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摘要:
The proper formation of synapses is essential for brain function. Synaptic cell adhesion molecules (CAMs) are thought to play essential roles in the initiation of the synapse formation process. The artificial synapse formation assay, in which non-neuronal cells and neurons are co-cultured, has been shown to be a powerful system for screening CAMs. However;controlling a large number of cell pools in co-culture is complicated, creating a potential barrier for high-throughput screening. This protocol describes a new co-culture method in which cDNA plasmid is transfected into human embryonic kidney 293T cells using polyetherimide 24 h after cells were mixed with neurons, and immunostaining and confocal imaging are employed for analyzing synaptogenesis. This optimized method is simpler and easier to perform than the traditional method for the examination of the synaptogenic activities of individual cell-surface proteins in isolation, and provides an unbiased screening platform for synaptogenic proteins.
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篇名 A new co-culture method for identifying synaptic adhesion molecules involved in synapse formation
来源期刊 生物物理学报:英文版 学科 生物学
关键词 CO-CULTURE ASSAY SYNAPSE formation SYNAPTIC cell adhesion MOLECULES POLYETHERIMIDE
年,卷(期) 2019,(2) 所属期刊栏目
研究方向 页码范围 91-97
页数 7页 分类号 Q
字数 语种
DOI
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研究主题发展历程
节点文献
CO-CULTURE
ASSAY
SYNAPSE
formation
SYNAPTIC
cell
adhesion
MOLECULES
POLYETHERIMIDE
研究起点
研究来源
研究分支
研究去脉
引文网络交叉学科
相关学者/机构
期刊影响力
生物物理学报:英文版
双月刊
2364-3439
10-1302/Q
Institute of Biophys
出版文献量(篇)
32
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0
总被引数(次)
0
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