PMA-induced up-regulation of MMP-9 is regulated by a PKCalpha-NF-kappaB cascade in human lung epithelial cells

Exp Mol Med. 2007 Feb 28;39(1):97-105. doi: 10.1038/emm.2007.11.

Abstract

Expression of matrix metalloproteinase-9 (MMP-9) is associated with airway remodeling and tissue injury in asthma. However, little is known about how MMP-9 is up-regulated in airway epithelial cells. In this study, we show that phorbol myristate acetate (PMA) induces MMP-9 expression via a protein kinase Calpha (PKCalpha)-dependent signaling cascade in BEAS-2B human lung epithelial cells. Pretreatment with either GF109203X, a general PKC inhibitor, or Go6976, a PKCalpha/beta isozyme inhibitor, inhibited PMA-induced activation of the MMP-9 promoter, as did transient transfection with PKCalpha antisense oligonuclotides. PMA activated NF-kappaB by phosphorylating IkappaB in these cells and this was also inhibited by GF109203X and Go6976, suggesting that PKCa acts as an upstream regulator of NF-kappaB in PMA-induced MMP-9 induction. Our results indicate that a "PKCalpha-NF- kappaB"-dependent cascade is involved in the signaling leading to PMA-induced MMP-9 expression in the lung epithelium.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line
  • Epithelial Cells / drug effects
  • Epithelial Cells / metabolism
  • Humans
  • Lung / drug effects
  • Lung / metabolism*
  • Matrix Metalloproteinase 9 / metabolism*
  • NF-kappa B / metabolism*
  • Protein Kinase C-alpha / metabolism*
  • Tetradecanoylphorbol Acetate / pharmacology*
  • Up-Regulation / drug effects*

Substances

  • NF-kappa B
  • Protein Kinase C-alpha
  • Matrix Metalloproteinase 9
  • Tetradecanoylphorbol Acetate