Characterization of Nkx6-2-Derived Neocortical Interneuron Lineages

被引:215
作者
Sousa, Vitor H. [1 ]
Miyoshi, Goichi [1 ]
Hjerling-Leffler, Jens [1 ]
Karayannis, Theofailis [1 ]
Fishell, Gord [1 ]
机构
[1] NYU, Smilow Res Ctr, Neurosci Program, New York, NY 10016 USA
基金
美国国家卫生研究院;
关键词
genetic fate mapping; interganglionic sulcus; loss of function; mouse genetics; whole-cell physiology; SITE-SPECIFIC RECOMBINATION; CAUDAL GANGLIONIC EMINENCE; CENTRAL-NERVOUS-SYSTEM; RAT FRONTAL-CORTEX; VISUAL-CORTEX; PROGENITOR DOMAINS; GABAERGIC NEURONS; COLUMN IDENTITY; CRE RECOMBINASE; MOTOR-NEURON;
D O I
10.1093/cercor/bhp038
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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.
引用
收藏
页码:I1 / I10
页数:10
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