Combining low-density cell culture, single-cell tracking, and patch-clamp to monitor the behavior of postnatal murine cerebellar neural stem cells

Low-density cell culture of the postnatal cerebellum, combined with live imaging and single-cell tracking, allows the behavior of postnatal cerebellar neural stem cells (NSCs) and their progeny to be monitored. Cultured cerebellar NSCs maintain their neurogenic nature giving rise, in the same relati...

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Bibliographic Details
Published inSTAR protocols Vol. 2; no. 4; p. 100964
Main Authors Menéndez-Méndez, Aida, Paniagua-Herranz, Lucía, Olivos-Oré, Luis A., Gómez-Villafuertes, Rosa, Pérez-Sen, Raquel, Delicado, Esmerilda G., Artalejo, Antonio R., Ortega, Felipe
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 17.12.2021
Elsevier
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Summary:Low-density cell culture of the postnatal cerebellum, combined with live imaging and single-cell tracking, allows the behavior of postnatal cerebellar neural stem cells (NSCs) and their progeny to be monitored. Cultured cerebellar NSCs maintain their neurogenic nature giving rise, in the same relative proportions that exist in vivo, to the neuronal progeny generated by the three postnatal cerebellar neurogenic niches. This protocol describes the identification of the nature of the progeny through both post-imaging immunocytochemistry and patch-clamp recordings. For complete details on the use and execution of this protocol, please refer to Paniagua-Herranz et al. (2020b). [Display omitted] •Protocol to culture postnatal mouse cerebellar neural stem cells (NSCs) in low density•The behavior of isolated postnatal cerebellar NSC can be monitored at single-cell level•Protocol for simultaneous monitoring of the three postnatal cerebellar neurogenic niches•Procedures of live imaging and single cell tracking for lineage tracing Low-density cell culture of the postnatal cerebellum, combined with live imaging and single-cell tracking, allows the behavior of postnatal cerebellar neural stem cells (NSCs) and their progeny to be monitored. Cultured cerebellar NSCs maintain their neurogenic nature giving rise, in the same relative proportions that exist in vivo, to the neuronal progeny generated by the three postnatal cerebellar neurogenic niches. This protocol describes the identification of the nature of the progeny through both post-imaging immunocytochemistry and patch-clamp recordings.
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Present address: Department of Physiology and Medical Physics, RCSI University of Medicine and Health Sciences, Dublin D02 YN77, Ireland
These authors contributed equally
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ISSN:2666-1667
2666-1667
DOI:10.1016/j.xpro.2021.100964