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海胆原始生殖细胞的迁移。

Migration of sea urchin primordial germ cells.

作者信息

Campanale Joseph P, Gökirmak Tufan, Espinoza Jose A, Oulhen Nathalie, Wessel Gary M, Hamdoun Amro

机构信息

Marine Biology Research Division, Scripps Institution of Oceanography, University of California San Diego, La Jolla, California.

出版信息

Dev Dyn. 2014 Jul;243(7):917-27. doi: 10.1002/dvdy.24133. Epub 2014 Apr 30.

Abstract

BACKGROUND

Small micromeres are produced at the fifth cleavage of sea urchin development. They express markers of primordial germ cells (PGCs), and are required for the production of gametes. In most animals, PGCs migrate from sites of formation to the somatic gonad. Here, we investigated whether they also exhibit similar migratory behaviors using live-cell imaging of small micromere plasma membranes.

RESULTS

Early in gastrulation, small micromeres transition from non-motile epithelial cells, to motile quasi-mesenchymal cells. Late in gastrulation, at 43 hr post fertilization (HPF), they are embedded in the tip of the archenteron, but remain motile. From 43-49 HPF, they project numerous cortical blebs into the blastocoel, and filopodia that contact ectoderm. By 54 HPF, they begin moving in the plane of the blastoderm, often in a directed fashion, towards the coelomic pouches. Isolated small micromeres also produced blebs and filopodia.

CONCLUSIONS

Previous work suggested that passive translocation governs some of the movement of small micromeres during gastrulation. Here we show that small micromeres are motile cells that can traverse the archenteron, change position along the left-right axis, and migrate to coelomic pouches. These motility mechanisms are likely to play an important role in their left-right segregation.

摘要

背景

海胆发育的第五次卵裂产生小分裂球。它们表达原始生殖细胞(PGC)的标记物,并且是配子产生所必需的。在大多数动物中,PGC从形成部位迁移到体细胞性腺。在这里,我们使用小分裂球质膜的活细胞成像研究它们是否也表现出类似的迁移行为。

结果

在原肠胚形成早期,小分裂球从非运动性上皮细胞转变为运动性准间充质细胞。在原肠胚形成后期,受精后43小时(HPF),它们嵌入原肠的尖端,但仍保持运动性。在43 - 49 HPF期间,它们向囊胚腔投射许多皮质小泡,并伸出与外胚层接触的丝状伪足。到54 HPF时,它们开始在胚盘平面内移动,通常以定向方式朝向体腔囊移动。分离的小分裂球也产生小泡和丝状伪足。

结论

先前的研究表明,被动转运控制着原肠胚形成期间小分裂球的一些运动。在这里我们表明,小分裂球是可运动的细胞,它们可以穿过原肠,沿左右轴改变位置,并迁移到体腔囊。这些运动机制可能在它们的左右分离中起重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0be1/4164171/c33662466979/nihms625127f1.jpg

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