In:
Clinical and Experimental Immunology, Oxford University Press (OUP), Vol. 125, No. 1 ( 2001-12-20), p. 56-63
Abstract:
Interleukin (IL)-17 is a newly identified T cell-derived cytokine that can regulate the functions of a variety of cell types. In this study, we investigated the effects of IL-17 and interferon (IFN)-γ on chemokine secretion in human fetal intestinal epithelial cells. IL-8 and monocyte chemoattractant protein (MCP)-1 secretion by the human fetal intestinal epithelial cell line, intestine-407, was evaluated by ELISA and Northern blot. The expression of IL-17 receptor (R) was analysed by a binding assay using [125I]-labelled IL-17. The activation of nuclear factor-κB (NF-κB), NF-IL6 and AP-1 was assessed by an electrophoretic gel mobility shift assay (EMSA). IL-17 induced a dose-dependent increase in IL-8 and MCP-1 secretion. The inducing effects of IL-17 on IL-8 and MCP-1 mRNA abundance reached a maximum as early as 3 h, and then gradually decreased. IL-17 and IFN-γ synergistically increased IL-8 and MCP-1 secretion and mRNA abundance. IFN-γ induced a weak increase in IL-17 R mRNA abundance, and incubation with IFN-γ for 24 h enhanced [125I] -labelled IL-17-binding by 2·4-fold. IL-17 rapidly induced the phosphorylation and degradation of IκBα molecules, and the combination of IL-17 and IFN-γ induced a marked increase in NF-κB DNA-binding activity as early as 1·5 h after the stimulation. Furthermore, this combination induced an increase in NF-IL-6 and AP-1 DNA-binding activity. In conclusion, it becomes clear that IL-17 is an inducer of IL-8 and MCP-1 secretion by human fetal intestinal epithelial cells. The combination of IL-17 with IFN-γ synergistically enhanced chemokine secretion. These effects of IL-17 and IFN-γ might play an important role in the inflammatory responses in the intestinal mucosa.
Type of Medium:
Online Resource
ISSN:
1365-2249
,
0009-9104
DOI:
10.1046/j.1365-2249.2001.01588.x
Language:
English
Publisher:
Oxford University Press (OUP)
Publication Date:
2001
detail.hit.zdb_id:
2020024-9
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