4.1 Article

Exclusive labeling of direct and indirect pathway neurons in the mouse neostriatum by an adeno- associated virus vector with Cre/lox system

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卷 2, 期 1, 页码 -

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ELSEVIER
DOI: 10.1016/j.xpro.2020.100230

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资金

  1. Ministry of Education, Culture, Sports, Science and Technology (MEXT)
  2. Japan Society for the Promotion of Science (JSPS) [JP18K14844]
  3. Scientific Research [JP20K07231, JP17K08522, JP20H03549, JP16H04663]
  4. Exploratory Research [JP20K20671, JP17K19451]
  5. Scientific Research on Innovative Areas, Adaptive Circuit Shift [JP26112001, JP15H01430]
  6. Hyper-Adaptability [JP20H05484]
  7. Resonance Bio [JP18H04743]
  8. Japan Agency for Medical Research and Development (AMED) [JP20dm0207063, JP20dm0207064]
  9. Research Institute for Diseases of Old Age at the Juntendo University School of Medicine [X1915, X1904]
  10. MEXT Private University Research Branding Project (Juntendo University)

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A novel AAV vector-based technique has been developed to label mouse neostriatal neurons with different fluorescent proteins and analyze their axonal projections. The technique shows high specificity and effectiveness in marking cell populations dependent on specific gene expression.
We developed an adeno-associated virus (AAV) vector-based technique to label mouse neostriatal neurons comprising direct and indirect pathways with different fluorescent proteins and analyze their axonal projections. The AAV vector expresses GFP or RFP in the presence or absence of Cre recombinase and should be useful for labeling two cell populations exclusively dependent on its expression. Here, we describe the AAV vector design, stereotaxic injection of the AAV vector, and a highly sensitive immunoperoxidase method for axon visualization.For complete details on the use and execution of this protocol, please refer to Okamoto et al. (2020).

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