Growth factor and procollagen type I gene expression in human liver disease

Gastroenterology. 1995 Jan;108(1):145-56. doi: 10.1016/0016-5085(95)90019-5.

Abstract

Background/aims: Growth factors have been implicated in the pathogenesis of liver fibrosis, a major determinant of the clinical course of chronic liver disease. The aim of this study was to study the relationship of growth factor expression to inflammation and fibrosis in a variety of human liver diseases.

Methods: We studied by in situ hybridization the expression of transforming growth factor (TGF) beta 1, platelet-derived growth factor (PDGF) A and PDGF-B, and procollagen type I (pro-I) messenger RNAs (mRNAs) in liver diseases of various etiologies.

Results: Pro-I mRNA was expressed by mesenchymal cells at sites of inflammation and scarring, where TGF-beta 1 immunoreactivity was often found, and by perisinusoidal cells. TGF-beta 1 and PDGF-A mRNAs were expressed mainly by mononuclear cells and proliferating ductular cells. TGF-beta 1 mRNA was also expressed by perisinusoidal cells. PDGF-A gene expression was more common than that of PDGF-B. Pro-I and TGF-beta 1 expression correlated with both ductular proliferation and tissue inflammation, whereas PDGF-A and PDGF-B only correlated with ductular proliferation.

Conclusions: Our data suggest that TGF-beta 1 and PDGF are involved in human liver inflammation and fibrosis. The expression of growth factor mRNAs in proliferating ductular cells may indicate a role for these cells in liver fibrogenesis and may help explain the pathophysiology of conditions such as biliary atresia progressing to fibrosis despite the absence of marked inflammation.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Gene Expression*
  • Growth Substances / genetics*
  • Growth Substances / metabolism
  • Humans
  • Immunohistochemistry
  • In Situ Hybridization
  • Liver / metabolism
  • Liver Diseases / genetics*
  • Liver Diseases / pathology
  • Platelet-Derived Growth Factor / genetics
  • Procollagen / genetics*
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins c-sis
  • RNA, Messenger / metabolism
  • Reference Values
  • Transforming Growth Factor beta / genetics

Substances

  • Growth Substances
  • Platelet-Derived Growth Factor
  • Procollagen
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-sis
  • RNA, Messenger
  • Transforming Growth Factor beta
  • platelet-derived growth factor A