Lipoxin A(4) inhibits transition of epithelial to mesenchymal cells in proximal tubules

Am J Nephrol. 2010;32(2):122-36. doi: 10.1159/000315121. Epub 2010 Jun 25.

Abstract

Background: Previous studies showed that connective tissue growth factor (CTGF)-induced proliferation of lung fibroblasts and production of chemokines in mesangial cells could be inhibited by lipoxin A(4) (LXA(4)). It is speculated that LXA(4) could modulate the CTGF-induced epithelial to mesenchymal transition.

Methods: The expressions of alpha-smooth muscle actin (alpha-SMA), E-cadherin, integrin-linked kinase (ILK), extracellular signal-regulated kinase 1/2 (ERK1/2), phosphatidylinositol 3-kinase (PI3-K), Akt and Smad signaling were assessed by Western blot and/or real-time RT-PCR, and activation of Ras or ILK by activity assay, expressions of alpha-SMA and zonula occludens-1 by immunofluorescence assay in proximal tubular epithelial cells (HK-2).

Results: Pretreatment of HK-2 cells with LXA(4) inhibited the morphological fibroblast-like changes and alpha-SMA expression induced by CTGF but not by transforming growth factor-beta(1) (TGF-beta(1)). The expressions of E-cadherin and zonula occludens-1 reduced by CTGF but not by TGF-beta(1) were increased by LXA(4). LXA(4) inhibited the expression and activity of ILK and activation of Ras, ERK1/2, PI3-K and Akt in HK-2 cells stimulated by CTGF. LXA(4) did not affect TGF-beta(1)-induced expression of ILK, Smad-2/3 phosphorylation and Smad-2's binding to Smad-4 and subsequent nuclear translocation.

Conclusion: LXA(4) inhibits the tubular epithelial to mesenchymal transition, initiated by CTGF but not by TGF-beta(1), via downregulation of ILK, Ras/MEK/ERK1/2 and PI3-K/Akt-dependent signal pathway stimulated by CTGF.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line
  • Connective Tissue Growth Factor / metabolism
  • Down-Regulation
  • Epithelial Cells / cytology
  • Epithelial Cells / drug effects
  • Epithelial-Mesenchymal Transition / drug effects*
  • Epithelial-Mesenchymal Transition / physiology
  • Humans
  • Kidney Tubules, Proximal / cytology*
  • Lipoxins / metabolism*
  • Lipoxins / pharmacology*
  • Protein Serine-Threonine Kinases / metabolism
  • Receptors, Formyl Peptide / genetics
  • Receptors, Formyl Peptide / metabolism*
  • Receptors, Lipoxin / genetics
  • Receptors, Lipoxin / metabolism*
  • Signal Transduction / drug effects
  • Transforming Growth Factor beta1 / metabolism
  • ras Proteins / blood
  • ras Proteins / metabolism

Substances

  • FPR2 protein, human
  • Lipoxins
  • Receptors, Formyl Peptide
  • Receptors, Lipoxin
  • Transforming Growth Factor beta1
  • lipoxin A4
  • Connective Tissue Growth Factor
  • Protein Serine-Threonine Kinases
  • ras Proteins