Progress and Prospects for Genetic Modification of Nonhuman Primate Models in Biomedical Research

被引:73
作者
Chan, Anthony W. S. [1 ,2 ]
机构
[1] Emory Univ, Dept Human Genet, Sch Med, Atlanta, GA 30329 USA
[2] Yerkes Natl Primate Res Ctr, Div Neuropharmacol & Neurol Dis, Atlanta, GA USA
关键词
animal model; human diseases; nonhuman primates; transgenesis; PLURIPOTENT STEM-CELLS; EARLY HUNTINGTONS-DISEASE; FOREIGN DNA TRANSMISSION; ZINC-FINGER NUCLEASES; IN MOUSE MODEL; ANIMAL-MODELS; RHESUS-MONKEY; ES CELLS; HOMOLOGOUS RECOMBINATION; MILLISECOND-TIMESCALE;
D O I
10.1093/ilar/ilt035
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
The growing interest of modeling human diseases using genetically modified (transgenic) nonhuman primates (NHPs) is a direct result of NHPs (rhesus macaque, etc.) close relation to humans. NHPs share similar developmental paths with humans in their anatomy, physiology, genetics, and neural functions; and in their cognition, emotion, and social behavior. The NHP model within biomedical research has played an important role in the development of vaccines, assisted reproductive technologies, and new therapies for many diseases. Biomedical research has not been the primary role of NHPs. They have mainly been used for safety evaluation and pharmacokinetics studies, rather than determining therapeutic efficacy. The development of the first transgenic rhesus macaque (2001) revolutionized the role of NHP models in biomedicine. Development of the transgenic NHP model of Huntingtons disease (2008), with distinctive clinical features, further suggested the uniqueness of the model system; and the potential role of the NHP model for human genetic disorders. Modeling human genetic diseases using NHPs will continue to thrive because of the latest advances in molecular, genetic, and embryo technologies. NHPs rising role in biomedical research, specifically pre-clinical studies, is foreseeable. The path toward the development of transgenic NHPs and the prospect of transgenic NHPs in their new role in future biomedicine needs to be reviewed. This article will focus on the advancement of transgenic NHPs in the past decade, including transgenic technologies and disease modeling. It will outline new technologies that may have significant impact in future NHP modeling and will conclude with a discussion of the future prospects of the transgenic NHP model.
引用
收藏
页码:211 / 223
页数:13
相关论文
共 202 条
[1]  
Abdel-Salam OME, 2011, CNS NEUROL DISORD-DR, V10, P459
[2]   MicroRNA pathways in flies and worms: Growth, death, fat, stress, and timing [J].
Ambros, V .
CELL, 2003, 113 (06) :673-676
[3]   The evolution of our thinking about microRNAs [J].
Ambros, Victor .
NATURE MEDICINE, 2008, 14 (10) :1036-1040
[4]   Genetic Correction of Huntington's Disease Phenotypes in Induced Pluripotent Stem Cells [J].
An, Mahru C. ;
Zhang, Ningzhe ;
Scott, Gary ;
Montoro, Daniel ;
Wittkop, Tobias ;
Mooney, Sean ;
Melov, Simon ;
Ellerby, Lisa M. .
CELL STEM CELL, 2012, 11 (02) :253-263
[5]   Complex movement behaviour and progression of Huntington's disease [J].
Andrich, Juergen ;
Saft, Carsten ;
Ostholt, Natalie ;
Mueller, Thomas .
NEUROSCIENCE LETTERS, 2007, 416 (03) :272-274
[6]  
[Anonymous], 1994, Manipulating the mouse embryo: a laboratory manual
[7]   Effects of selective neonatal temporal lobe lesions on socioemotional behavior in infant rhesus monkeys (Macaca mulatta) [J].
Bachevalier, J ;
Málková, L ;
Mishkin, M .
BEHAVIORAL NEUROSCIENCE, 2001, 115 (03) :545-559
[8]   Memory for spatial location and object-place associations are differently processed by the hippocampal formation, parahippocampal areas TH/TF and perirhinal cortex [J].
Bachevalier, Jocelyne ;
Nemanic, Sarah .
HIPPOCAMPUS, 2008, 18 (01) :64-80
[9]   Behavioral outcomes of late-onset or early-onset orbital frontal cortex (areas 11/13) lesions in rhesus monkeys [J].
Bachevalier, Jocelyne ;
Machado, Christopher J. ;
Kazama, Andy .
CRITICAL CONTRIBUTIONS OF THE ORBITOFRONTAL CORTEX TO BEHAVIOR, 2011, 1239 :71-86
[10]   Clinical and Biomarker Changes in Dominantly Inherited Alzheimer's Disease [J].
Bateman, Randall J. ;
Xiong, Chengjie ;
Benzinger, Tammie L. S. ;
Fagan, Anne M. ;
Goate, Alison ;
Fox, Nick C. ;
Marcus, Daniel S. ;
Cairns, Nigel J. ;
Xie, Xianyun ;
Blazey, Tyler M. ;
Holtzman, David M. ;
Santacruz, Anna ;
Buckles, Virginia ;
Oliver, Angela ;
Moulder, Krista ;
Aisen, Paul S. ;
Ghetti, Bernardino ;
Klunk, William E. ;
McDade, Eric ;
Martins, Ralph N. ;
Masters, Colin L. ;
Mayeux, Richard ;
Ringman, John M. ;
Rossor, Martin N. ;
Schofield, Peter R. ;
Sperling, Reisa A. ;
Salloway, Stephen ;
Morris, John C. .
NEW ENGLAND JOURNAL OF MEDICINE, 2012, 367 (09) :795-804