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Expression of protease-activated receptor 2 in ulcerative colitis.

  • Jin A. Kim*
  • , Suck Chei Choi
  • , Ki Jung Yun
  • , Dae Ki Kim
  • , Myung Kwan Han
  • , Geom Seog Seo
  • , Ju Jin Yeom
  • , Tae Hyun Kim
  • , Yong Ho Nah
  • , Young Mi Lee
  • *Corresponding author for this work
  • Wonkwang University

Research output: Contribution to journalJournal articlepeer-review

Abstract

Although tryptase released from mast cells might play a key role in the pathogenesis of ulcerative colitis (UC), the role of protease-activated receptor 2 (PAR2), tryptase receptor, remains unclear in the pathogenesis of this disease. The expressions of PAR2 and tumor necrosis factor (TNF) alpha in nine UC tissues and nine normal tissues were examined by immunohistochemistry. TNF-alpha levels secreted from human leukemic mast cell line (HMC-1) after the treatment of PAR2 agonists were also measured by enzyme-linked immunosorbent assay. The PAR2 and TNF-alpha proteins were more significantly detectable in UC tissues than in normal tissues. Furthermore, 65.2% of PAR2+ cells and 66.4% of TNF-alpha+ cells in UC tissues were tryptase-positive cells. In other words, 60.6% and 46.3% of tryptase-positive cells in UC tissues were PAR2+ cells and TNF-alpha+ cells, respectively. A chi2 analysis showed correlation (p < 0.007) between PAR2 and TNF-alpha in tryptase-positive mast cells. Moreover, PAR2 agonists significantly induced the TNF-alpha secretion from HMC-1. These results indicate that the activation of the mast cells through PAR2 may be involved in the pathogenesis of UC.

Original languageEnglish
Pages (from-to)224-229
Number of pages6
JournalInflammatory bowel diseases
Volume9
Issue number4
DOIs
StatePublished - 2003.07

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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