[p38 MAPK/cPLA2 pathway mediates interleukins release in inflammatory cell model]

Zhongguo Wei Zhong Bing Ji Jiu Yi Xue. 2007 Jan;19(1):31-5.
[Article in Chinese]

Abstract

Objective: To explore the underlying mechanism of lipopolysaccharide (LPS)-induced interleukin-1 beta (IL-1 beta) and IL-6 release via p38 mitogen-activated protein kinase (MAPK) pathway in HeLa cells for further identification of involved down-stream message factors.

Methods: HeLa cells were challenged with LPS to reproduce inflammatory cell model. The activity or expression of p38 MAPK, cytosolic phospholipase A(2) (cPLA(2)) and COX-2, was inhibited with pretreatment of inflammatory HeLa cells with the inhibitors (SB203580, AACOCF(3), NS-398) or transfected with the cPLA(2) antisense oligonucleotide (SK7111), then the activities and/or expression of p38 MAPK, cPLA(2), COX-2, and relationship with levels of IL-1 beta and IL-6 supernatants were determined in each group.

Results: SB203580 obviously down-regulated the activities of p38 and cPLA(2), as well as the release of IL-1 beta and IL-6. AACOCF(3) and SK7111 blocked dose-dependently the activity or expression of cPLA(2), IL-1 beta and IL-6 production. However, the expression of COX-2 could hardly be detected in HeLa cells, even after LPS treatment. At the same time, pre-treatment with NS-398 had no effect on IL-1 beta, IL-6 production.

Conclusion: p38 MAPK/cPLA(2) pathway mediates the expression of IL-1 beta and IL-6 resulting from LPS treatment of HeLa cells, while COX-2, as a down-stream enzyme of cPLA(2) has no effect in this process.

Publication types

  • English Abstract
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cyclooxygenase 2 / metabolism*
  • HeLa Cells
  • Humans
  • Interleukin-1beta / metabolism*
  • Interleukin-6 / metabolism*
  • Lipopolysaccharides / pharmacology
  • Phospholipases A2, Cytosolic / metabolism*
  • p38 Mitogen-Activated Protein Kinases / metabolism*

Substances

  • Interleukin-1beta
  • Interleukin-6
  • Lipopolysaccharides
  • Cyclooxygenase 2
  • PTGS2 protein, human
  • p38 Mitogen-Activated Protein Kinases
  • Phospholipases A2, Cytosolic