Tlx3 and Tlx1 are post-mitotic selector genes determining glutamatergic over GABAergic cell fates

被引:277
作者
Cheng, LP
Arata, A
Mizuguchi, R
Qian, Y
Karunaratne, A
Gray, PA
Arata, S
Shirasawa, S
Bouchard, M
Luo, P
Chen, CL
Busslinger, M
Goulding, M
Onimaru, H
Ma, QF
机构
[1] Harvard Univ, Sch Med, Dana Farber Canc Inst, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Neurobiol, Boston, MA 02115 USA
[3] RIKEN, Brain Sci Inst, Lab Memory & Learning, Wako, Saitama 3510198, Japan
[4] Salk Inst Biol Studies, Mol Neurobiol Lab, La Jolla, CA 92037 USA
[5] Showa Univ, Ctr Biotechnol, Tokyo 1428555, Japan
[6] Int Med Ctr Japan, Dept Pathol, Shinjuku Ku, Tokyo 1628655, Japan
[7] Res Inst Mol Pathol, A-1030 Vienna, Austria
[8] Showa Univ, Sch Med, Dept Physiol, Tokyo 1428555, Japan
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nn1221
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Glutamatergic and GABAergic neurons mediate much of the excitatory and inhibitory neurotransmission, respectively, in the vertebrate nervous system. The process by which developing neurons select between these two cell fates is poorly understood. Here we show that the homeobox genes Tlx3 and Tlx1 determine excitatory over inhibitory cell fates in the mouse dorsal spinal cord. First, we found that Tlx3 was required for specification of, and expressed in, glutamatergic neurons. Both generic and region-specific glutamatergic markers, including VGLUT2 and the AMPA receptor Gria2, were absent in Tlx mutant dorsal horn. Second, spinal GABAergic markers were derepressed in Tlx mutants, including Pax2 that is necessary for GABAergic differentiation, Gad1/2 and Viaat that regulate GABA synthesis and transport, and the kainate receptors Grik2/3. Third, ectopic expression of Tlx3 was sufficient to suppress GABAergic differentiation and induce formation of glutamatergic neurons. Finally, excess GABA-mediated inhibition caused dysfunction of central respiratory circuits in Tlx3 mutant mice.
引用
收藏
页码:510 / 517
页数:8
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