Opportunities and limitations of genetically modified nonhuman primate models for neuroscience research

© 2020 National Academy of Sciences. All rights reserved. The recently developed new genome-editing technologies, such as the CRISPR/Cas system, have opened the door for generating genetically modified nonhuman primate (NHP) models for basic neuroscience and brain disorders research. The complex cir...

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Main Authors: Feng, Guoping, Jensen, Frances E, Greely, Henry T, Okano, Hideyuki, Treue, Stefan, Roberts, Angela C, Fox, James G, Caddick, Sarah, Poo, Mu-ming, Newsome, William T, Morrison, John H
Other Authors: Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences
Format: Article
Language:English
Published: Proceedings of the National Academy of Sciences 2021
Online Access:https://hdl.handle.net/1721.1/135479
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author Feng, Guoping
Jensen, Frances E
Greely, Henry T
Okano, Hideyuki
Treue, Stefan
Roberts, Angela C
Fox, James G
Caddick, Sarah
Poo, Mu-ming
Newsome, William T
Morrison, John H
author2 Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences
author_facet Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences
Feng, Guoping
Jensen, Frances E
Greely, Henry T
Okano, Hideyuki
Treue, Stefan
Roberts, Angela C
Fox, James G
Caddick, Sarah
Poo, Mu-ming
Newsome, William T
Morrison, John H
author_sort Feng, Guoping
collection MIT
description © 2020 National Academy of Sciences. All rights reserved. The recently developed new genome-editing technologies, such as the CRISPR/Cas system, have opened the door for generating genetically modified nonhuman primate (NHP) models for basic neuroscience and brain disorders research. The complex circuit formation and experience-dependent refinement of the human brain are very difficult to model in vitro, and thus require use of in vivo whole-animal models. For many neurodevelopmental and psychiatric disorders, abnormal circuit formation and refinement might be at the center of their pathophysiology. Importantly, many of the critical circuits and regional cell populations implicated in higher human cognitive function and in many psychiatric disorders are not present in lower mammalian brains, while these analogous areas are replicated in NHP brains. Indeed, neuropsychiatric disorders represent a tremendous health and economic burden globally. The emerging field of genetically modified NHP models has the potential to transform our study of higher brain function and dramatically facilitate the development of effective treatment for human brain disorders. In this paper, we discuss the importance of developing such models, the infrastructure and training needed to maximize the impact of such models, and ethical standards required for using these models.
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spelling mit-1721.1/1354792023-09-15T18:58:38Z Opportunities and limitations of genetically modified nonhuman primate models for neuroscience research Feng, Guoping Jensen, Frances E Greely, Henry T Okano, Hideyuki Treue, Stefan Roberts, Angela C Fox, James G Caddick, Sarah Poo, Mu-ming Newsome, William T Morrison, John H Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences McGovern Institute for Brain Research at MIT Massachusetts Institute of Technology. Division of Comparative Medicine © 2020 National Academy of Sciences. All rights reserved. The recently developed new genome-editing technologies, such as the CRISPR/Cas system, have opened the door for generating genetically modified nonhuman primate (NHP) models for basic neuroscience and brain disorders research. The complex circuit formation and experience-dependent refinement of the human brain are very difficult to model in vitro, and thus require use of in vivo whole-animal models. For many neurodevelopmental and psychiatric disorders, abnormal circuit formation and refinement might be at the center of their pathophysiology. Importantly, many of the critical circuits and regional cell populations implicated in higher human cognitive function and in many psychiatric disorders are not present in lower mammalian brains, while these analogous areas are replicated in NHP brains. Indeed, neuropsychiatric disorders represent a tremendous health and economic burden globally. The emerging field of genetically modified NHP models has the potential to transform our study of higher brain function and dramatically facilitate the development of effective treatment for human brain disorders. In this paper, we discuss the importance of developing such models, the infrastructure and training needed to maximize the impact of such models, and ethical standards required for using these models. 2021-10-27T20:23:37Z 2021-10-27T20:23:37Z 2020 2021-03-19T15:55:34Z Article http://purl.org/eprint/type/JournalArticle https://hdl.handle.net/1721.1/135479 en 10.1073/PNAS.2006515117 Proceedings of the National Academy of Sciences of the United States of America Creative Commons Attribution-NonCommercial-NoDerivs License http://creativecommons.org/licenses/by-nc-nd/4.0/ application/pdf Proceedings of the National Academy of Sciences PNAS
spellingShingle Feng, Guoping
Jensen, Frances E
Greely, Henry T
Okano, Hideyuki
Treue, Stefan
Roberts, Angela C
Fox, James G
Caddick, Sarah
Poo, Mu-ming
Newsome, William T
Morrison, John H
Opportunities and limitations of genetically modified nonhuman primate models for neuroscience research
title Opportunities and limitations of genetically modified nonhuman primate models for neuroscience research
title_full Opportunities and limitations of genetically modified nonhuman primate models for neuroscience research
title_fullStr Opportunities and limitations of genetically modified nonhuman primate models for neuroscience research
title_full_unstemmed Opportunities and limitations of genetically modified nonhuman primate models for neuroscience research
title_short Opportunities and limitations of genetically modified nonhuman primate models for neuroscience research
title_sort opportunities and limitations of genetically modified nonhuman primate models for neuroscience research
url https://hdl.handle.net/1721.1/135479
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