T-type Calcium Channel Regulation of Neural Tube Closure and EphrinA/EPHA Expression

被引:33
|
作者
Abdul-Wajid, Sarah [1 ,2 ]
Morales-Diaz, Heidi [1 ,2 ]
Khairallah, Stephanie M. [1 ,2 ]
Smith, William C. [1 ,2 ]
机构
[1] Univ Calif Santa Barbara, Dept Mol Cell & Dev Biol, Santa Barbara, CA 93106 USA
[2] Univ Calif Santa Barbara, Neurosci Res Inst, Santa Barbara, CA 93106 USA
来源
CELL REPORTS | 2015年 / 13卷 / 04期
关键词
MOUSE SPINAL NEURULATION; CIONA-INTESTINALIS; APICAL CONSTRICTION; ASCIDIAN EMBRYOS; TYROSINE KINASES; CREST CELLS; PLATE; VOLTAGE; GENES; CHORDATE;
D O I
10.1016/j.celrep.2015.09.035
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A major class of human birth defects arise from aberrations during neural tube closure (NTC). We report on a NTC signaling pathway requiring T-type calcium channels (TTCCs) that is conserved between primitive chordates (Ciona) and Xenopus. With loss of TTCCs, there is a failure to seal the anterior neural folds. Accompanying loss of TTCCs is an upregulation of EphrinA effectors. Ephrin signaling is known to be important in NTC, and ephrins can affect both cell adhesion and repulsion. In Ciona, ephrinA-d expression is downregulated at the end of neurulation, whereas, with loss of TTCC, ephrinA-d remains elevated. Accordingly, overexpression of ephrinA-d phenocopied TTCC loss of function, while overexpression of a dominant-negative Ephrin receptor was able to rescue NTC in a Ciona TTCC mutant. We hypothesize that signaling through TTCCs is necessary for proper anterior NTC through downregulation of ephrins, and possibly elimination of a repulsive signal.
引用
收藏
页码:829 / 839
页数:11
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