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Isolate and Culture Mouse Primary Neurons for West Nile Virus Infection

Part of the Methods in Molecular Biology book series (MIMB,volume 2585)

Abstract

Primary neurons are very valuable cells to study the pathogenesis of neurotropic viruses, such as West Nile virus. The mouse primary neurons can be used to assess viral infection profiles and cellular immune responses to a viral infection. However, successful isolation and culture of mouse neurons can be challenging. Here, we report a step-by-step method to prepare a primary neuron culture from adult mice.

Key words

  • Mouse primary neuron
  • Culture protocol
  • Neurotrophic virus
  • West Nile virus

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References

  1. Facci L, Skaper SD Culture of rodent cortical and hippocampal neurons. (1940–6029 (Electronic))

    Google Scholar 

  2. Sciarretta C, Minichiello L The preparation of primary cortical neuron cultures and a practical application using immunofluorescent cytochemistry. (1940–6029 (Electronic))

    Google Scholar 

  3. Ge H, Tan L, Wu P et al (2015) Poly-L-ornithine promotes preferred differentiation of neural stem/progenitor cells via ERK signalling pathway. Sci Rep 5:15535–15535. https://doi.org/10.1038/srep15535

    CrossRef  CAS  PubMed  PubMed Central  Google Scholar 

  4. Brunetti P, Basta G Faloerni A, Calcinaro F et al Immunoprotection of pancreatic islet grafts within artificial microcapsules. (0391–3988 (Print))

    Google Scholar 

  5. Herculano-Houzel S, Mota B, Lent R (2006) Cellular scaling rules for rodent brains. Proc Natl Acad Sci 103(32):12138. https://doi.org/10.1073/pnas.0604911103

    CrossRef  CAS  PubMed  PubMed Central  Google Scholar 

  6. Calvo-Garrido J, Winn D, Maffezzini C et al (2021) Protocol for the derivation, culturing, and differentiation of human iPS-cell-derived neuroepithelial stem cells to study neural differentiation in vitro. STAR Protoc 2(2):100528–100528. https://doi.org/10.1016/j.xpro.2021.100528

    CrossRef  CAS  PubMed  PubMed Central  Google Scholar 

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Acknowledgments

This work was supported in part by the National Institute of Allergy and Infectious Diseases of the National Institutes of Health R15AI135893 (F.B.).

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Correspondence to Fengwei Bai .

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© 2023 The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature

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Nazneen, F., Bai, F. (2023). Isolate and Culture Mouse Primary Neurons for West Nile Virus Infection. In: Bai, F. (eds) West Nile Virus. Methods in Molecular Biology, vol 2585. Humana, New York, NY. https://doi.org/10.1007/978-1-0716-2760-0_4

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  • DOI: https://doi.org/10.1007/978-1-0716-2760-0_4

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  • Publisher Name: Humana, New York, NY

  • Print ISBN: 978-1-0716-2759-4

  • Online ISBN: 978-1-0716-2760-0

  • eBook Packages: Springer Protocols