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Erschienen in: Inflammation 3/2019

21.11.2018 | ORIGINAL ARTICLE

Neutrophil Cytosolic Factor 1 Contributes to the Development of Sepsis

verfasst von: Dei-fang Chen, Xiu-zhen Cui, Wen-ming Cao, Wen Meng

Erschienen in: Inflammation | Ausgabe 3/2019

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Abstract

To identify differentially expressed genes in sepsis and potential key role of reactive oxygen species (ROS) genes associated with sepsis. Gene expression dataset was available from GSE46599. Firstly, we screened the differentially expressed genes between sepsis and healthy samples. Then, the Database for Annotation, Visualization and Integrated Discovery (DAVID) online tools were utilized to perform gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analyses at the functional level. Differentially expressed genes mediating ROS levels were validated in the next investigation and analysis. We identified 1094 genes expressed differentially between normal and sepsis samples, including 655 upregulated genes and 439 downregulated genes. At the functional level, GO and KEGG pathway enrichment analysis showed that those differentially expressed genes were majorly associated with the immune response and metabolic process in sepsis. Further analysis revealed that neutrophil cytosolic factor 1(NCF1), a critical gene in the ROS system, upregulated in THP-1 cell and monocytes under lipopolysaccharides stimulation. Moreover, we identified the upregulation of NCF1 in a sepsis model. We screened the differentially expressed genes from the global level and identified NCF1 might be a critical target gene in sepsis.
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Metadaten
Titel
Neutrophil Cytosolic Factor 1 Contributes to the Development of Sepsis
verfasst von
Dei-fang Chen
Xiu-zhen Cui
Wen-ming Cao
Wen Meng
Publikationsdatum
21.11.2018
Verlag
Springer US
Erschienen in
Inflammation / Ausgabe 3/2019
Print ISSN: 0360-3997
Elektronische ISSN: 1573-2576
DOI
https://doi.org/10.1007/s10753-018-0935-z

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