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Comparative study of the transfection efficiency of commonly used viral vectors in rhesus monkey (Macaca mulatta) brains

Viral vector transfection systems are among the simplest of biological agents with the ability to transfer genes into the central nervous system. In brain research, a series of powerful and novel gene editing technologies are based on these systems. Although many viral vectors are used in rodents, t...

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Autores principales: Wu, Shi-Hao, Liao, Zhi-Xing, Rizak, Joshua D., Zheng, Na, Zhang, Lin-Heng, Tang, Hen, He, Xiao-Bin, Wu, Yang, He, Xia-Ping, Yang, Mei-Feng, Li, Zheng-Hui, Qin, Dong-Dong, Hu, Xin-Tian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Science Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5396031/
https://www.ncbi.nlm.nih.gov/pubmed/28409504
http://dx.doi.org/10.24272/j.issn.2095-8137.2017.015
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author Wu, Shi-Hao
Liao, Zhi-Xing
Rizak, Joshua D.
Zheng, Na
Zhang, Lin-Heng
Tang, Hen
He, Xiao-Bin
Wu, Yang
He, Xia-Ping
Yang, Mei-Feng
Li, Zheng-Hui
Qin, Dong-Dong
Hu, Xin-Tian
author_facet Wu, Shi-Hao
Liao, Zhi-Xing
Rizak, Joshua D.
Zheng, Na
Zhang, Lin-Heng
Tang, Hen
He, Xiao-Bin
Wu, Yang
He, Xia-Ping
Yang, Mei-Feng
Li, Zheng-Hui
Qin, Dong-Dong
Hu, Xin-Tian
author_sort Wu, Shi-Hao
collection PubMed
description Viral vector transfection systems are among the simplest of biological agents with the ability to transfer genes into the central nervous system. In brain research, a series of powerful and novel gene editing technologies are based on these systems. Although many viral vectors are used in rodents, their full application has been limited in non-human primates. To identify viral vectors that can stably and effectively express exogenous genes within non-human primates, eleven commonly used recombinant adeno-associated viral and lentiviral vectors, each carrying a gene to express green or red fluorescence, were injected into the parietal cortex of four rhesus monkeys. The expression of fluorescent cells was used to quantify transfection efficiency. Histological results revealed that recombinant adeno-associated viral vectors, especially the serotype 2/9 coupled with the cytomegalovirus, human synapsin Ⅰ, or Ca(2+)/calmodulin-dependent protein kinase Ⅱ promoters, and lentiviral vector coupled with the human ubiquitin C promoter, induced higher expression of fluorescent cells, representing high transfection efficiency. This is the first comparison of transfection efficiencies of different viral vectors carrying different promoters and serotypes in non-human primates (NHPs). These results can be used as an aid to select optimal vectors to transfer exogenous genes into the central nervous system of non-human primates.
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spelling pubmed-53960312017-04-24 Comparative study of the transfection efficiency of commonly used viral vectors in rhesus monkey (Macaca mulatta) brains Wu, Shi-Hao Liao, Zhi-Xing Rizak, Joshua D. Zheng, Na Zhang, Lin-Heng Tang, Hen He, Xiao-Bin Wu, Yang He, Xia-Ping Yang, Mei-Feng Li, Zheng-Hui Qin, Dong-Dong Hu, Xin-Tian Zool Res Reports Viral vector transfection systems are among the simplest of biological agents with the ability to transfer genes into the central nervous system. In brain research, a series of powerful and novel gene editing technologies are based on these systems. Although many viral vectors are used in rodents, their full application has been limited in non-human primates. To identify viral vectors that can stably and effectively express exogenous genes within non-human primates, eleven commonly used recombinant adeno-associated viral and lentiviral vectors, each carrying a gene to express green or red fluorescence, were injected into the parietal cortex of four rhesus monkeys. The expression of fluorescent cells was used to quantify transfection efficiency. Histological results revealed that recombinant adeno-associated viral vectors, especially the serotype 2/9 coupled with the cytomegalovirus, human synapsin Ⅰ, or Ca(2+)/calmodulin-dependent protein kinase Ⅱ promoters, and lentiviral vector coupled with the human ubiquitin C promoter, induced higher expression of fluorescent cells, representing high transfection efficiency. This is the first comparison of transfection efficiencies of different viral vectors carrying different promoters and serotypes in non-human primates (NHPs). These results can be used as an aid to select optimal vectors to transfer exogenous genes into the central nervous system of non-human primates. Science Press 2017-03-18 /pmc/articles/PMC5396031/ /pubmed/28409504 http://dx.doi.org/10.24272/j.issn.2095-8137.2017.015 Text en http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Reports
Wu, Shi-Hao
Liao, Zhi-Xing
Rizak, Joshua D.
Zheng, Na
Zhang, Lin-Heng
Tang, Hen
He, Xiao-Bin
Wu, Yang
He, Xia-Ping
Yang, Mei-Feng
Li, Zheng-Hui
Qin, Dong-Dong
Hu, Xin-Tian
Comparative study of the transfection efficiency of commonly used viral vectors in rhesus monkey (Macaca mulatta) brains
title Comparative study of the transfection efficiency of commonly used viral vectors in rhesus monkey (Macaca mulatta) brains
title_full Comparative study of the transfection efficiency of commonly used viral vectors in rhesus monkey (Macaca mulatta) brains
title_fullStr Comparative study of the transfection efficiency of commonly used viral vectors in rhesus monkey (Macaca mulatta) brains
title_full_unstemmed Comparative study of the transfection efficiency of commonly used viral vectors in rhesus monkey (Macaca mulatta) brains
title_short Comparative study of the transfection efficiency of commonly used viral vectors in rhesus monkey (Macaca mulatta) brains
title_sort comparative study of the transfection efficiency of commonly used viral vectors in rhesus monkey (macaca mulatta) brains
topic Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5396031/
https://www.ncbi.nlm.nih.gov/pubmed/28409504
http://dx.doi.org/10.24272/j.issn.2095-8137.2017.015
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