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Proceedings of the National Academy of Sciences - PNAS, 2015-09, Vol.112 (36), p.E5058-E5067
2015
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Autor(en) / Beteiligte
Titel
Subset of early radial glial progenitors that contribute to the development of callosal neurons is absent from avian brain
Ist Teil von
  • Proceedings of the National Academy of Sciences - PNAS, 2015-09, Vol.112 (36), p.E5058-E5067
Ort / Verlag
United States: National Academy of Sciences
Erscheinungsjahr
2015
Quelle
EZB-FREE-00999 freely available EZB journals
Beschreibungen/Notizen
  • The classical view of mammalian cortical development suggests that pyramidal neurons are generated in a temporal sequence, with all radial glial cells (RGCs) contributing to both lower and upper neocortical layers. A recent opposing proposal suggests there is a subgroup of fate-restricted RGCs in the early neocortex, which generates only upper-layer neurons. Little is known about the existence of fate restriction of homologous progenitors in other vertebrate species. We investigated the lineage of selected Emx2⁺ [vertebrate homeobox gene related toDrosophila empty spiracles(ems)] RGCs in mouse neocortex and chick forebrain and found evidence for both sequential and fate-restricted programs only in mouse, indicating that these complementary populations coexist in the developing mammalian but not avian brain. Among a large population of sequentially programmed RGCs in the mouse brain, a subset of self-renewing progenitors lack neurogenic potential during the earliest phase of corticogenesis. After a considerable delay, these progenitors generate callosal upper-layer neurons and glia. On the other hand, we found no homologous delayed population in any sectors of the chick forebrain. This finding suggests that neurogenic delay of selected RGCs may be unique to mammals and possibly associated with the evolution of the corpus callosum.

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