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Th1相关细胞因子在缺血再灌注诱导的肾损伤中起关键作用。

Critical involvement of Th1-related cytokines in renal injuries induced by ischemia and reperfusion.

作者信息

de Paiva Vanessa Nunes, Monteiro Rebecca M M, Marques Vilmar de Paiva, Cenedeze Marcos Antonio, Teixeira Vicente de P A, dos Reis Marlene A, Pacheco-Silva Alvaro, Câmara Niels O S

机构信息

Laboratory of Clinical and Experimental Immunology. Nephrology Division, Department of Medicine, Universidade Federal de São Paulo UNIFESP-EPM, São Paulo, Brazil.

出版信息

Int Immunopharmacol. 2009 Jun;9(6):668-72. doi: 10.1016/j.intimp.2008.11.012. Epub 2008 Dec 16.

Abstract

Renal ischemia and reperfusion injury (IRI) is considered an inflammatory syndrome. To move forward in its pathogenesis, we exploited the role of several cytokines on renal damages triggered by IRI. Specifically to evaluate the role of Th1 immune profile in this system, IL-12, IFN-gamma, and IFN-gamma/IL-12 deficient (KO) mice on C57BL/6 background and their controls were subjected to IRI. In each group, blood and kidney samples were harvested. Renal function was evaluated by serum creatinine and renal morphometric analyses. Gene expression of IL-6 and HO-1 were also investigated by Q-PCR. IFN-gamma KO animals presented the highest impairment in renal function compared to controls. Conversely, IL-12 KO animals were absolutely protected and, in a lesser extent, IFN-gamma/IL-12 KO double knockout was also protected from IRI. Gene expression analyses showed higher expression of HO-1, a cytoprotective gene, and IL-6, a pro-inflammatory cytokine, in IFN-gamma deficient animals subjected to IRI. Our results confirm that Th1 related cytokines such as IL-12 and IFN-gamma are critically involved in renal ischemia and reperfusion injury.

摘要

肾缺血再灌注损伤(IRI)被认为是一种炎症综合征。为了深入了解其发病机制,我们探讨了几种细胞因子在IRI引发的肾损伤中的作用。具体而言,为了评估Th1免疫谱在该系统中的作用,我们将C57BL/6背景的IL-12、IFN-γ和IFN-γ/IL-12基因缺陷(KO)小鼠及其对照进行IRI处理。每组均采集血液和肾脏样本。通过血清肌酐和肾脏形态计量分析评估肾功能。还通过定量聚合酶链反应(Q-PCR)研究IL-6和血红素加氧酶-1(HO-1)的基因表达。与对照组相比,IFN-γ基因敲除动物的肾功能损害最为严重。相反,IL-12基因敲除动物完全受到保护,并且在较小程度上,IFN-γ/IL-12基因双敲除动物也免受IRI损伤。基因表达分析显示,在遭受IRI的IFN-γ缺陷动物中,细胞保护基因HO-1和促炎细胞因子IL-6的表达较高。我们的结果证实,IL-12和IFN-γ等与Th1相关的细胞因子在肾缺血再灌注损伤中起关键作用。

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