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Soluble ST2 protein inhibits LPS stimulation on monocyte-derived dendritic cells

ST2 protein is a soluble splicing variant of ST2L protein, which is the receptor for interleukin-33 (IL-33). Previously, we reported that soluble ST2 suppressed the signal transduction of lipopolysaccharide (LPS) and cytokine production in monocytic cells. To investigate whether or not this inhibito...

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Bibliographic Details
Published in:Cellular & molecular immunology 2012-09, Vol.9 (5), p.399-409
Main Authors: Nagata, Akihisa, Takezako, Naoki, Tamemoto, Hiroyuki, Ohto-Ozaki, Hiromi, Ohta, Satoshi, Tominaga, Shin-ichi, Yanagisawa, Ken
Format: Article
Language:English
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Summary:ST2 protein is a soluble splicing variant of ST2L protein, which is the receptor for interleukin-33 (IL-33). Previously, we reported that soluble ST2 suppressed the signal transduction of lipopolysaccharide (LPS) and cytokine production in monocytic cells. To investigate whether or not this inhibitory effect occurs in dendritic cells, which are the key players in innate and adaptive immunity, human monocyte-derived dendritic cells were pre-treated with soluble ST2 protein before LPS stimulation. Although soluble ST2 did not attenuate the LPS-induced maturation of dendritic cells, pre-treatment with soluble ST2 suppressed cytokine production and inhibited LPS signaling. Moreover, the proliferation of naive T cells was inhibited significantly by soluble ST2 pre-treatment. IL-33 had little effect on the cytokine production of immature monocyte-derived dendritic cells. Furthermore, soluble ST2 protein was internalized into dendritic cells, suggesting that soluble ST2 protein acts by a noncanonical mechanism other than the sequestration of IL-33.
ISSN:1672-7681
2042-0226
DOI:10.1038/cmi.2012.29