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Comparative study of the transfection efficiency of commonly used viral vectors in rhesus monkey (Macaca mulatta) brains 被引量:7
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作者 Shi-Hao Wu Zhi-Xing Liao +10 位作者 Joshua D. Rizak Na Zheng lin-heng zhang Hen Tang Xiao-Bin He Yang Wu Xia-Ping He Mei-Feng Yang Zheng-Hui Li Dong-Dong Qin Xin-Tian Hu 《Zoological Research》 CAS CSCD 2017年第2期88-95,共8页
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 technologi... 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 nonhuman 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 Ca2+/calmodulin-dependentproteinkinaseII 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. 展开更多
关键词 Recombinant adeno-associated virus LENTIVIRUS Rhesus monkey Central nervous system
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利用CRISPR/Cas9技术在活体青年猕猴脑内进行基因编辑诱导其出现孤独症谱系障碍的行为表型 被引量:4
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作者 吴诗昊 李霄 +13 位作者 秦冬冬 张琳恒 程田林 陈枝芳 聂彬彬 任晓峰 吴晶 王文超 胡英周 谷依琳 吕龙宝 尹勇 胡新天 仇子龙 《Science Bulletin》 SCIE EI CSCD 2021年第9期937-946,M0004,共11页
尽管CRISPR/Cas9基因编辑技术被广泛应用于人类疾病建模工作,但此前并无人利用该技术在非人灵长类脑内通过对疾病相关基因的编辑诱导出猕猴的行为表型.本研究利用AAV介导的CRISPR/Cas9技术,对活体猕猴海马脑区中与孤独症谱系障碍(ASD)... 尽管CRISPR/Cas9基因编辑技术被广泛应用于人类疾病建模工作,但此前并无人利用该技术在非人灵长类脑内通过对疾病相关基因的编辑诱导出猕猴的行为表型.本研究利用AAV介导的CRISPR/Cas9技术,对活体猕猴海马脑区中与孤独症谱系障碍(ASD)和瑞特综合症(RTT)发病密切相关的MECP2基因进行编辑,基因编辑组猕猴(n=7)与其自身基因编辑前作为对照,同时与注射空载病毒的对照组猕猴(n=4)相比,其在基因编辑后出现了部分与孤独症临床症状十分相似的行为学改变,包括社交障碍、睡眠节律紊乱、对外界刺激的迟钝和手部精细运动受损等.可是另一些典型的孤独症症状,比如刻板运动,又没有在这些基因编辑猴中被观察到.以上现象提示不同的脑区在该疾病中可能扮演不同的角色.本研究利用上述技术能够快速高效地在猕猴上复制出相关疾病的症状,也为今后探索快速成模的转基因工程猕猴疾病模型奠定了基础.此类猕猴模型将为脑疾病的机理研究以及治疗作出重要贡献. 展开更多
关键词 Autism spectrum disorders Nonhuman primate model Disease model Gene-editing
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