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

STAR Protoc. 2021 Nov 18;2(4):100964. doi: 10.1016/j.xpro.2021.100964. eCollection 2021 Dec 17.

Abstract

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).

Keywords: Cell Biology; Cell culture; Developmental biology; Microscopy; Neuroscience; Single Cell; Stem Cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • Cerebellum / cytology*
  • Cytological Techniques / methods*
  • Female
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Neural Stem Cells / cytology*