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Gene expression profiles of adult peripheral and cord blood mononuclear cells altered by lipopolysaccharide

机译:脂多糖改变成年外周血和脐血单个核细胞的基因表达谱

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Background: Neonatal Gram-negative sepsis is often characterized by a fulminant clinical course, compared to adults, resulting in higher morbidity and mortality. Genome-wide gene expression analysis can provide insights into the molecular alterations in sepsis. Objectives: To evaluate in vitro activation of the neonatal and adult immune system, gene expression patterns were compared in mononuclear cells from cord (CBMNC) and adult peripheral blood (APBMNC). Methods: To better understand the influence of early molecular signals on the effects of sepsis, Affymetrix gene profiling (8,475 genes) was done on RNA isolated from CBMNC and APBMNC without and after incubation with 100 ng/ml lipopolysaccharide (LPS). Results: We demonstrated significant alterations in the expression of 108 CBMNC and APBMNC genes compared with basal levels, 188 significant changes in CBMNC and 97 in APBMNC, including cytokines, chemokines and immunoregulatory genes. Furthermore, we found 5 genes showing a significant interaction effect between cell type and LPS stimulation, including tumor necrosis factor receptor superfamily, member 6 (FAS), absent in melanoma 2, malic enzyme 1, hemoglobin ε 1, and trans-prenyltransferase. Conclusions: These results provide further support for a marked difference in the pathogenesis of neonatal and adult sepsis and may stimulate additional studies to investigate some of the altered genes as potential new targets for diagnostic tools and therapeutic strategies.
机译:背景:与成人相比,新生儿革兰氏阴性脓毒症的特点是临床病程繁重,从而导致更高的发病率和死亡率。全基因组基因表达分析可以为脓毒症的分子改变提供洞察力。目的:为了评估新生儿和成人免疫系统的体外激活,比较了脐带(CBMNC)和成人外周血(APBMNC)单核细胞中的基因表达模式。方法:为了更好地了解早期分子信号对败血症影响的影响,对未与100 ng / ml脂多糖(LPS)孵育和孵育后从CBMNC和APBMNC分离的RNA进行了Affymetrix基因谱分析(8,475个基因)。结果:与基础水平相比,我们证明了108个CBMNC和APBMNC基因表达的显着改变,包括细胞因子,趋化因子和免疫调节基因的CBMNC有188个显着变化,APBMNC有97个显着变化。此外,我们发现5个基因在细胞类型和LPS刺激之间显示出显着的相互作用,包括肿瘤坏死因子受体超家族,成员6(FAS),黑色素瘤2,苹果酸酶1,血红蛋白ε1和反异戊烯基转移酶中不存在。结论:这些结果为新生儿和成人败血症的发病机理上的显着差异提供了进一步的支持,并可能激发更多的研究来研究一些改变的基因,将其作为诊断工具和治疗策略的潜在新靶标。

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