Gene expression in human neutrophils during activation and priming by bacterial lipopolysaccharide
Department of Pediatrics
Medical Subject Headings
Cluster Analysis; Escherichia coli; Gene Expression; Gene Expression Profiling; Humans; Lipopolysaccharides; Multigene Family; Neutrophil Activation; Neutrophils; Oligonucleotide Array Sequence Analysis; RNA
Hematology | Oncology | Pediatrics
Circulating neutrophils play a key role both in the systemic inflammatory response and in complications of bacterial infection such as septic shock and septic multiple organ dysfunction syndrome. We have analyzed gene expression patterns in human neutrophils stimulated by E. coli lipopolysaccharide (LPS), with or without prior exposure to LPS, using differential display and oligonucleotide chip techniques. We identified 307 genes that were activated or repressed after treatment with LPS at 10 ng/ml and 385 genes after LPS at 100 ng/ml, compared with untreated neutrophils. The two sets included many transcription factors, cytokines, chemokines, interleukins, and surface antigens, as well as members of the toll-like receptor, Rel/NF-kappaB, and immune mediator gene families. Time course analysis showed that the early and late neutrophil responses to LPS share some common mechanisms, but many changes in gene expression are transient or late to develop. Neutrophils also showed a priming response to LPS, in which 97 genes significantly changed expression on re-exposure to lower dose LPS and were analyzed by unsupervised hierarchical clustering. These findings indicate that the neutrophil is a transcriptionally active cell responsive to environmental stimuli and capable of a complex series of both early and late changes in gene expression. Supplementary material for this article can be found on the Journal of Cellular Biochemistry website (http://jws-edci.interscience.wiley.com:8998/jpages/0730-2312/suppmat/89/v 89.page.html).
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Citation: J Cell Biochem. 2003 Jul 1;89(4):848-61. doi 10.1002/jcb.10526