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对鸡胚神经管形成过程中微丝作用的重新审视。

A reexamination of the role of microfilaments in neurulation in the chick embryo.

作者信息

Schoenwolf G C, Folsom D, Moe A

机构信息

Department of Anatomy, University of Utah, School of Medicine, Salt Lake City 84132.

出版信息

Anat Rec. 1988 Jan;220(1):87-102. doi: 10.1002/ar.1092200111.

Abstract

Formation of wedge-shaped neuroepithelial cells, owing to the constriction of apical bands of microfilaments, is widely believed to play a major part in bending of the neural plate. Although cell "wedging" occurs during neurulation, its exact role in bending is unknown. Likewise, although microfilament bands occupy the apices of neuroepithelial cells, whether these structures are required for cell wedging is unknown. Finally, although it is known that cytochalasins interfere with neurulation, it is unknown whether they block shaping or furrowing of the neural plate, or elevation, convergence, or fusion of the neural folds. The purpose of this study was to reexamine the role of microfilaments in neurulation in the chick embryo. Embryos were treated with cytochalasin D (CD) to depolymerize microfilaments and were analyzed 4-24 hr later. CD did not prevent neural plate shaping, median neural plate furrowing, wedging of median neuroepithelial cells, or neural fold elevation. However, dorsolateral neural plate furrowing, wedging of dorsolateral neuroepithelial cells, and convergence of the neural folds were blocked frequently by CD. In addition, neural folds always failed to fuse across the midline in embryos treated with CD, and neural crest cell migration was prevented. These data indicate that only the later aspects of neurulation may require microfilaments, and that certain neuroepithelial cells, particularly those that normally wedge with median furrowing and elevation of the neural folds, become (and remain) wedge-shaped in the absence of apical microfilament bands. Thus, microfilament-mediated constriction of neuroepithelial cell apices is not the major force for median neuroepithelial cell wedging and elevation of the chick neural plate. Further studies are needed to localize the motor(s) for these processes.

摘要

由于微丝顶带的收缩而形成楔形神经上皮细胞,人们普遍认为这在神经板弯曲过程中起主要作用。尽管细胞“楔入”发生在神经胚形成期间,但其在弯曲中的确切作用尚不清楚。同样,尽管微丝带占据神经上皮细胞的顶端,但这些结构是否是细胞楔入所必需的尚不清楚。最后,尽管已知细胞松弛素会干扰神经胚形成,但它们是否会阻止神经板的塑形或沟裂,或者神经褶的抬高、汇聚或融合尚不清楚。本研究的目的是重新审视微丝在鸡胚神经胚形成中的作用。用细胞松弛素D(CD)处理胚胎以使微丝解聚,并在4-24小时后进行分析。CD并未阻止神经板塑形、正中神经板沟裂、正中神经上皮细胞楔入或神经褶抬高。然而,背外侧神经板沟裂、背外侧神经上皮细胞楔入以及神经褶的汇聚经常被CD阻断。此外,在用CD处理的胚胎中,神经褶总是无法在中线处融合,并且神经嵴细胞迁移也被阻止。这些数据表明,只有神经胚形成的后期方面可能需要微丝,并且某些神经上皮细胞,特别是那些通常随着神经褶的正中沟裂和抬高而楔入的细胞,在没有顶端微丝带的情况下会变成(并保持)楔形。因此,微丝介导的神经上皮细胞顶端收缩不是鸡神经板正中神经上皮细胞楔入和抬高的主要力量。需要进一步研究来定位这些过程的驱动因素。

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