Migratory behavior of presumptive interneurons is affected by AMPA receptor activation in slice cultures of embryonic mouse neocortex

Masato Yozu, Hidenori Tabata, Norbert König, Kazunori Nakajima

Research output: Contribution to journalArticlepeer-review

16 Citations (Scopus)

Abstract

It has been reported that functional α-amino-3-hydroxy-5-methyl- isoxazolpro-prionic acid (AMPA) receptors permeable to calcium are already expressed by tangentially migrating prospective interneurons in the developing rodent cerebral cortex. However, the role of these receptors is not yet fully understood. To examine the effect of activation of AMPA receptors on tangential migration, we exposed migrating prospective interneurons derived from the medial ganglionic eminence (MGE) to AMPA in slice cultures and performed time lapse imaging. In the neocortex, a subpopulation of MGE-derived cells stopped migration or changed the direction of migration in response to AMPA in a dose-dependent manner. In contrast, neither MGE-derived cells migrating in the subcortical territory nor radially migrating cells in the neocortex were affected by exposure to AMPA. Transfection of dominant-negative AMPA receptor subunit GluR1 to the tangentially migrating cells prevented the effects of AMPA on migration. This study provides evidence that the activation of AMPA receptors can directly affect tangential migration in the neocortical part of telencephalic slice cultures.

Original languageEnglish
Pages (from-to)105-116
Number of pages12
JournalDevelopmental Neuroscience
Volume30
Issue number1-3
DOIs
Publication statusPublished - 2007 Dec

Keywords

  • AMPA
  • Cortical development
  • Electroporation
  • GABAergic interneurons
  • Glutamate
  • Medial ganglionic eminence
  • Tangential migration

ASJC Scopus subject areas

  • Neurology
  • Developmental Neuroscience

Fingerprint

Dive into the research topics of 'Migratory behavior of presumptive interneurons is affected by AMPA receptor activation in slice cultures of embryonic mouse neocortex'. Together they form a unique fingerprint.

Cite this