4.6 Article

Characterization of Nkx6-2-Derived Neocortical Interneuron Lineages

期刊

CEREBRAL CORTEX
卷 19, 期 -, 页码 I1-I10

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/cercor/bhp038

关键词

genetic fate mapping; interganglionic sulcus; loss of function; mouse genetics; whole-cell physiology

资金

  1. National Institutes of Health-National Institute [R01MH068469, R01NS039007]
  2. Simons Foundation
  3. Swedish Brain Foundation

向作者/读者索取更多资源

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.

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