RECEPTOR-BINDING OF PDGF-AA AND PDGF-BB, AND THE MODULATION OF PDGF RECEPTORS BY TGF-BETA, IN HUMAN PERIODONTAL-LIGAMENT CELLS


Oates T. W. , KÖSE K. N. , XIE J., GRAVES D. T. , Collins J. M. , Cochran D. L.

JOURNAL OF CELLULAR PHYSIOLOGY, cilt.162, sa.3, ss.359-366, 1995 (SCI İndekslerine Giren Dergi) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 162 Konu: 3
  • Basım Tarihi: 1995
  • Doi Numarası: 10.1002/jcp.1041620308
  • Dergi Adı: JOURNAL OF CELLULAR PHYSIOLOGY
  • Sayfa Sayıları: ss.359-366

Özet

The growth factors PDGF-AA and PDGF-BB have previously been shown to be potent mitogens for human periodontal ligament (hPDL) cells in vitro. Additionally, the mitogenic response to PDGF-AA has been shown to be specifically inhibited by TGF-beta. The purpose of the present investigation was to examine the binding of PDGF-AA and PDGF-BB, and the modulation of PDGF binding by TGF-beta, in hPDL cells. Scatchard analysis identified an average of 32,000 PDGF-AA high-affinity binding sites per cell with a dissociation constant (K-d) of 0.66 nM and an average of 36,000 PDCF-BB binding sites per cell with a dissociation constant (k(d)) of 0.44 nM. After treatment with TGF-beta, the receptor number for PDGF-AA was found to specifically decrease by approximately 50%, with no change in binding affinity. This reduced number of binding sites was shown to correlate with both a decrease in levels of receptor tyrosine phosphorylation and a decreased number of alpha receptor subunits. Northern blot analysis identified the TGF-P-mediated decrease in PDGF alpha receptor subunit mRNA levels. PDGF-BB showed little change in the number of binding sites or in the binding affinity with TGF-beta treatment, and the data were consistent with an increase in the number of beta receptor subunits. These results demonstrate nearly equivalent numbers of receptors for both PDGF-AA and PDGF-BB in hPDL cells. Also, modulation of PDGF binding, by TFG-beta, was shown to result in a reduced number of a receptor subunits with an increase in the number of beta receptor subunits. (C) 1995 Wiley-Liss, Inc.