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Human Cerebral Organoids and Fetal Brain Tissue Share Proteomic Similarities

The limited access to functional human brain tissue has led to the development of stem cell-based alternative models. The differentiation of human pluripotent stem cells into cerebral organoids with self-organized architecture has created novel opportunities to study the early stages of the human ce...

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Detalles Bibliográficos
Autores principales: Nascimento, Juliana Minardi, Saia-Cereda, Verônica M., Sartore, Rafaela C., da Costa, Rodrigo Madeiro, Schitine, Clarissa S., Freitas, Hercules Rezende, Murgu, Michael, de Melo Reis, Ricardo A., Rehen, Stevens K., Martins-de-Souza, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6893972/
https://www.ncbi.nlm.nih.gov/pubmed/31850342
http://dx.doi.org/10.3389/fcell.2019.00303
Descripción
Sumario:The limited access to functional human brain tissue has led to the development of stem cell-based alternative models. The differentiation of human pluripotent stem cells into cerebral organoids with self-organized architecture has created novel opportunities to study the early stages of the human cerebral formation. Here we applied state-of-the-art label-free shotgun proteomics to compare the proteome of stem cell-derived cerebral organoids to the human fetal brain. We identified 3,073 proteins associated with different developmental stages, from neural progenitors to neurons, astrocytes, or oligodendrocytes. The major protein groups are associated with neurogenesis, axon guidance, synaptogenesis, and cortical brain development. Glial cell proteins related to cell growth and maintenance, energy metabolism, cell communication, and signaling were also described. Our data support the variety of cells and neural network functional pathways observed within cell-derived cerebral organoids, confirming their usefulness as an alternative model. The characterization of brain organoid proteome is key to explore, in a dish, atypical and disrupted processes during brain development or neurodevelopmental, neurodegenerative, and neuropsychiatric diseases.