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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.
Afiliación
  • Feng G; Department of Brain and Cognitive Sciences, McGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge, MA 02139; fengg@mit.edu frances.jensen@pennmedicine.upenn.edu bnewsome@stanford.edu jhmorrison@ucdavis.edu.
  • Jensen FE; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA 02142.
  • Greely HT; Department of Neurology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104; fengg@mit.edu frances.jensen@pennmedicine.upenn.edu bnewsome@stanford.edu jhmorrison@ucdavis.edu.
  • Okano H; Center for Law and the Biosciences, Stanford University, Stanford, CA 94305.
  • Treue S; Department of Physiology, Keio University School of Medicine, Shinjukuku, 160-8592 Tokyo, Japan.
  • Roberts AC; Laboratory for Marmoset Neural Architecture, RIKEN Center for Brain Science, 351-0106 Saitama, Wakoshi, Japan.
  • Fox JG; Cognitive Neuroscience Laboratory, German Primate Center-Leibniz Institute for Primate Research, 37077 Goettingen, Germany.
  • Caddick S; Faculty of Biology and Psychology, University of Goettingen, 37073 Goettingen, Germany.
  • Poo MM; Department of Physiology, Development, and Neuroscience, University of Cambridge, CB2 3DY Cambridge, United Kingdom.
  • Newsome WT; Division of Comparative Medicine, Massachusetts Institute of Technology, Cambridge, MA 02139.
  • Morrison JH; The Gatsby Charitable Foundation, SW1V 1AP London, United Kingdom.
Proc Natl Acad Sci U S A ; 117(39): 24022-24031, 2020 09 29.
Article en En | MEDLINE | ID: mdl-32817435
ABSTRACT
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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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Primates / Experimentación Animal / Modelos Animales de Enfermedad / Trastornos Mentales / Enfermedades del Sistema Nervioso Tipo de estudio: Diagnostic_studies / Guideline Límite: Animals Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Primates / Experimentación Animal / Modelos Animales de Enfermedad / Trastornos Mentales / Enfermedades del Sistema Nervioso Tipo de estudio: Diagnostic_studies / Guideline Límite: Animals Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2020 Tipo del documento: Article