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Egr1-EGFP transgenic mouse allows in vivo recording of Egr1 expression and neural activity | |
2021-11-01 | |
发表期刊 | JOURNAL OF NEUROSCIENCE METHODS (IF:2.7[JCR-2023],2.7[5-Year]) |
ISSN | 0165-0270 |
EISSN | 1872-678X |
卷号 | 363 |
DOI | 10.1016/j.jneumeth.2021.109350 |
摘要 | Background: Immediate-early genes (IEGs) have been serving as markers of active neurons for their rapid responses to stimulation. With the development of IEG-EGFP reporters by the GENSAT project, application of the IEGs have been greatly expanded. However, detailed validations for these systems are still lacking, causing trouble in the interpretation of the fluorescence signals. New method: In this work, taken Egr1-EGFP transgenic mice as an example, we proposed an improvement for the usage of the Egr1-EGFP reporter system based on detailed validation of its fluorescence signals. Results: Firstly, the exogenous EGFP mRNA levels were linearly correlated with the endogenous Egr1 mRNA levels in neurons. Secondly, the 3-hr-changes of the Egr1-EGFP signals before and after the stimulus were positively correlated with the stimulus-induced neuronal activities. Interestingly, persistent neuronal activity patterns in the post-stimulus phase also showed correlation with the stimulus-induced Egr1-EGFP signal changes. Furthermore, enriched environments engaged dramatic neuronal activations, allowing detailed characterization of Egr1EGFP expression dynamics Comparison with existing method(s): People used to infer the neuronal activities based on the raw fluorescence signals of IEG-EGFP reporter system, which was strongly obstructed by distinct protein regulation or dynamic properties between the EGFP and the IEGs. We demonstrated a better way for data analysis and experimental design. Conclusions: Taken together, this work proves that Egr1-EGFP signal is weakly but significantly correlated to task induced neural activity and gives detailed characterization of the signal dynamics. It not only provides basis for the understanding of the IEG-EGFP fluorescence signals but also offers instructions for proper experimental design with IEG-EGFP reporter systems. |
关键词 | Immediate-early gene Egr1-EGFP transgenic mouse in vivo imaging Activity-dependent Enriched environment |
收录类别 | SCIE |
语种 | 英语 |
WOS研究方向 | Biochemistry & Molecular Biology ; Neurosciences & Neurology |
WOS类目 | Biochemical Research Methods ; Neurosciences |
WOS记录号 | WOS:000704348900008 |
出版者 | ELSEVIER |
原始文献类型 | Article |
引用统计 | 正在获取...
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文献类型 | 期刊论文 |
条目标识符 | https://kms.shanghaitech.edu.cn/handle/2MSLDSTB/128413 |
专题 | 生命科学与技术学院_博士生 生命科学与技术学院_PI研究组_管吉松组 |
通讯作者 | Guan, Ji-Song |
作者单位 | 1.ShanghaiTech Univ, Sch Life Sci & Technol, Shanghai 201210, Peoples R China; 2.Inst Brain Intelligence Sci & Technol, Shanghai Res Ctr Brain Sci & Brain Inspired Intel, Shanghai 201210, Peoples R China; 3.Univ Shanghai Sci & Technol, Ctr Artificial Intelligence Nanophoton, Shanghai 200093, Peoples R China; 4.Tsinghua Univ, Sch Life Sci, IDG McGovern Inst Brain Res Tsinghua, MOE Key Lab Prot Sci, Beijing 100084, Peoples R China |
第一作者单位 | 生命科学与技术学院 |
通讯作者单位 | 生命科学与技术学院 |
第一作者的第一单位 | 生命科学与技术学院 |
推荐引用方式 GB/T 7714 | Wang, Guangyu,Xie, Hong,Hu, Yi,et al. Egr1-EGFP transgenic mouse allows in vivo recording of Egr1 expression and neural activity[J]. JOURNAL OF NEUROSCIENCE METHODS,2021,363. |
APA | Wang, Guangyu.,Xie, Hong.,Hu, Yi.,Chen, Qinan.,Liu, Chenhui.,...&Guan, Ji-Song.(2021).Egr1-EGFP transgenic mouse allows in vivo recording of Egr1 expression and neural activity.JOURNAL OF NEUROSCIENCE METHODS,363. |
MLA | Wang, Guangyu,et al."Egr1-EGFP transgenic mouse allows in vivo recording of Egr1 expression and neural activity".JOURNAL OF NEUROSCIENCE METHODS 363(2021). |
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