Calcium oxalate monohydrate crystals stimulate monocyte chemoattractant protein-1 and transforming growth factor β1 expression in human renal epithelial cells

Mol Med Rep. 2012 May;5(5):1241-4. doi: 10.3892/mmr.2012.813. Epub 2012 Feb 28.

Abstract

Crystal-cell interactions play a key role in the formation of kidney stones. Few studies have referred to the role of monocyte chemoattractant protein-1 (MCP-1) and transforming growth factor β1 (TGFβ1) in kidney stone formation. Recently, a genome-wide analysis of genes related to kidney stone formation and eliminiation in mice indicated that MCP-1 and TGFβ1 are involved in nephrolithiasis. In this study, in order to verify whether MCP-1 and TGFβ1 are involved in the process of crystal-cell interactions in vitro, we observed the effects of calcium oxalate monohydrate (COM) on MCP-1 and TGFβ1 expression in cultured HK-2 cells. HK-2 cells were treated with different concentrations of COM, and a group of untreated cells served as the control. The expression of MCP-1 and TGFβ1 was detected by western blot analysis after treatments with different COM concentrations (300, 500, 700 and 900 µg/ml) for different times (3, 6, 12 and 24 h). We found that the expression of MCP-1 was upregulated by COM treatment in a dose-dependent manner, and was increased initially at the first 6 h of treatment, then slightly decreased over time. Also, COM treatment resulted in a dose-dependent increase in TGFβ1 expression, and the expression levels peaked at 12 h. This study demonstrates that COM stimulates the expression of MCP-1 and TGFβ1 in renal epithelial cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcium Oxalate / pharmacology*
  • Cell Line
  • Chemokine CCL2 / biosynthesis*
  • Dose-Response Relationship, Drug
  • Epithelial Cells / metabolism*
  • Epithelial Cells / pathology
  • Humans
  • Kidney / metabolism*
  • Kidney / pathology
  • Mice
  • Nephrolithiasis / metabolism
  • Nephrolithiasis / pathology
  • Time Factors
  • Transforming Growth Factor beta1 / biosynthesis*
  • Up-Regulation / drug effects*

Substances

  • CCL2 protein, human
  • Chemokine CCL2
  • Transforming Growth Factor beta1
  • Calcium Oxalate