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Neutrophil-derived IL-1? is sufficient for abscess formation in immunity against Staphylococcus aureus in mice.


ABSTRACT: Neutrophil abscess formation is critical in innate immunity against many pathogens. Here, the mechanism of neutrophil abscess formation was investigated using a mouse model of Staphylococcus aureus cutaneous infection. Gene expression analysis and in vivo multispectral noninvasive imaging during the S. aureus infection revealed a strong functional and temporal association between neutrophil recruitment and IL-1?/IL-1R activation. Unexpectedly, neutrophils but not monocytes/macrophages or other MHCII-expressing antigen presenting cells were the predominant source of IL-1? at the site of infection. Furthermore, neutrophil-derived IL-1? was essential for host defense since adoptive transfer of IL-1?-expressing neutrophils was sufficient to restore the impaired neutrophil abscess formation in S. aureus-infected IL-1?-deficient mice. S. aureus-induced IL-1? production by neutrophils required TLR2, NOD2, FPR1 and the ASC/NLRP3 inflammasome in an ?-toxin-dependent mechanism. Taken together, IL-1? and neutrophil abscess formation during an infection are functionally, temporally and spatially linked as a consequence of direct IL-1? production by neutrophils.

SUBMITTER: Cho JS 

PROVIDER: S-EPMC3510260 | biostudies-literature | 2012

REPOSITORIES: biostudies-literature

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Neutrophil abscess formation is critical in innate immunity against many pathogens. Here, the mechanism of neutrophil abscess formation was investigated using a mouse model of Staphylococcus aureus cutaneous infection. Gene expression analysis and in vivo multispectral noninvasive imaging during the S. aureus infection revealed a strong functional and temporal association between neutrophil recruitment and IL-1β/IL-1R activation. Unexpectedly, neutrophils but not monocytes/macrophages or other M  ...[more]

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