CoupTFI Interacts with Retinoic Acid Signaling during Cortical Development

被引:11
作者
Harrison-Uy, Susan J. [1 ]
Siegenthaler, Julie A. [1 ]
Faedo, Andrea [2 ]
Rubenstein, John L. R. [2 ,3 ,4 ]
Pleasure, Samuel J. [1 ,3 ,4 ]
机构
[1] Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Psychiat, San Francisco, CA USA
[3] Univ Calif San Francisco, Program Neurosci, Eli & Edythe Broad Ctr Regenerat Med & Stem Cell, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Program Dev Biol, Eli & Edythe Broad Ctr Regenerat Med & Stem Cell, San Francisco, CA 94143 USA
来源
PLOS ONE | 2013年 / 8卷 / 03期
基金
美国国家卫生研究院;
关键词
PROMOTER-TRANSCRIPTION FACTORS; NEURAL PROGENITOR CELLS; CAJAL-RETZIUS CELLS; DEVELOPING NEOCORTEX; NUCLEAR RECEPTORS; ORPHAN RECEPTOR; TFI; DIFFERENTIATION; NEUROGENESIS; NEURONS;
D O I
10.1371/journal.pone.0058219
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We examined the role of the orphan nuclear hormone receptor CoupTFI in mediating cortical development downstream of meningeal retinoic acid signaling. CoupTFI is a regulator of cortical development known to collaborate with retinoic acid (RA) signaling in other systems. To examine the interaction of CoupTFI and cortical RA signaling we utilized Foxc1-mutant mice in which defects in meningeal development lead to alterations in cortical development due to a reduction of RA signaling. By analyzing CoupTFI(-)/(-); Foxc1(H/L) double mutant mice we provide evidence that CoupTFI is required for RA rescue of the ventricular zone and the neurogenic phenotypes in Foxc1-mutants. We also found that overexpression of CoupTFI in Foxc1-mutants is sufficient to rescue the Foxc1-mutant cortical phenotype in part. These results suggest that CoupTFI collaborates with RA signaling to regulate both cortical ventricular zone progenitor cell behavior and cortical neurogenesis.
引用
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页数:11
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