Abstract
Ventral telencephalic progenitors expressing the homeodomain transcription factor Nkx6-2 have been shown to give rise to a multitude of cortical interneuron subtypes usually associated with origin in either the medial ganglionic eminence or the caudal ganglionic eminence. The function of Nkx6-2 in directing the fate of those progenitors has, however, not been thoroughly analyzed. We used a combination of genetic inducible fate mapping and in vivo lossof-function to analyze the requirement of Nkx6-2 in determining the fate of cortical interneurons. We have found that interneuron subtypes are born with a characteristic temporal pattern. Furthermore, we extend the characterization of interneurons from the Nkx6-2 lineage through the application of electrophysiological methods. Analysis of these populations in Nkx6-2 null mice suggests that there is a small and partially penetrant loss of delayed non-fast spiking somatostatin/calretinin double positive cortical interneurons in the absence of Nkx6-2 gene function.
Original language | English (US) |
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Pages (from-to) | i1-i10 |
Journal | Cerebral Cortex |
Volume | 19 |
Issue number | SUPPL. 1 |
DOIs | |
State | Published - Jul 2009 |
Keywords
- Genetic fate mapping
- Interganglionic sulcus
- Loss of function
- Mouse genetics
- Whole-cell physiology
ASJC Scopus subject areas
- Cognitive Neuroscience
- Cellular and Molecular Neuroscience