Characterization of intracellular pathways leading to coinduction of thrombospondin-1 and TGF-beta1 expression in rat hepatic stellate cells

Growth Factors. 2005 Jun;23(2):77-85. doi: 10.1080/08977190500095980.

Abstract

Accumulating evidence has identified Thrombospondin (TSP)-1 as important activator of latent TGF-beta. Since little is known about signal transduction pathways regulating TSP expression in liver, we investigated cytokine-mediated upregulation of TSP-1 and TGF-beta1 in primary rat hepatic stellate cells (HSC). PDGF-BB and TNF-a rapidly coinduce mRNA levels of TSP-1 and TGF-beta1. Interestingly, blockade of basal Erk activity by synthetic Erk-binding peptides also leads to strong induction of both mRNA transcripts in non-stimulated cells. We show that PDGF-BB induces TSP-1 and TGF-beta1 via the src kinase pathway whereas TNF-a utilizes the MAPK/Erk pathway. However, especially TSP-1 induction by both cytokines involves a pathway, which depends to a certain extent on PI3 kinase activity. In summary the data illustrate specific pathways activated by PDGF-BB and TNF-a in HSC giving new insights into the tightly controlled mechanisms regulating TSP-1 and TGF-beta1 expression in these cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Becaplermin
  • Blotting, Northern
  • Blotting, Western
  • Cell Differentiation
  • Cell Line
  • Dose-Response Relationship, Drug
  • Enzyme Inhibitors / pharmacology
  • Gene Expression Regulation, Enzymologic*
  • Hepatocytes / metabolism*
  • Humans
  • Liver / metabolism*
  • MAP Kinase Signaling System
  • Models, Biological
  • Peptides / chemistry
  • Phosphorylation
  • Platelet-Derived Growth Factor / metabolism
  • Proto-Oncogene Proteins c-sis
  • RNA / metabolism
  • RNA, Messenger / metabolism
  • Rats
  • Signal Transduction
  • Thrombospondin 1 / metabolism*
  • Transforming Growth Factor beta / metabolism*
  • Tumor Necrosis Factor-alpha / metabolism
  • src-Family Kinases / metabolism

Substances

  • Enzyme Inhibitors
  • Peptides
  • Platelet-Derived Growth Factor
  • Proto-Oncogene Proteins c-sis
  • RNA, Messenger
  • Thrombospondin 1
  • Transforming Growth Factor beta
  • Tumor Necrosis Factor-alpha
  • Becaplermin
  • RNA
  • src-Family Kinases