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Stem cell models of human synapse development and degeneration

Many brain disorders exhibit altered synapse formation in development or synapse loss with age. To understand the complexities of human synapse development and degeneration, scientists now engineer neurons and brain organoids from human-induced pluripotent stem cells (hIPSC). These hIPSC-derived bra...

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Detalles Bibliográficos
Autores principales: Wilson, Emily S., Newell-Litwa, Karen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6329912/
https://www.ncbi.nlm.nih.gov/pubmed/30475098
http://dx.doi.org/10.1091/mbc.E18-04-0222
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author Wilson, Emily S.
Newell-Litwa, Karen
author_facet Wilson, Emily S.
Newell-Litwa, Karen
author_sort Wilson, Emily S.
collection PubMed
description Many brain disorders exhibit altered synapse formation in development or synapse loss with age. To understand the complexities of human synapse development and degeneration, scientists now engineer neurons and brain organoids from human-induced pluripotent stem cells (hIPSC). These hIPSC-derived brain models develop both excitatory and inhibitory synapses and functional synaptic activity. In this review, we address the ability of hIPSC-derived brain models to recapitulate synapse development and insights gained into the molecular mechanisms underlying synaptic alterations in neuronal disorders. We also discuss the potential for more accurate human brain models to advance our understanding of synapse development, degeneration, and therapeutic responses.
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spelling pubmed-63299122019-02-10 Stem cell models of human synapse development and degeneration Wilson, Emily S. Newell-Litwa, Karen Mol Biol Cell Perspective Many brain disorders exhibit altered synapse formation in development or synapse loss with age. To understand the complexities of human synapse development and degeneration, scientists now engineer neurons and brain organoids from human-induced pluripotent stem cells (hIPSC). These hIPSC-derived brain models develop both excitatory and inhibitory synapses and functional synaptic activity. In this review, we address the ability of hIPSC-derived brain models to recapitulate synapse development and insights gained into the molecular mechanisms underlying synaptic alterations in neuronal disorders. We also discuss the potential for more accurate human brain models to advance our understanding of synapse development, degeneration, and therapeutic responses. The American Society for Cell Biology 2018-11-26 /pmc/articles/PMC6329912/ /pubmed/30475098 http://dx.doi.org/10.1091/mbc.E18-04-0222 Text en © 2018 Wilson and Newell-Litwa. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. http://creativecommons.org/licenses/by-nc-sa/3.0 This article is distributed by The American Socity for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License.
spellingShingle Perspective
Wilson, Emily S.
Newell-Litwa, Karen
Stem cell models of human synapse development and degeneration
title Stem cell models of human synapse development and degeneration
title_full Stem cell models of human synapse development and degeneration
title_fullStr Stem cell models of human synapse development and degeneration
title_full_unstemmed Stem cell models of human synapse development and degeneration
title_short Stem cell models of human synapse development and degeneration
title_sort stem cell models of human synapse development and degeneration
topic Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6329912/
https://www.ncbi.nlm.nih.gov/pubmed/30475098
http://dx.doi.org/10.1091/mbc.E18-04-0222
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