trkC-like immunoreactivity in the primate descending serotoninergic system

Eur J Neurosci. 1994 Feb 1;6(2):230-6. doi: 10.1111/j.1460-9568.1994.tb00265.x.

Abstract

In the search for substances with a potential role in plastic responses of spinal motoneurons we have studied the distribution of trkC-like immunoreactivity in the spinal cord of adult monkeys (Macaca fascicularis). The presence of trkC, which is a signal-transducing receptor for neurotrophin-3, was detected by the use of indirect immunofluorescence with a rabbit polyclonal antibody raised against a synthetic peptide corresponding to the carboxy-terminal domain of the mouse trkC-encoded protein, thus detecting only full-length signal-transducing receptors. trkC-immunoreactive fibres/varicosities could be found at all spinal cord levels and the densest innervation was found in the autonomic intermediolateral and Onuf's nuclei, but somatic motoneuron pools also received a significant contribution of trkC-immunoreactive fibres. Terminals immunoreactive for trkC were also seen in the dorsal horn. Double-labelling experiments revealed a high degree of coexistence between trkC- and 5-hydroxytryptamine (serotonin)-like immunoreactivity in all areas except in the dorsal horn. The results of the present study suggest that neurotrophic signalling with an influence on serotoninergic as well as non-serotoninergic inputs to the adult monkey spinal cord is at hand.

Publication types

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

MeSH terms

  • Animals
  • Fluorescent Antibody Technique
  • Immunohistochemistry
  • Macaca fascicularis
  • Membrane Proteins / analysis
  • Membrane Proteins / biosynthesis
  • Motor Neurons / cytology
  • Motor Neurons / metabolism*
  • Organ Specificity
  • Proto-Oncogenes
  • Receptor Protein-Tyrosine Kinases / analysis*
  • Receptor Protein-Tyrosine Kinases / biosynthesis
  • Receptor, trkC
  • Receptors, Growth Factor / analysis*
  • Receptors, Growth Factor / biosynthesis
  • Serotonin / metabolism*
  • Spinal Cord / cytology
  • Spinal Cord / metabolism*

Substances

  • Membrane Proteins
  • Receptors, Growth Factor
  • Serotonin
  • Receptor Protein-Tyrosine Kinases
  • Receptor, trkC