Skip to content

Htr2a gene and 5-HT2A receptor expression in the cerebral cortex studied using genetically modified mice

Weber

Frontiers in Neuroscience 2010 DOI: 10.3389/fnins.2010.00036 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Observational study using transgenic and knockout mice Peer reviewed
Population Genetically modified mice
Topics Serotonin
Keywords Parvalbumin Gabaergic Cortex anatomy Receptor Pyramidal cell Neocortex Cerebral cortex Cell biology Hippocampus Inhibitory postsynaptic potential Genetics
Citations 201
Key findings 5-HT(2A) receptors are expressed in three main cortical neuronal populations: layer V pyramidal cells, GABAergic interneurons of middle layers, and subplate/Layer VIb non-pyramidal cells, with most GABAergic interneurons being parvalbumin-expressing fast-spiking cells depolarized by serotonin.

Abstract

Serotonin receptors of the 5-HT(2A) subtype are robustly expressed in the cerebral cortex where they have been implicated in the pathophysiology and therapeutics of mental disorders and the actions of hallucinogens. Much less is known, however, about the specific cell types expressing 5-HT(2A) receptors in cortex. In the current study we use immunohistochemical and electrophysiological approaches in genetically modified mice to address the expression of the Htr2a gene and 5-HT(2A) receptors in cortex. We first use an EGFP-expressing BAC transgenic mice and identify three main Htr2A gene expressing neuronal populations in cortex. The largest of these cell populations corresponds to layer V pyramidal cells of the anterior cortex, followed by GABAergic interneurons of the middle layers, and non-pyramidal cells of the subplate/Layer VIb. We then use 5-HT(2A) receptor knockout mice to identify an antibody capable of localizing 5-HT(2A) receptors in brain and use it to map these receptors. We find strong laminar expression of 5-HT(2A) receptors in cortex, especially along a diffuse band overlaying layer Va. This band exhibits a strong anteroposterior gradient that closely matches the localization of Htr2A expressing pyramidal cells of layer V. Finally we use electrophysiological and immunohistochemical approaches to show that most, but not all, GABAergic interneurons of the middle layers are parvalbumin expressing Fast-spiking interneurons and that these cells are depolarized and excited by serotonin, most likely through the activation of 5-HT(2A) receptors. These results clarify and extend our understanding of the cellular distribution of 5-HT(2A) receptors in the cerebral cortex.