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Cell Stem Cell ; 23(1): 60-73.e6, 2018 Jul 05.
Article in English | MEDLINE | ID: mdl-29937203

ABSTRACT

Cortical deep projection neurons (DPNs) are implicated in neurodevelopmental disorders. Although recent findings emphasize post-mitotic programs in projection neuron fate selection, the establishment of primate DPN identity during layer formation is not well understood. The subplate lies underneath the developing cortex and is a post-mitotic compartment that is transiently and disproportionately enlarged in primates in the second trimester. The evolutionary significance of subplate expansion, the molecular identity of its neurons, and its contribution to primate corticogenesis remain open questions. By modeling subplate formation with human pluripotent stem cells (hPSCs), we show that all classes of cortical DPNs can be specified from subplate neurons (SPNs). Post-mitotic WNT signaling regulates DPN class selection, and DPNs in the caudal fetal cortex appear to exclusively derive from SPNs. Our findings indicate that SPNs have evolved in primates as an important source of DPNs that contribute to cortical lamination prior to their known role in circuit formation.


Subject(s)
Cell Differentiation , Cell Lineage , Models, Biological , Neurons/cytology , Pluripotent Stem Cells/cytology , Animals , Cells, Cultured , Humans , Mice , Mice, Inbred C57BL , Neurons/metabolism , Pluripotent Stem Cells/metabolism
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