Effect of Brn-3a deficiency on CGRP-immunoreactivity in the dorsal root ganglion

Neuroreport. 2002 Mar 25;13(4):409-12. doi: 10.1097/00001756-200203250-00009.

Abstract

Immunohistochemistry for calcitonin gene-related peptide (CGRP) was performed on the dorsal root ganglion (DRG) and spinal cord in wildtype and knockout mice for Brn-3a. CGRP-immunoreactive (-IR) neurons were abundant in the DRG of wildtype, heterozygous and knockout mice. Cell size analysis revealed that CGRP-IR neurons were of various sizes in wildtype and heterozygous mice. In the knockout mice, however, most of CGRP-IR neurons were small. In the spinal cord of knockout mice, the number of CGRP-IR fibers increased in the dorsal column but decreased in the deep part of the dorsal horn. The loss of Brn-3a may have different effects on CGRP-IR expression in small and large DRG neurons.

MeSH terms

  • Animals
  • Calcitonin Gene-Related Peptide / analysis*
  • Calcitonin Gene-Related Peptide / biosynthesis
  • Calcitonin Gene-Related Peptide / genetics
  • DNA-Binding Proteins / deficiency*
  • DNA-Binding Proteins / genetics*
  • Ganglia, Spinal / chemistry*
  • Ganglia, Spinal / cytology
  • Ganglia, Spinal / metabolism
  • Immunohistochemistry / methods
  • Mice
  • Mice, Knockout
  • Mice, Mutant Strains
  • Spinal Cord / chemistry
  • Spinal Cord / cytology
  • Spinal Cord / metabolism
  • Transcription Factor Brn-3
  • Transcription Factor Brn-3A
  • Transcription Factors / deficiency*
  • Transcription Factors / genetics*

Substances

  • DNA-Binding Proteins
  • Pou4f1 protein, mouse
  • Transcription Factor Brn-3
  • Transcription Factor Brn-3A
  • Transcription Factors
  • Calcitonin Gene-Related Peptide