基因和致畸原诱导的早期中枢神经系统发育缺陷。

Scanning electron microscopy Pub Date : 1986-01-01
K S O'Shea
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引用次数: 0

摘要

参与原始神经系统组织发生的事件包括对细胞形状变化、细胞迁移、细胞间和细胞间基质相互作用的精确控制。这些事件的协调过程导致神经褶皱的升高,它们在背中线的重合和融合,形成初级神经管。随后是第二系列的细胞迁移和重排(统称为次级神经发育),导致尾神经管延长。在简要考虑了参与神经发育的机制后,基因或致畸原诱导的这些事件的扰动的影响被提出和回顾。新的数据提出了延迟斑点突变胚胎的神经发育和改变间充质或神经上皮基层成分对初级和次级神经发育的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gene and teratogen induced defects of early central nervous system development.

The events involved in the histogenesis of the primitive nervous system involve precise control over cell shape changes, cellular migrations, cell-cell and cell-extracellular matrix interactions. The coordinated procession of these events results in the elevation of the neural folds, and their apposition and fusion in the dorsal midline, forming the primary neural tube. This is followed by a second series of cellular migrations and rearrangements (collectively called secondary neurulation) which result in lengthening of the caudal neural tube. After a brief consideration of the mechanisms involved in neurulation, the effects of gene or teratogen induced perturbations of these events are presented and reviewed. New data are presented on neurulation in the delayed Splotch mutant embryo and on the effects of altering mesenchymal or neuroepithelial basal lamina constituents on primary and secondary neurulation.

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