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Growth factors modulate junctional cell-to-cell communication
Authors:Pedro E. Maldonado  Birgit Rose  Werner R. Loewenstein
Affiliation:(1) Department of Physiology and Biophysics, University of Miami School of Medicine, 33101 Miami, Florida;(2) Present address: Department of Physiology, University of Pennsylvania School of Medicine, Philadelphia, PA
Abstract:Summary The epidermal growth factor (EGF) and the platelet-derived growth factor (PDGF) inhibit gap junctional communication in the mammalian cell lines NRK and BalbC 3T3: cell-to-cell transfer of a 400-dalton tracer molecule is reduced and junctional conductance is reduced. The inhibition of cell-to-cell transfer is reversible and dose dependent; half-maximal effects are obtained at 10–9 and 10–11m concentrations of EGF and PDGF, respectively. The response of junctional conductance is detectable within 2 min of EGF application and reaches a maximum within 10 min. It is among the earliest cellular responses to this growth factor and may be significant in the regulation of growth. The response is lacking in EGF receptor-deficient NIH 3T3 cells. The transforming factor beta (TGFbeta) enhances junctional communication in BalbC 3T3: cell-to-cell transfer is increased over a period of 8 hr. But in NRK cells, where it upregulates EGF receptors, TGFbeta reduces junctional communication synergistically with EGF.
Keywords:gap junction  growth factors  EGF  PDGF  TGF  /content/u77j08420ru35721/xxlarge946.gif"   alt="  beta"   align="  MIDDLE"   BORDER="  0"  >  cell-to-cell communication  junctional communication
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