Daily two-photon neuronal population imaging with targeted single-cell electrophysiology and subcellular imaging in auditory cortex of behaving mice

被引:1
|
作者
Huang, Junjie [1 ]
Liang, Susu [1 ]
Li, Longhui [1 ]
Li, Xingyi [1 ]
Liao, Xiang [1 ]
Hu, Qianshuo [2 ]
Zhang, Chunqing [3 ,4 ]
Jia, Hongbo [5 ,6 ,7 ,8 ,9 ]
Chen, Xiaowei [3 ,4 ,10 ]
Wang, Meng [1 ]
Li, Ruijie [3 ,4 ,5 ]
机构
[1] Chongqing Univ, Ctr Neurointelligence, Sch Med, Chongqing, Peoples R China
[2] Chongqing Univ Technol, Sch Artificial Intelligence, Chongqing, Peoples R China
[3] Third Mil Med Univ, Brain Res Ctr, Chongqing, Peoples R China
[4] Third Mil Med Univ, State Key Lab Trauma Burns & Combined Injury, Chongqing, Peoples R China
[5] Guangxi Univ, Adv Inst Brain & Intelligence, Sch Phys Sci & Technol, Nanning, Peoples R China
[6] Chinese Acad Sci, Suzhou Inst Biomed Engn & Technol, Brain Res Instrument Innovat Ctr, Suzhou, Peoples R China
[7] Leibniz Inst Neurobiol, Magdeburg, Germany
[8] Tech Univ Munich, Inst Neurosci, Munich, Germany
[9] Tech Univ Munich, SyNergy Cluster, Munich, Germany
[10] Chongqing Inst Brain & Intelligence, Guangyang Bay Lab, Chongqing, Peoples R China
基金
中国国家自然科学基金;
关键词
daily two-photon Ca2+ imaging; auditory cortex; behaving mouse; dendritic spines; loose-patch recording; AWAKE; ELECTROPORATION; RESOLUTION;
D O I
10.3389/fncel.2023.1142267
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Quantitative and mechanistic understanding of learning and long-term memory at the level of single neurons in living brains require highly demanding techniques. A specific need is to precisely label one cell whose firing output property is pinpointed amidst a functionally characterized large population of neurons through the learning process and then investigate the distribution and properties of dendritic inputs. Here, we disseminate an integrated method of daily two-photon neuronal population Ca2+ imaging through an auditory associative learning course, followed by targeted single-cell loose-patch recording and electroporation of plasmid for enhanced chronic Ca2+ imaging of dendritic spines in the targeted cell. Our method provides a unique solution to the demand, opening a solid path toward the hard-cores of how learning and long-term memory are physiologically carried out at the level of single neurons and synapses.
引用
收藏
页数:12
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