Developmental expression of parvalbumin mRNA in the cerebral cortex and hippocampus of the rat

Brain Res Mol Brain Res. 1995 Aug;32(1):1-13. doi: 10.1016/0169-328x(95)00056-x.

Abstract

Parvalbumin (PARV) belongs to the family of calcium-binding proteins bearing the EF hand domain. Immunocytochemical studies in the cerebral cortex have demonstrated that neurons containing PARV include two types of GABAergic interneurons, namely, basket and axo-axonic chandelier cells. The present study examines the onset and pattern of PARV mRNA expression during the development of rat neocortex and hippocampus by means of 'in situ' hybridization with an oligonucleotide probe corresponding to rat PARV cDNA. In animals aged P0-P6 no signal was detected above background in neocortex or hippocampus. At P8, a few cortical cells displayed a number of silver grains just above background levels. By P10 PARV mRNA-expressing cells in the neocortex were detected almost exclusively in layer V of somatosensory, frontal and cingulate cortices. At P12 PARV mRNA was mainly detected in layers IV, V and VIa. By P14 there was a marked overall increase in the entire neocortex, including layer II-III, both in the number of cells and in their intensity of labelling. Further maturation in the pattern of PARV mRNA concentration was observed between P16 and P21. In the hippocampus low hybridization was observed at P10-P12. In subsequent stages both the number of positive cells and the intensity of labelling increased steadily. No clear-cut radial gradients for the expression of PARV mRNA were observed in the hippocampal region. Our results show that the developmental radial gradient followed by PARV mRNA expression in the neocortex does not follow an 'inside-out' gradient, consistent with previous immunocytochemical findings. Taken together, these data indicate that the developmental sequence followed by the PARV protein directly reflects mRNA abundance and suggest that PARV mRNA expression correlates with the functional maturation of cortical interneurons.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Cerebral Cortex / growth & development
  • Cerebral Cortex / metabolism*
  • Gene Expression Regulation, Developmental / physiology*
  • Hippocampus / growth & development
  • Hippocampus / metabolism*
  • In Situ Hybridization
  • Molecular Sequence Data
  • Oligonucleotide Probes
  • Parvalbumins / genetics*
  • RNA, Messenger / biosynthesis*
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Oligonucleotide Probes
  • Parvalbumins
  • RNA, Messenger