In utero electroporation: Assay system for migration of cerebral cortical neurons

Hidenori Tabata, Kazunori Nakajima

Research output: Chapter in Book/Report/Conference proceedingChapter

1 Citation (Scopus)

Abstract

During the development of the cerebral cortex, the majority of cortical neurons are generated in the ventricular zone (VZ) facing the lateral ventricle and then migrate toward the pial surface to form the highly organized 6-layered cerebral cortex. Detailed profiles of these processes and their molecular mechanisms had been largely unknown because of the absence of an efficient assay system. The in vivo electroporation system was initially devised for use within chick embryos (Funahashi et al., 1999; Itasaki et al., 1999; Momose et al., 1999; Muramatsu et al., 1997), and we and other groups have used that system as a basis for developing an in utero electroporation system, which allows plasmid DNA to be introduced into cortical progenitor cells in developing mouse embryos in the uterus (Fukuchi-Shimogori and Grove, 2001; Saito and Nakatsuji, 2001; Tabata and Nakajima, 2001; Takahashi et al., 2002). In utero electroporation of other sites in the brain, including the hippocampus (Navarro-Quiroga et al., 2007), cerebral basal ganglia (Borrell et al., 2005; Nakahira et al., 2006), cortical hem (Takiguchi-Hayashi et al., 2004), and dorsal thalamus (Bonnin et al., 2007), has recently been reported. Introducing green fluorescent protein (GFP) enables the entire processes of migration and layer formation to be visualized (Ajioka and Nakajima, 2005; Sasaki et al., 2008; Tabata and Nakajima, 2002, 2003), and the role of any gene involved in these processes can be easily assessed by overexpressing the proteins or their mutants (Ohshima et al., 2007), or by knocking down the genes by the RNA interference technique (Bai et al., 2003). Furthermore, the Tet-On/Off system and/or other plasmid- vector-based technologies will expand the potential of the analyses. In this section we review the principles and methods of gene transfer into the cortical wall of mouse embryos by means of the in utero electroporation system.

Original languageEnglish
Title of host publicationElectroporation and Sonoporation in Developmental Biology
PublisherSpringer Japan
Pages143-152
Number of pages10
ISBN (Print)9784431094265
DOIs
Publication statusPublished - 2009

Fingerprint

Neurons
Assays
On-off control systems
Plasmids
Genes
Proteins
Gene transfer
Green Fluorescent Proteins
RNA
Brain
DNA

ASJC Scopus subject areas

  • Materials Science(all)
  • Chemistry(all)

Cite this

Tabata, H., & Nakajima, K. (2009). In utero electroporation: Assay system for migration of cerebral cortical neurons. In Electroporation and Sonoporation in Developmental Biology (pp. 143-152). Springer Japan. https://doi.org/10.1007/978-4-431-09427-2_14

In utero electroporation : Assay system for migration of cerebral cortical neurons. / Tabata, Hidenori; Nakajima, Kazunori.

Electroporation and Sonoporation in Developmental Biology. Springer Japan, 2009. p. 143-152.

Research output: Chapter in Book/Report/Conference proceedingChapter

Tabata, H & Nakajima, K 2009, In utero electroporation: Assay system for migration of cerebral cortical neurons. in Electroporation and Sonoporation in Developmental Biology. Springer Japan, pp. 143-152. https://doi.org/10.1007/978-4-431-09427-2_14
Tabata H, Nakajima K. In utero electroporation: Assay system for migration of cerebral cortical neurons. In Electroporation and Sonoporation in Developmental Biology. Springer Japan. 2009. p. 143-152 https://doi.org/10.1007/978-4-431-09427-2_14
Tabata, Hidenori ; Nakajima, Kazunori. / In utero electroporation : Assay system for migration of cerebral cortical neurons. Electroporation and Sonoporation in Developmental Biology. Springer Japan, 2009. pp. 143-152
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