Up-regulation of intestinal epithelial cell derived IL-7 expression by keratinocyte growth factor through STAT1/IRF-1, IRF-2 pathway

PLoS One. 2013;8(3):e58647. doi: 10.1371/journal.pone.0058647. Epub 2013 Mar 12.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't
  • Retracted Publication

MeSH terms

  • Animals
  • Cell Line
  • Cell Proliferation / drug effects
  • Epithelial Cells / cytology
  • Epithelial Cells / metabolism*
  • Fibroblast Growth Factor 7 / immunology
  • Fibroblast Growth Factor 7 / metabolism*
  • Fibroblast Growth Factor 7 / pharmacology
  • Humans
  • Immunity, Mucosal / drug effects
  • Immunity, Mucosal / physiology
  • Interferon Regulatory Factor-1 / immunology
  • Interferon Regulatory Factor-1 / metabolism*
  • Interleukin-7 / biosynthesis*
  • Interleukin-7 / immunology
  • Intestinal Mucosa / cytology
  • Intestinal Mucosa / immunology
  • Intestinal Mucosa / metabolism*
  • Mice
  • STAT1 Transcription Factor / immunology
  • STAT1 Transcription Factor / metabolism*
  • Signal Transduction*
  • Up-Regulation*

Substances

  • FGF7 protein, human
  • Fgf7 protein, mouse
  • IL7 protein, human
  • IRF1 protein, human
  • Interferon Regulatory Factor-1
  • Interleukin-7
  • Irf1 protein, mouse
  • STAT1 Transcription Factor
  • STAT1 protein, human
  • Stat1 protein, mouse
  • Fibroblast Growth Factor 7

Grants and funding

This study was supported by the National Natural Science Foundation of China (No. 30973113 to H.Y.; No. 81020108023 to H.Y.; No. 81000830 to Y.J.C.), and the Chongqing Science and Technology Commission International Key Collaboration Project (CSTC 201110008 to H.Y.). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.