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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The American Society for Cell Biology
2018
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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. |
format | Online Article Text |
id | pubmed-6329912 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT wilsonemilys stemcellmodelsofhumansynapsedevelopmentanddegeneration AT newelllitwakaren stemcellmodelsofhumansynapsedevelopmentanddegeneration |