. IFN-inducible genes, such as IGTP, may play an important role in the rejection. A lot of important factors involved in acute rejection are unnecessary but sufficient conditions for the rejection. We are led to conclude that it is virtually impossible to make an early diagnosis based on a single gene marker, but it could be achieved on the basis of a set of markers.

摘要

为研究肾移植急性同种异体排斥反应中的基因表达谱,并确定急性排斥反应早期诊断的标志物,采用F344或Lewis供体及Lewis受体进行异位肾移植。未使用免疫抑制剂。在第3、7和14天采集肾移植物。使用商业微阵列检测第7天移植物中的基因表达水平。与同基因移植对照相比,同种异体移植中48个基因的表达水平上调,其中干扰素-γ诱导的GTP酶基因在同种异体移植中上调最为显著。结论是,多种途径参与了器官移植排斥反应,这种反应是动态且不均衡的。IFN诱导基因,如IGTP,可能在排斥反应中起重要作用。许多参与急性排斥反应的重要因素是排斥反应的非必要但充分条件。我们由此得出结论,基于单一基因标志物几乎不可能进行早期诊断,但基于一组标志物则有可能实现。

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