[Molecular mechanism of interleukin-13-induced mucus hypersecretion in rat airway]

Nan Fang Yi Ke Da Xue Xue Bao. 2011 Jan;31(1):73-6.
[Article in Chinese]

Abstract

Objective: To investigate the effect of interleukin-13 (IL-13) on mucus secretion in vivo and the possible mechanism.

Methods: The SD rats were randomly divided into control group, IL-13 group and IL-13 plus SP600125 group. The phosphorylation of extracellular signal-regulated kinase 1/2 (ERK1/2), c-Jun N-terminal kinase 1/2 (JNK1/2) and the level of MUC5AC in the lung tissues were examined using Western blotting. RT-PCR was performed to examine the mRNA level of STAT4 and STAT6, and electrophoretic mobility shift assays (EMSA) was used to detect the DNA-binding activities of Forkhead box a2 (FOXA2) and activator protein-1 (AP-1).

Results: IL-13 caused a significant increase in MUC5AC and p-JNK1/2 expression, but did not affect the phosphorylation of ERK1/2. The expression of MUC5AC was attenuated after treatment with SP600125. A significant increase in STAT6 was observed in IL-13 group compared with that in the control group, whereas the expression of STAT4 mRNA was not significantly affected. The DNA-binding activity of FOXA2 was down-regulated after IL-13 exposure, which did not affect the DNA-binding activity of AP-1.

Conclusion: IL-13 down-regulates mucus secretion via STAT6-FOXA2 pathway in vitro.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bronchi / metabolism*
  • Female
  • Hepatocyte Nuclear Factor 3-beta / genetics
  • Hepatocyte Nuclear Factor 3-beta / metabolism
  • Interleukin-13 / pharmacology*
  • Male
  • Mucin 5AC / metabolism
  • Mucus / metabolism*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Random Allocation
  • Rats
  • Rats, Sprague-Dawley
  • STAT6 Transcription Factor / genetics
  • STAT6 Transcription Factor / metabolism
  • Signal Transduction / drug effects

Substances

  • Foxa2 protein, rat
  • Interleukin-13
  • Muc5ac protein, rat
  • Mucin 5AC
  • RNA, Messenger
  • STAT6 Transcription Factor
  • Hepatocyte Nuclear Factor 3-beta