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Differential Expression Levels of Sox9 in Early Neocortical Radial Glial Cells Regulate the Decision between Stem Cell Maintenance and Differentiation.
Fabra-Beser, Jaime; Alves Medeiros de Araujo, Jessica; Marques-Coelho, Diego; Goff, Loyal A; Costa, Marcos R; Müller, Ulrich; Gil-Sanz, Cristina.
Afiliación
  • Fabra-Beser J; BIOTECMED Institute, Universidad de Valencia, Burjassot, 46100 Valencia, Spain.
  • Alves Medeiros de Araujo J; The Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
  • Marques-Coelho D; Brain Institute, Federal University of Rio Grande do Norte, RN 59056-450, Natal, Brazil.
  • Goff LA; Brain Institute, Federal University of Rio Grande do Norte, RN 59056-450, Natal, Brazil.
  • Costa MR; Bioinformatics Multidisciplinary Environment, IMD, Federal University of Rio Grande do Norte, RN 59078-400, Natal, Brazil.
  • Müller U; The Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
  • Gil-Sanz C; Brain Institute, Federal University of Rio Grande do Norte, RN 59056-450, Natal, Brazil.
J Neurosci ; 41(33): 6969-6986, 2021 08 18.
Article en En | MEDLINE | ID: mdl-34266896
ABSTRACT
Radial glial progenitor cells (RGCs) in the dorsal telencephalon directly or indirectly produce excitatory projection neurons and macroglia of the neocortex. Recent evidence shows that the pool of RGCs is more heterogeneous than originally thought and that progenitor subpopulations can generate particular neuronal cell types. Using single-cell RNA sequencing, we have studied gene expression patterns of RGCs with different neurogenic behavior at early stages of cortical development. At this early age, some RGCs rapidly produce postmitotic neurons, whereas others self-renew and undergo neurogenic divisions at a later age. We have identified candidate genes that are differentially expressed among these early RGC subpopulations, including the transcription factor Sox9. Using in utero electroporation in embryonic mice of either sex, we demonstrate that elevated Sox9 expression in progenitors affects RGC cell cycle duration and leads to the generation of upper layer cortical neurons. Our data thus reveal molecular differences between progenitor cells with different neurogenic behavior at early stages of corticogenesis and indicates that Sox9 is critical for the maintenance of RGCs to regulate the generation of upper layer neurons.SIGNIFICANCE STATEMENT The existence of heterogeneity in the pool of RGCs and its relationship with the generation of cellular diversity in the cerebral cortex has been an interesting topic of debate for many years. Here we describe the existence of RGCs with reduced neurogenic behavior at early embryonic ages presenting a particular molecular signature. This molecular signature consists of differential expression of some genes including the transcription factor Sox9, which has been found to be a specific regulator of this subpopulation of progenitor cells. Functional experiments perturbing expression levels of Sox9 reveal its instructive role in the regulation of the neurogenic behavior of RGCs and its relationship with the generation of upper layer projection neurons at later ages.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Regulación del Desarrollo de la Expresión Génica / Neocórtex / Factor de Transcripción SOX9 / Neurogénesis / Células Ependimogliales / Autorrenovación de las Células / Proteínas del Tejido Nervioso Tipo de estudio: Prognostic_studies Límite: Animals / Pregnancy Idioma: En Año: 2021 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Regulación del Desarrollo de la Expresión Génica / Neocórtex / Factor de Transcripción SOX9 / Neurogénesis / Células Ependimogliales / Autorrenovación de las Células / Proteínas del Tejido Nervioso Tipo de estudio: Prognostic_studies Límite: Animals / Pregnancy Idioma: En Año: 2021 Tipo del documento: Article