Inhibition of integrin-linked kinase via a siRNA expression plasmid attenuates connective tissue growth factor-induced human proximal tubular epithelial cells to mesenchymal transition

Am J Nephrol. 2008;28(1):143-51. doi: 10.1159/000110019. Epub 2007 Oct 19.

Abstract

Background: Increasing evidence suggests that connective tissue growth factor (CTGF) is involved in the epithelial-to-mesenchymal transition (EMT). The exact intracellular events that drive this process, however, are not fully understood. In this study, we investigated the role of integrin-linked kinase (ILK) in mediating CTGF-induced EMT.

Methods: The expression of alpha-smooth muscle actin (alpha-SMA) and E-cadherin upon the stimulation by recombinant human CTGF (rhCTGF) in cultured human tubular epithelial cell line (HK-2) was detected by real-time RT-PCR and Western blot. Subsequently, the role of ILK was determined by using ILK siRNA.

Results: rhCTGF increased the mRNA expression of alpha-SMA significantly in a dose- and time-dependent manner, while E-cadherin mRNA decreased in a dose- and time-dependent manner. alpha-SMA protein was up-regulated after stimulation by 5 ng/ml CTGF for 96 h, and increased further after stimulation by 50 ng/ml. An immunocytochemical study showed that alpha-SMA was initially detectable at 48 h, and increased further at 72 h, while there was almost no alpha-SMA immunostaining observed in the control group at the same time point. E-cadherin protein was also down-regulated in a dose-dependent manner. Transfection of HK-2 cells with ILK-siRNA significantly attenuated rhCTGF-induced alpha-SMA induction and E-cadherin repression.

Conclusion: Our study suggested that ILK mediated the effect of EMT in proximal tubular epithelial cells stimulated by CTGF.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / genetics
  • Actins / metabolism
  • Cadherins / genetics
  • Cadherins / metabolism
  • Cell Line, Transformed
  • Connective Tissue Growth Factor
  • Epithelial Cells / cytology
  • Epithelial Cells / physiology
  • Humans
  • Immediate-Early Proteins / metabolism*
  • Immediate-Early Proteins / pharmacology
  • Intercellular Signaling Peptides and Proteins / metabolism*
  • Intercellular Signaling Peptides and Proteins / pharmacology
  • Kidney Tubules, Proximal / cytology
  • Kidney Tubules, Proximal / physiology*
  • Mesoderm / cytology
  • Nephritis, Interstitial / pathology*
  • Nephritis, Interstitial / physiopathology
  • Plasmids
  • Protein Serine-Threonine Kinases / genetics*
  • Protein Serine-Threonine Kinases / metabolism
  • RNA, Messenger / metabolism
  • RNA, Small Interfering / pharmacology*
  • Recombinant Proteins / metabolism
  • Recombinant Proteins / pharmacology
  • Transfection

Substances

  • Actins
  • CCN2 protein, human
  • Cadherins
  • Immediate-Early Proteins
  • Intercellular Signaling Peptides and Proteins
  • RNA, Messenger
  • RNA, Small Interfering
  • Recombinant Proteins
  • Connective Tissue Growth Factor
  • integrin-linked kinase
  • Protein Serine-Threonine Kinases