Cajal–Retzius cells switch from expressing γ‐less to γ‐containing GABA A receptors during corticogenesis

Cajal–Retzius cells are implicated in regulating neuronal migration and lamination during corticogenesis. In rodents, Cajal–Retzius cells are transient, being prevalent in the marginal zone of the embryonic neocortex and declining over the first two postnatal weeks. While studies have examined in postnatal neocortex the properties of GABA A receptors in Cajal–Retzius cells, less is known about their disposition at embryonic stages. Here, we combined patch‐clamp electrophysiology and single‐cell mRNA profiling to probe the expression of GABA A receptors in Cajal–Retzius cells. In embryonic neocortical slices, GABA elicited GABA A receptor‐mediated current responses that were diazepam‐insensitive and inhibited by Zn 2+ , a pharmacological profile consistent with expression of γ‐less GABA A receptor isoforms. Non‐Cajal–Retzius cells in the same embryonic slices, on the other hand, were robustly potentiated by diazepam and were insensitive to Zn 2+ , typical of γ‐containing GABA A receptor isoforms, as were Cajal–Retzius cells in the postnatal neocortex. Single‐cell mRNA profiling and immunohistochemistry confirmed expression of GABA A receptor γ subunit transcript and protein, respectively, in individual reelin‐expressing cells in the postnatal cortex but not in their embryonic counterparts. We conclude that Cajal–Retzius cells express γ‐less GABA A receptors at embryonic stages and switch to expressing γ‐containing GABA A receptor isoforms during postnatal neocortical development.