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http://purl.uniprot.org/citations/23554911http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/23554911http://www.w3.org/2000/01/rdf-schema#comment"

Background

Epithelial cells(EC)-derived interleukin-7 (IL-7) plays a crucial role in control of development and homeostasis of neighboring intraepithelial lymphocytes (IEL), and keratinocyte growth factor (KGF) exerts protective effects on intestinal epithelial cells and up-regulates EC-derived IL-7 expression through KGFR pathway. This study was to further investigate the molecular mechanism involved in the regulation of IL-7 expression by KGF in the intestine.

Methods

Intestinal epithelial cells (LoVo cells) and adult C57BL/6J mice were treated with KGF. Epithelial cell proliferation was studied by flow cytometry for BrdU-incorporation and by immunohistochemistry for PCNA staining. Western blot was used to detect the changes of expression of P-Tyr-STAT1, STAT1, and IL-7 by inhibiting STAT1. Alterations of nuclear extracts and total proteins of IRF-1, IRF-2 and IL-7 following IRF-1 and IRF-2 RNA interference with KGF treatment were also measured with western blot. Moreover, IL-7 mRNA expressions were also detected by Real-time PCR and IL-7 protein level in culture supernatants was measured by enzyme linked immunosorbent assay(ELISA).

Results

KGF administration significantly increased LoVo cell proliferation and also increased intestinal wet weight, villus height, crypt depth and crypt cell proliferation in mice. KGF treatment led to increased levels of P-Tyr-STAT1, RAPA and AG490 both blocked P-Tyr-STAT1 and IL-7 expression in LoVo cells. IRF-1 and IRF-2 expression in vivo and in vitro were also up-regulated by KGF, and IL-7 expression was decreased after IRF-1 and IRF-2 expression was silenced by interfering RNA, respectively.

Conclusion

KGF could up-regulate IL-7 expression through the STAT1/IRF-1, IRF-2 signaling pathway, which is a new insight in potential effects of KGF on the intestinal mucosal immune system."xsd:string
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http://purl.uniprot.org/citations/23554911http://purl.uniprot.org/core/author"Yang H."xsd:string
http://purl.uniprot.org/citations/23554911http://purl.uniprot.org/core/author"Yang Y."xsd:string
http://purl.uniprot.org/citations/23554911http://purl.uniprot.org/core/author"Sun L.H."xsd:string
http://purl.uniprot.org/citations/23554911http://purl.uniprot.org/core/author"Wang W.S."xsd:string
http://purl.uniprot.org/citations/23554911http://purl.uniprot.org/core/author"Cai Y.J."xsd:string
http://purl.uniprot.org/citations/23554911http://purl.uniprot.org/core/author"Teitelbaum D.H."xsd:string
http://purl.uniprot.org/citations/23554911http://purl.uniprot.org/core/date"2013"xsd:gYear
http://purl.uniprot.org/citations/23554911http://purl.uniprot.org/core/name"PLoS One"xsd:string
http://purl.uniprot.org/citations/23554911http://purl.uniprot.org/core/pages"e58647"xsd:string
http://purl.uniprot.org/citations/23554911http://purl.uniprot.org/core/title"Up-regulation of intestinal epithelial cell derived IL-7 expression by keratinocyte growth factor through STAT1/IRF-1, IRF-2 pathway."xsd:string
http://purl.uniprot.org/citations/23554911http://purl.uniprot.org/core/volume"8"xsd:string
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