PDGF-C and -D and their receptors PDGFR-alpha and PDGFR-beta in atherosclerotic human arteries

Eur J Clin Invest. 2009 Apr;39(4):320-7. doi: 10.1111/j.1365-2362.2009.02095.x.

Abstract

Background: Platelet derived growth factors (PDGFs) are mitogens for fibroblasts and smooth muscle cells. This growth factor family contains four members PDGF-A, PDGF-B, PDGF-C and PDGF-D. Biology of recently discovered PDGF-C and PDGF-D is not well-established. Here we studied the expression of PDGF-C and PDGF-D and their receptors PDGFR-alpha and PDGFR-beta in normal and atherosclerotic human arteries.

Materials and methods: Human arterial samples from amputations and autopsies were classified according to the atherosclerotic stage and the expression of PDGF-C and PDGF-D proteins and their receptors was studied by immunohistochemistry. In situ hybridization and reverse transcriptase-PCR were used to study mRNA expression.

Results: Both growth factors were expressed in medial smooth muscle cells (SMCs) in normal arteries and atherosclerotic lesions. However, clear differences were found in the expression profiles in endothelium: PDGF-C was strongly expressed in endothelial cells in both normal arteries and lesions whereas PDGF-D was only weakly expressed in endothelium. PDGF-C expression was very prominent in lesion macrophages. PDGF-D was expressed throughout the artery wall in lesions. PDGFR-alpha expression was strong in endothelium and in lesion macrophage-rich areas, whereas PDGFR-beta was mostly expressed in SMCs.

Conclusions: Our results suggest that PDGF-C may play an important role in endothelium in normal and atherosclerotic arteries and in macrophages in lesions. PDGF-D was expressed in all types of lesions with the same intensity and thus differs from the expression of PDGF-C.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Arteries / metabolism
  • Arteries / pathology
  • Atherosclerosis / immunology
  • Atherosclerosis / metabolism*
  • Atherosclerosis / pathology
  • Female
  • Humans
  • Immunohistochemistry / methods
  • Male
  • Middle Aged
  • Platelet-Derived Growth Factor / immunology
  • Platelet-Derived Growth Factor / metabolism*
  • RNA, Messenger / metabolism*
  • Receptor, Platelet-Derived Growth Factor alpha / immunology
  • Receptor, Platelet-Derived Growth Factor alpha / metabolism*
  • Receptor, Platelet-Derived Growth Factor beta / immunology
  • Receptor, Platelet-Derived Growth Factor beta / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction / methods

Substances

  • Platelet-Derived Growth Factor
  • RNA, Messenger
  • Receptor, Platelet-Derived Growth Factor alpha
  • Receptor, Platelet-Derived Growth Factor beta