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Human Cortical Organoids Expose a Differential Function of GSK3 on Cortical Neurogenesis

The regulation of the proliferation and polarity of neural progenitors is crucial for the development of the brain cortex. Animal studies have implicated glycogen synthase kinase 3 (GSK3) as a pivotal regulator of both proliferation and polarity, yet the functional relevance of its signaling for the...

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Detalles Bibliográficos
Autores principales: López-Tobón, Alejandro, Villa, Carlo Emanuele, Cheroni, Cristina, Trattaro, Sebastiano, Caporale, Nicolò, Conforti, Paola, Iennaco, Raffaele, Lachgar, Maria, Rigoli, Marco Tullio, Marcó de la Cruz, Berta, Lo Riso, Pietro, Tenderini, Erika, Troglio, Flavia, De Simone, Marco, Liste-Noya, Isabel, Macino, Giuseppe, Pagani, Massimiliano, Cattaneo, Elena, Testa, Giuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6893153/
https://www.ncbi.nlm.nih.gov/pubmed/31607568
http://dx.doi.org/10.1016/j.stemcr.2019.09.005
Descripción
Sumario:The regulation of the proliferation and polarity of neural progenitors is crucial for the development of the brain cortex. Animal studies have implicated glycogen synthase kinase 3 (GSK3) as a pivotal regulator of both proliferation and polarity, yet the functional relevance of its signaling for the unique features of human corticogenesis remains to be elucidated. We harnessed human cortical brain organoids to probe the longitudinal impact of GSK3 inhibition through multiple developmental stages. Chronic GSK3 inhibition increased the proliferation of neural progenitors and caused massive derangement of cortical tissue architecture. Single-cell transcriptome profiling revealed a direct impact on early neurogenesis and uncovered a selective role of GSK3 in the regulation of glutamatergic lineages and outer radial glia output. Our dissection of the GSK3-dependent transcriptional network in human corticogenesis underscores the robustness of the programs determining neuronal identity independent of tissue architecture.