首页> 外文期刊>Journal of Neurocytology: A Journal of Cellular Neurobiology >Further studies on cortical tangential migration in wild type and Pax-6 mutant mice.
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Further studies on cortical tangential migration in wild type and Pax-6 mutant mice.

机译:在野生型和Pax-6突变小鼠中皮质切向迁移的进一步研究。

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In this study we present new data concerning the tangential migration from the medial and lateral ganglionic eminences (MGE and LGE) to the cerebral cortex during development. We have used Calbindin as a useful marker to follow the itinerary of tangential migratory cells during early developmental stages in wild-type and Pax-6 homozygous mutant mice. In the wild-type mice, at early developmental stages, migrating cells advance through the intermediate zone (IZ) and preplate (PP). At more advanced stages, migrating cells were present in the subplate (SP) and cortical plate (CP) to reach the entire developing cerebral cortex. We found that, in the homozygous mutant mice (Pax-6(Sey-Neu)/Pax-6(Sey-Neu)), this tangential migration is severely affected at early developmental stages: migrating cells were absent in the IZ, which were only found some days later, suggesting that in the mutant mice, there is a temporal delay in tangential migration. We have also defined some possible mechanisms to explain certainmigratory routes from the basal telencephalon to the cerebral cortex. We describe the existence of two factors, which we consider to be essential for the normal migration; the first one is the cell adhesion molecule PSA-NCAM, whose role in other migratory systems is well known. The second factor is Robo-2, whose expression delimits a channel for the passage of migratory cells from the basal telencephalon to the cerebral cortex.
机译:在这项研究中,我们提供了有关在发育过程中从内侧和外侧神经节隆起(MGE和LGE)切向迁移到大脑皮层的新数据。我们已经使用Calbindin作为有用的标记,在野生型和Pax-6纯合突变小鼠的早期发育阶段追踪切向迁移细胞的路线。在野生型小鼠中,在早期发育阶段,迁移的细胞穿过中间区(IZ)和预平板(PP)前进。在更高级的阶段,迁移细胞存在于亚板(SP)和皮质板(CP)中,到达整个发育中的大脑皮层。我们发现,在纯合突变小鼠(Pax-6(Sey-Neu)/ Pax-6(Sey-Neu))中,这种切向迁移在发育早期受到严重影响:在IZ中缺少迁移细胞,几天后才发现,这表明在突变小鼠中,切向迁移存在时间延迟。我们还定义了一些可能的机制来解释从基底端脑到大脑皮质的某些迁移途径。我们描述了两个因素的存在,我们认为这对于正常迁移至关重要。第一个是细胞粘附分子PSA-NCAM,其在其他迁移系统中的作用是众所周知的。第二个因素是Robo-2,它的表达限制了迁徙细胞从基底端脑到大脑皮质的通道。

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