| Literature DB >> 30888608 |
Fan Jia1,2,3, Xutao Zhu4,5, Pei Lv4, Liang Hu4, Qing Liu6,4, Sen Jin5, Fuqiang Xu7,8,9,10.
Abstract
Sparse labeling of neurons contributes to uncovering their morphology, and rapid expression of a fluorescent protein reduces the experiment range. To achieve the goal of rapid and sparse labeling of neurons in vivo, we established a rapid method for depicting the fine structure of neurons at 24 h post-infection based on a mutant virus-like particle of Semliki Forest virus. Approximately 0.014 fluorescent focus-forming units of the mutant virus-like particle transferred enhanced green fluorescent protein into neurons in vivo, and its affinity for neurons in vivo was stronger than for neurons in vitro and BHK21 (baby hamster kidney) cells. Collectively, the mutant virus-like particle provides a robust and convenient way to reveal the fine structure of neurons and is expected to be a helper virus for combining with other tools to determine their connectivity. Our work adds a new tool to the approaches for rapid and sparse labeling of neurons in vivo.Entities:
Keywords: Mutant virus-like particle; Neuronal morphology; Rapid labeling; Semliki Forest virus; Sparse labeling
Mesh:
Substances:
Year: 2019 PMID: 30888608 PMCID: PMC6527643 DOI: 10.1007/s12264-019-00362-z
Source DB: PubMed Journal: Neurosci Bull ISSN: 1995-8218 Impact factor: 5.203