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EphA-ephrin-A signaling is critically involved in region-specific apoptosis during early brain development

机译:EphA-ephrin-A信号传导在早期大脑发育过程中关键参与区域特异性凋亡

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摘要

EphAs and ephrin-As have been implicated in the morphogenesis of the developing brain. We found that EphA7 and ephrin-A5 are coexpressed in the dorsal midline (DM) of the diencephalon and anterior mesencephalon. Interestingly, programmed cell death (PCD) of the neural epithelial cells normally found in this region was reduced in ephrin-A5-ephrin-A2 dual-deficient embryos. In contrast, in vivo expression of ephrin-A5-Fc or full-length ephrin-A5 strongly induced apoptosis in neural epithelial cells and was accompanied by severe brain malformation during embryonic development. Expression of ephrinA5-Fc correlated with apoptosis of EphA7-expressing cells, whereas null mutation of ephrin-A5 resulted in the converse phenotype. Importantly, null mutation of caspase-3 or endogenous ephrin-A5 attenuated the PCD induced by ectopically overexpressed ephrin-A5. Together, our results suggest that brain region-specific PCD may occur in a region where EphAs cluster with neighboring ephrin-As through cell-cell contact.
机译:EphAs和ephrin-As与发育中的大脑的形态发生有关。我们发现EphA7和ephrin-A5在间脑和前中脑的背中线(DM)中共表达。有趣的是,在ephrin-A5-ephrin-A2双缺陷胚胎中,通常在该区域发现的神经上皮细胞的程序性细胞死亡(PCD)减少了。相比之下,ephrin-A5-Fc或全长ephrin-A5的体内表达强烈诱导神经上皮细胞凋亡,并伴随着胚胎发育过程中的严重脑畸形。 ephrinA5-Fc的表达与表达EphA7的细胞的凋亡相关,而ephrin-A5的无效突变导致了相反的表型。重要的是,caspase-3或内源性ephrin-A5的无效突变减弱了异位过表达ephrin-A5诱导的PCD。总之,我们的结果表明,脑区域特定的PCD可能发生在EphA通过细胞与细胞接触与邻近的ephrin-A聚集的区域。

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