Nerve growth factor signaling involves interaction between the Trk A receptor and lysophosphatidate receptor 1 systems: nuclear translocation of the lysophosphatidate receptor 1 and Trk A receptors in pheochromocytoma 12 cells

Noreen Akhtar Moughal, Catherine Waters, Balwinder Sambi, Susan Pyne, Nigel J Pyne

Research output: Contribution to journalArticle

65 Citations (Scopus)

Abstract

We report here that the nerve growth factor (NGF) and lysophosphatidate (LPA) receptor signaling systems interact to regulate the p42/p44 MAPK pathway in PC12 cells. This is based upon several lines of evidence. First, the treatment of PC12 cells, which express LPA(1) receptors, with a sub-maximal concentration of LPA and NGF induced synergistic activation of p42/p44 MAPK. Second, the transfection of PC12 cells with LPA(1) receptor anti-sense construct, which reduced the expression of LPA(1), abrogated both LPA- and NGF-stimulated activation of p42/p44 MAPK. Third, the over-expression of recombinant LPA(1) receptor potentiated LPA- and NGF-dependent activation of p42/p44 MAPK. Fourth, the over-expression of C-terminal GRK2 peptide (which sequesters G-protein betagamma subunits) or beta-arrestin I clathrin binding domain (amino acids: 319-418) or pre-treatment of cells with pertussis toxin reduced the LPA- and NGF-dependent stimulation of p42/p44 MAPK. These findings support a model in which the Trk A receptor uses a G-protein-mediated mechanism to regulate the p42/p44 MAPK pathway. Such G-protein-mediated signaling is activated by the LPA(1) receptor as a means of cross-talk regulation with the Trk A receptor. Fifth, the treatment of cells with LPA induced the transactivation of the Trk A receptor. Sixth, LPA and/or NGF stimulated the translocation of tyrosine phosphorylated Trk A receptor and LPA(1) receptor to the nucleus. Taken together, these findings suggest that NGF and LPA exert cross-talk regulation both at the level of p42/p44 MAPK signaling and in the nuclear translocation of LPA(1) and Trk A receptors.
Original languageEnglish
Pages (from-to)127-136
Number of pages10
JournalCellular Signalling
Volume16
Issue number1
Early online date14 Oct 2003
DOIs
Publication statusPublished - Jan 2004

Keywords

  • active transport, cell nucleus
  • animals
  • cell nucleus
  • drug synergism
  • lysophospholipids
  • MAP kinase signaling system
  • mitogen-activated protein kinase 1
  • mitogen-activated protein kinase 3
  • mitogen-activated protein kinases
  • nerve growth factor
  • PC12 cells
  • peptide fragments
  • rats
  • receptor, trkA
  • receptors, G-protein-coupled
  • receptors, lysophosphatidic acid
  • recombinant fusion proteins
  • transfection

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