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 PMID:19363146  

Characterization of Nkx6-2-derived neocortical interneuron lineages.

Vitor H Sousa | Goichi Miyoshi | Jens Hjerling-Leffler | Theofanis Karayannis | Gord Fishell
Cerebral cortex (New York, N.Y. : 1991) | 2009

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 loss-of-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.

Pubmed ID: 19363146

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Associated grants

  • Agency: NIMH NIH HHS, United States
    Id: R01MH068469
  • Agency: NINDS NIH HHS, United States
    Id: R01NS039007

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Progen (tool)

RRID:SCR_006726

Antibody and density gradient media supplier.

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C57BL/6J (tool)

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129P2/OlaHsd (tool)

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laboratory mouse with name 129P2/OlaHsd from MGI.

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