GABA and glutamate depolarize cortical progenitor cells and inhibit DNA synthesis

TLDR

In the ventricular zone, glutamate signals through AMPA/kainate receptors and GABA signals through GABAA receptors. The study shows that GABA and glutamate depolarize ventricular‑zone progenitors, raise intracellular Ca²⁺, and suppress DNA synthesis, while blocking their receptors restores DNA synthesis, revealing a novel role for these neurotransmitters in regulating cortical neurogenesis.

Abstract

We have found that, during the early stages of cortical neurogenesis, both GABA and glutamate depolarize cells in the ventricular zone of rat embryonic neocortex. In the ventricular zone, glutamate acts on AMPA/kainate receptors, while GABA acts on GABAA receptors. GABA induces an inward current at resting membrane potentials, presumably owing to a high intracellular Cl- concentration maintained by furosemide-sensitive Cl- transport. GABA and glutamate also produce increases in intracellular Ca2+ in ventricular zone cells, in part through activation of voltage-gated Ca2+ channels. Furthermore, GABA and glutamate decrease the number of embryonic cortical cells synthesizing DNA. Depolarization with K+ similarly decreases DNA synthesis, suggesting that the neurotransmitters act via membrane depolarization. Applied alone, GABAA and AMPA/kainate receptor antagonists increase DNA synthesis, indicating that endogenously released amino acids influence neocortical progenitors in the cell cycle. These results demonstrate a novel role for amino acid neurotransmitters in regulating neocortical neurogenesis.