Expression of connective tissue growth factor in human renal fibrosis

Kidney Int. 1998 Apr;53(4):853-61. doi: 10.1111/j.1523-1755.1998.00820.x.


Chronic renal failure may occur in etiologically diverse renal diseases and can be caused by hemodynamic, immunologic and metabolic factors. Initial damage may evoke irreversible scarring, which involves production of a number of proinflammatory and fibrogenic cytokines, including platelet-derived growth factor (PDGF) and transforming growth factor beta (TGF-beta). Connective tissue growth factor (CTGF), a cytokine of the family of growth regulators comprising sef10, cyr61, CTGF and nov, has recently been described in association with scleroderma and other scarring conditions. We investigated CTGF mRNA expression in 65 human renal biopsy specimens of various renal diseases by in situ hybridization. In control human kidney CTFG mRNA was mainly expressed in visceral epithelial cells, parietal epithelial cells, and some interstitial cells. Connective tissue growth factor was strongly up-regulated in the extracapillary and severe mesangial proliferative lesions of crescentic glomerulonephritis, IgA nephropathy, focal and segmental glomerulosclerosis and diabetic nephropathy. An increase in the number of cells expressing CTGF mRNA was observed at sites of chronic tubulointerstitial damage, which correlated with the degree of damage. in the tubulointerstitial area the majority of the CTGF mRNA positive cells coexpressed alpha-smooth muscle actin, and were negative for macrophage markers. Our results indicate that CTGF may be a common growth factor involved in renal fibrosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biopsy
  • Blotting, Northern
  • Connective Tissue Growth Factor
  • Fibrosis
  • Glomerular Mesangium / chemistry
  • Glomerular Mesangium / pathology
  • Growth Substances / analysis*
  • Growth Substances / genetics*
  • Humans
  • Immediate-Early Proteins*
  • In Situ Hybridization
  • Intercellular Signaling Peptides and Proteins*
  • Kidney Diseases / metabolism*
  • Kidney Diseases / pathology
  • Mitogens / analysis*
  • Mitogens / genetics*
  • Nephroblastoma Overexpressed Protein
  • RNA, Messenger / analysis
  • Sclerosis
  • Transcription, Genetic


  • CCN2 protein, human
  • CCN3 protein, human
  • Growth Substances
  • Immediate-Early Proteins
  • Intercellular Signaling Peptides and Proteins
  • Mitogens
  • Nephroblastoma Overexpressed Protein
  • RNA, Messenger
  • Connective Tissue Growth Factor