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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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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 |
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author | 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 |
author_facet | 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 |
author_sort | Nascimento, Juliana Minardi |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6893972 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68939722019-12-17 Human Cerebral Organoids and Fetal Brain Tissue Share Proteomic Similarities 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 Front Cell Dev Biol Cell and Developmental Biology 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. Frontiers Media S.A. 2019-11-28 /pmc/articles/PMC6893972/ /pubmed/31850342 http://dx.doi.org/10.3389/fcell.2019.00303 Text en Copyright © 2019 Nascimento, Saia-Cereda, Sartore, Madeiro da Costa, Schitine, Freitas, Murgu, de Melo Reis, Rehen and Martins-de-Souza. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology 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 Human Cerebral Organoids and Fetal Brain Tissue Share Proteomic Similarities |
title | Human Cerebral Organoids and Fetal Brain Tissue Share Proteomic Similarities |
title_full | Human Cerebral Organoids and Fetal Brain Tissue Share Proteomic Similarities |
title_fullStr | Human Cerebral Organoids and Fetal Brain Tissue Share Proteomic Similarities |
title_full_unstemmed | Human Cerebral Organoids and Fetal Brain Tissue Share Proteomic Similarities |
title_short | Human Cerebral Organoids and Fetal Brain Tissue Share Proteomic Similarities |
title_sort | human cerebral organoids and fetal brain tissue share proteomic similarities |
topic | Cell and Developmental Biology |
url | 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 |
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