发布: 2020年07月05日第10卷第13期 DOI: 10.21769/BioProtoc.3674 浏览次数: 4859
评审: Geoffrey C. Y. LauWoojong LeeLinlin Sun
Abstract
Organotypic slice culture is a powerful technique for exploring the embryonic development of the mammalian brain. In this protocol we describe a basic slice culture technique we have used for two sets of experiments: axon guidance transplant assays and bead culture assays.
Keywords: Organotypic (器官型)Background
Organotypic slice culture is a technique that has been widely used in recent years and has been a particularly popular technique in the field of neurodevelopment. It has the great advantage of allowing the culture of developing neural cells in-vitro while maintaining the in-vivo structure of the tissue. In this protocol we describe the slice culture technique we used for two experiments from our recent paper (Clegg et al., 2019). Firstly we performed an axon guidance transplant assay whereby fluorescently labeled tissue was transplanted into a non-fluorescent host slice in order to observe axon outgrowth. This is a modified version of a protocol previously used to study the development of the corpus callosum, but could be easily adapted to examine other axon tracts such as the thalamocortical tract (Niquille et al., 2009). Secondly, we performed a bead culture assay in which beads soaked in recombinant FGF protein was embedded in the tissue, this allowed the examination of the molecular and cellular response of the tissue to the FGF protein. The use of protein soaked beads in this way provides a method for focal delivery of recombinant protein at a specific position, in contrast to bath application which exposes all tissue to the protein equally. This mimics the situation in-vivo where a morphogen (such as FGF17) is expressed at a particular anatomical position and then diffuses through the tissue. This technique could be used to explore the response to a number of different recombinant proteins or pharmacological agents.
Materials and Reagents
Materials
Animals
Mice used in our original study ubiquitously express τGFP and have been described previously (Pratt et al., 2000). All mice were maintained on a CD-1 background (Charles River, strain code: 022). Mice used for timed matings were aged between 6 and 24 weeks.
Equipment
Procedure
文章信息
版权信息
© 2020 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Readers should cite both the Bio-protocol article and the original research article where this protocol was used:
分类
神经科学 > 发育 > 外植体培养
发育生物学 > 细胞信号传导 > 配体
细胞生物学 > 细胞信号传导 > 发育
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