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Data on changes of NF-κB gene expression in liver and lungs as a biomarker and hepatic injury in CLP-induced septic rats

机译:CLP诱导的脓毒症大鼠肝脏和肺中NF-κB基因表达变化作为生物标志物和肝损伤的数据

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Nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) is a ubiquitous transcription factor, which plays a key role in regulating immune response against infection. Increased and/or prolonged activation of NF-κB has been linked to cancer, inflammatory, autoimmune diseases and viral infection. The purpose of this set of data was to evaluate NF-κB gene expression in cecal ligation and puncture (CLP)- induced septic rats and associated hepatic cell changes. Here, we provide the information about the evaluation of NF-κB gene expression using Real-time PCR and histopathological data of liver-related to our study published in the Turkish Journal of Medical Sciences [1]. Also, the information of the primers and more details about gene expression evaluation by real-time PCR of the targeted gene is provided. The data present here introduced another biomarker in liver and lung of CLP- induced septic rats and also confirmed hepatic dysfunction based on the pathological data. The histopathologic assessment showed normal condition in control group, mild infiltration of neutrophils in the liver parenchyma and portal tracts in LAP group (laparotomy) but severe congestion, severe neutrophil infiltration in the liver parenchyma and portal tracts in the CLP group. The data from real-time PCR showed that NF-κB expression was significantly increased in the CLP group compared with the control and LAP group, so it can be a biomarker for (CLP)- induced sepsis. This set of data and our previous study underscored the powerful potential of using the real-time PCR method to determine the involvement of genes such as MPO, CD177, and NF-κB in infectious diseases like sepsis.
机译:激活的B细胞核因子κ轻链增强子(NF-κB)是一种普遍存在的转录因子,在调节针对感染的免疫反应中起关键作用。 NF-κB活化的增加和/或延长与癌症,炎性疾病,自身免疫性疾病和病毒感染有关。这组数据的目的是评估盲肠结扎和穿刺(CLP)诱导的败血症大鼠中NF-κB基因的表达以及相关的肝细胞变化。在这里,我们提供有关使用实时PCR评估NF-κB基因表达的信息以及与我们在《土耳其医学杂志》上发表的研究相关的肝脏组织病理学数据[1]。而且,提供了引物的信息以及有关通过靶基因的实时PCR进行基因表达评估的更多细节。此处提供的数据在CLP诱导的脓毒症大鼠的肝和肺中引入了另一种生物标志物,并根据病理数据证实了肝功能障碍。组织病理学评估显示,对照组正常,LAP组肝实质和门脉轻度中性粒细胞浸润(开腹术),而CLP组肝实质和门脉严重充血,中性粒细胞严重浸润。实时PCR的数据显示,与对照组和LAP组相比,CLP组的NF-κB表达显着增加,因此它可以作为(CLP)诱导的败血症的生物标志物。这组数据和我们先前的研究强调了使用实时PCR方法确定MPO,CD177和NF-κB等基因与败血症等传染病有关的强大潜力。

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