Duration and magnitude of nerve growth factor signaling depend on the ratio of p75LNTR to TrkA

J Neurosci Res. 1998 Feb 15;51(4):442-53. doi: 10.1002/(SICI)1097-4547(19980215)51:4<442::AID-JNR4>3.0.CO;2-C.


The role of the low affinity neurotrophin receptor p75LNTR in neurotrophin signal transduction remains open. Recent reports show that this receptor generates intracellular signals independent of Trk activity, and others imply that it collaborates with Trk(s) to enhance cellular responses to low neurotrophin concentrations. We have used the Cytosensor microphysiometer as a direct marker of intracellular metabolic activity to address the physiologic role of p75LNTR in nerve growth factor (NGF) signal transduction. NGF treatment of PC12 or TrkA-transfected Chinese hamster ovary (CHO) cells results in a rapid, transient increase in the extracellular acidification rate as measured by the Cytosensor; in both cell types, p75LNTR enhances this response. p75LNTR affects both the magnitude of and the duration of the extracellular acidification response to NGF. Moreover, it is not merely the presence of p75LNTR, but also the ratio of p75LNTR:TrkA which determines cellular responsiveness to NGF. In transiently transfected CHO cells, a 5:1 ratio of p75LNTR:trkA cDNAs produced the greatest change in NGF-induced acid secretion. Pretreatment of PC12 cells with anti-p75LNTR antibodies decreased the responsiveness to NGF. However, long-term NGF exposure to PC12 cells in which p75LNTR expression was decreased to approximately 10% of wild-type levels showed a longer duration of acid secretion compared to wild-type PC12 cells. Together, these data suggest that p75LNTR may play a dual role in modulating NGF signal transduction by enhancing and extending cellular responses to short-term ligand exposures while attenuating the metabolic response to long-term ligand exposures. With regard to potential Trk-independent p75LNTR signal transduction mechanisms, we detected no change in extracellular acidification response in 75LNTR-transfected CHO cells, PCNA-15 fibroblasts, or Schwann cells, all of which express large amounts of p75LNTR and no Trk. Thus, p75LNTR cannot produce any signal detected by microphysiometry in the absence of TrkA.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antibodies / pharmacology
  • CHO Cells
  • Cell Line
  • Cricetinae
  • DNA, Antisense / pharmacology
  • Extracellular Space / metabolism
  • Fibroblasts
  • Nerve Growth Factors / physiology*
  • PC12 Cells
  • Proto-Oncogene Proteins / physiology*
  • Rats
  • Receptor Protein-Tyrosine Kinases / physiology*
  • Receptor, Nerve Growth Factor
  • Receptor, trkA
  • Receptors, Nerve Growth Factor / immunology
  • Receptors, Nerve Growth Factor / physiology*
  • Schwann Cells
  • Signal Transduction* / genetics
  • Transfection


  • Antibodies
  • DNA, Antisense
  • Nerve Growth Factors
  • Proto-Oncogene Proteins
  • Receptor, Nerve Growth Factor
  • Receptors, Nerve Growth Factor
  • Receptor Protein-Tyrosine Kinases
  • Receptor, trkA