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太平洋刺虾的卵裂和原肠胚形成:内陷伴随着定向细胞分裂。

Cleavage and gastrulation in the shrimp Sicyonia ingentis: invagination is accompanied by oriented cell division.

作者信息

Hertzler P L, Clark W H

机构信息

Department of Zoology, University of California, Davis and Bodega Marine Laboratory 94923.

出版信息

Development. 1992 Sep;116(1):127-40. doi: 10.1242/dev.116.Supplement.127.

Abstract

Embryos of the penaeoidean shrimp Sicyonia ingentis were examined at intervals during cleavage and gastrulation using antibodies to beta-tubulin and DNA and laser scanning confocal microscopy. Cleavage occurred in a regular pattern within four domains corresponding to the 4-cell-stage blastomeres and resulted in two interlocking bands of cells, each with similar spindle orientations, around a central blastocoel. Right-left asymmetry was evident at the 32-cell-stage, and mirror-image embryos occurred in a 50:50 ratio. Gastrulation was initiated by invagination into the blastocoel at the 62-cell-stage of two mesendoderm cells, which arrested at the 32-cell-stage. Further invagination and expansion of the archenteron during gastrulation was accompanied by rapid and oriented cell division. The archenteron was composed of presumptive naupliar mesoderm and the blastopore was located at the site of the future anus of the nauplius larva. In order to trace cell lineages and determine axial relationships, single 2- and 4-cell-stage blastomeres were microinjected with rhodamine-dextran. The results showed that the mesendoderm cells which initiated gastrulation were derived from the vegetal 2-cell-stage blastomere, which could be distinguished by its slightly larger size and the location of the polar bodies. The mesendoderm cells descended from a single vegetal blastomere of the 4-cell-stage. This investigation provides the first evidence for oriented cell division during gastrulation in a simple invertebrate system. Oriented cell division has previously been discounted as a potential morphogenetic force, and may be a common mechanism of invagination in embryos that begin gastrulation with a relatively small number of cells.

摘要

在对虾科对虾西氏对虾(Sicyonia ingentis)胚胎的卵裂和原肠胚形成过程中,利用抗β-微管蛋白和DNA的抗体以及激光扫描共聚焦显微镜,对其进行了阶段性检查。卵裂在对应于4细胞期卵裂球的四个区域内以规则模式发生,形成了两条相互连锁的细胞带,每条带中的纺锤体方向相似,围绕着一个中央囊胚腔。左右不对称在32细胞期就很明显,镜像胚胎的出现比例为50:50。原肠胚形成始于62细胞期时两个中内胚层细胞内陷进入囊胚腔,这两个细胞在32细胞期就已停滞。原肠胚在原肠胚形成过程中的进一步内陷和扩展伴随着快速且定向的细胞分裂。原肠由预定无节幼体中胚层组成,胚孔位于无节幼体未来肛门的位置。为了追踪细胞谱系并确定轴向关系,对2细胞期和4细胞期的单个卵裂球进行了罗丹明-葡聚糖显微注射。结果表明,启动原肠胚形成的中内胚层细胞源自植物极2细胞期的卵裂球,其可通过稍大的尺寸和极体的位置来区分。中内胚层细胞源自4细胞期单个植物极卵裂球。本研究为简单无脊椎动物系统中原肠胚形成过程中的定向细胞分裂提供了首个证据。此前,定向细胞分裂被认为不是一种潜在的形态发生力,而在以相对少量细胞开始原肠胚形成的胚胎中,它可能是内陷的常见机制。

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