IHG-1 amplifies TGF-beta1 signaling and is increased in renal fibrosis

J Am Soc Nephrol. 2008 Sep;19(9):1672-80. doi: 10.1681/ASN.2007101080. Epub 2008 May 28.

Abstract

Induced in high glucose-1 (IHG-1) is an evolutionarily conserved gene transcript upregulated by high extracellular glucose concentrations, but its function is unknown. Here, it is reported that the abundance of IHG-1 mRNA is nearly 10-fold higher in microdissected, tubule-rich renal biopsies from patients with diabetic nephropathy compared with control subjects. In the diabetic nephropathy specimens, in situ hybridization localized IHG-1 to tubular epithelial cells along with TGF-beta1 and activated Smad3, suggesting a possible role in the development of tubulointerstitial fibrosis. Supporting this possibility, IHG-1 mRNA and protein expression also increased with unilateral ureteral obstruction. In the HK-2 proximal tubule cell line, overexpression of IHG-1 increased TGF-beta1-stimulated expression of connective tissue growth factor and fibronectin. IHG-1 was found to amplify TGF-beta1-mediated transcriptional activity by increasing and prolonging phosphorylation of Smad3. Conversely, inhibition of endogenous IHG-1 with small interference RNA suppressed transcriptional responses to TGF-beta1. In summary, IHG-1, which increases in diabetic nephropathy, may enhance the actions of TGF-beta1 and contribute to the development of tubulointerstitial fibrosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Cell Line
  • Connective Tissue Growth Factor
  • Conserved Sequence
  • Diabetic Nephropathies / metabolism*
  • Extracellular Fluid / metabolism
  • Fibronectins / metabolism
  • Fibrosis
  • Glucose / metabolism
  • Humans
  • Immediate-Early Proteins / metabolism
  • Intercellular Signaling Peptides and Proteins / metabolism
  • Kidney Tubules / metabolism*
  • Kidney Tubules / pathology
  • Molecular Sequence Data
  • Phosphorylation
  • Proteins / genetics
  • Proteins / metabolism*
  • Sequence Alignment
  • Signal Transduction
  • Smad3 Protein / metabolism
  • Transforming Growth Factor beta1 / metabolism*
  • Ureteral Obstruction / metabolism*

Substances

  • CCN2 protein, human
  • Fibronectins
  • Immediate-Early Proteins
  • Intercellular Signaling Peptides and Proteins
  • Proteins
  • SMAD3 protein, human
  • Smad3 Protein
  • THG1L protein, human
  • Transforming Growth Factor beta1
  • Connective Tissue Growth Factor
  • Glucose