Abstract
Cajal–Retzius cells are reelin-secreting neurons found in the marginal zone of the mammalian cortex during development. Recently, it has been proposed that Cajal–Retzius cells may be generated both early and late in corticogenesis, and may migrate into the cortex from proliferative zones in the subpallium (lateral ganglionic eminence and medial ganglionic eminence) or cortical hem. In the present study, we used reelin as a marker to study the properties of Cajal–Retzius cells, including their likely origins, neurotransmitters, and birthdates. In double labeling experiments, Cajal–Retzius cells (reelin +) expressed transcription factors characteristic of pallial neurons (Tbr1 and Emx2), contained high levels of glutamate, were usually calretinin +, and were born early in corticogenesis, on embryonic days (E)10.5 and E11.5. Tbr1 + cells in the marginal zone were almost always reelin +. The first Cajal–Retzius cells (Tbr1 +/reelin +) appeared in the preplate on E10.5. In contrast, interneurons expressed a subpallial transcription factor (Dlx), contained high levels of GABA, were frequently calbindin +, and were born throughout corticogenesis (from E10.5 to E16.5). Interneurons (Dlx +) first appeared in the cortex on E12.5. Our results suggest that the marginal zone contains two main types of neurons: Cajal–Retzius cells derived from the pallium, and migrating interneurons derived from the subpallium.
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