The interdependence of EGF-R and SGK-1 in fibronectin expression in primary kidney cortical fibroblast cells

Int J Biochem Cell Biol. 2007;39(5):1047-54. doi: 10.1016/j.biocel.2007.02.013. Epub 2007 Feb 23.

Abstract

Background: Epidermal growth factor (EGF) has been shown to play a role in the nephromegaly and enhanced sodium reabsorption observed in diabetic nephropathy. This is recognized to be dependent on activation of serine threonine glucocorticoid kinase-1 (SGK-1). However, the roles of EGF and SGK-1 in renal fibrogenesis observed under high glucose conditions have not been established.

Methods: Primary cultures of human cortical fibroblasts (CFs) were used as the model in which to study the dependent and independent effects of high glucose, EGF and SGK-1 on the expression of the extracellular matrix protein (ECM) fibronectin. Wild type CFs expressing SGK-1, or cells in which SGK-1 was effectively silenced using siRNA methodology, were exposed to normal (5mM) or high (25mM) glucose, or EGF (10ng/ml) for 48hr and fibronectin assessed. The role of the EGF-receptor and its relationship to SGK-1 signaling was studied using concurrent treatment with PKI166, a specific inhibitor of EGF-receptor.

Results: Exposure of CF to high glucose and EGF increased phosphorylated EGF-R, SGK-1, and fibronectin expression in wild-type cells. Inhibition of the EGF-R reduced SGK-1 and fibronectin expression in control, and following exposure to EGF and high glucose conditions. In cells in which SGK-1 was silenced, fibronectin was reduced and there was no significant increase in pEGF-R, suggesting that SGK-1 is downstream of the EGF-R and negatively inhibits EGF-R activation.

Conclusion: These results suggest that high glucose induced fibronectin expression is mediated through the EGF-R and downstream expression of SGK-1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blotting, Western
  • Cells, Cultured
  • Epidermal Growth Factor / pharmacology
  • ErbB Receptors / genetics
  • ErbB Receptors / metabolism*
  • Fibroblasts / cytology
  • Fibroblasts / drug effects
  • Fibroblasts / metabolism*
  • Fibronectins / genetics
  • Fibronectins / metabolism
  • Gene Expression / drug effects
  • Gene Silencing
  • Glucose / pharmacology
  • Humans
  • Immediate-Early Proteins / genetics
  • Immediate-Early Proteins / metabolism*
  • Kidney / cytology
  • Kidney / metabolism*
  • Phosphorylation / drug effects
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism*
  • RNA, Small Interfering / genetics
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • Fibronectins
  • Immediate-Early Proteins
  • RNA, Small Interfering
  • Epidermal Growth Factor
  • ErbB Receptors
  • Protein Serine-Threonine Kinases
  • serum-glucocorticoid regulated kinase
  • Glucose