Phenotypic characterization of septal neurons in culture: immunohistochemistry of GABA, calbindin D-28k and choline acetyltransferase, and histochemistry of acetylcholinesterase

Brain Res Dev Brain Res. 1998 Jan 14;105(1):1-8.

Abstract

Phenotypes of septal neurons, dissociated from 19-day-old fetal rat brains and then cultured in a medium containing nerve growth factor for 4 weeks, were examined using gamma-aminobutyric acid (GABA), calbindin D-28k, parvalbumin and choline acetyltransferase immunohistochemistry, and acetylcholinesterase histochemistry. There were primarily four groups of neurons identified in this septal culture: the first group (12.7% of 212 neurons examined) displayed a cholinergic, but not GABAergic, phenotype and had an average diameter of 13.6 +/- 2.7 microm (mean +/- S.D.); the second group (31.6%) displayed both cholinergic and GABAergic phenotypes and had a diameter of 12.2 +/- 2.8 microm; the third group (31.0%) displayed only a GABAergic phenotype and had a diameter of 10.4 +/- 2.3 microm; and the fourth group (24.7%) displayed neither a GABAergic nor cholinergic phenotype and had a diameter of 10.4 +/- 2.1 microm. Neurons in the first two groups described were significantly larger than those in the second two groups; neurons in the third and fourth groups were the same size. Calbindin D-28k was expressed in some neurons of each group (31.3%, 18.8%, 9.6% and 15.7%, respectively). These results demonstrate that septal neurons have the ability to express a variety of phenotypes when grown in vitro. This culture will be a useful tool for studying mechanisms of phenotype expression in septal neurons.

MeSH terms

  • Acetylcholinesterase / metabolism*
  • Animals
  • Calbindins
  • Cells, Cultured
  • Choline O-Acetyltransferase / metabolism*
  • Female
  • Immunohistochemistry
  • Nerve Tissue Proteins / metabolism*
  • Neurons / enzymology
  • Neurons / metabolism*
  • Parvalbumins / metabolism
  • Phenotype
  • Rats
  • S100 Calcium Binding Protein G / metabolism*
  • gamma-Aminobutyric Acid / metabolism*

Substances

  • Calbindins
  • Nerve Tissue Proteins
  • Parvalbumins
  • S100 Calcium Binding Protein G
  • gamma-Aminobutyric Acid
  • Choline O-Acetyltransferase
  • Acetylcholinesterase