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Low proliferative and high migratory activity in the area of Brachyury expressing mesoderm progenitor cells in the gastrulating rabbit embryo.

机译:短胃兔胚中表达Brachyury的中胚层祖细胞的增殖和迁移活性低。

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General mechanisms initiating the gastrulation process in early animal development are still elusive, not least because embryonic morphology differs widely among species. The rabbit embryo is revived here as a model to study vertebrate gastrulation, because its relatively simple morphology at the appropriate stages makes interspecific differences and similarities particularly obvious between mammals and birds. Three approaches that centre on mesoderm specification as a key event at the start of gastrulation were chosen. (1) A cDNA fragment encoding 212 amino acids of the rabbit Brachyury gene was cloned by RT-PCR and used as a molecular marker for mesoderm progenitors. Whole-mount in situ hybridisation revealed single Brachyury-expressing cells in the epiblast at 6.2 days post conception, i.e. several hours before the first ingressing mesoderm cells can be detected histologically. With the anterior marginal crescent as a landmark, these mesoderm progenitors are shown to lie in a posterior quadrant of the embryonic disc, which we call the posterior gastrula extension (PGE), for reasons established during the following functional analysis. (2) Vital dye (DiI) labelling in vitro suggests that epiblast cells arrive in the PGE from anterior parts of the embryonic disc and then move within this area in a complex pattern of posterior, centripetal and anterior directions to form the primitive streak. (3) BrdU labelling shows that proliferation is reduced in the PGE, while the remaining anterior part of the embryonic disc contains several areas of increased proliferation. These results reveal similarities with the chick with respect to Brachyury expression and cellular migration. They differ, however, in that local differences in proliferation are not seen in the pre-streak avian embryo. Rather, rabbit epiblast cells start mesoderm differentiation in a way similar to Drosophila, where a transient downregulation of proliferation initiates mesoderm differentiation and, hence, gastrulation.
机译:在动物早期发育中启动胃化过程的一般机制仍然难以捉摸,尤其是因为物种之间的胚胎形态差异很大。此处将兔胚胎作为研究脊椎动物胃气化的模型进行了复活,因为在适当阶段其相对简单的形态使得种间差异和相似性在哺乳动物和鸟类之间尤为明显。选择了三种以中胚层规格为中心的方法,将其作为开始胃气管形成的关键事件。 (1)通过RT-PCR克隆了兔Brachyury基因的212个氨基酸的cDNA片段,并将其用作中胚层祖细胞的分子标记。整个原位杂交显示在受孕后6.2天即在组织学上可以检测到第一个进入的中胚层细胞之前的几个小时,在上皮细胞中表达了表达Brachyury的细胞。这些中胚层祖细胞以前缘新月形为标志,显示其位于胚盘的后象限中,我们称其为后胃延展性(PGE),原因是在以下功能分析中确定了原因。 (2)活体染料(DiI)的体外标记表明,上皮细胞从胚盘的前部进入PGE,然后以后,向心和前方向的复杂模式在该区域内移动,从而形成原始条纹。 (3)BrdU标记显示PGE的增殖减少,而胚盘的其余前部包含几个增殖增加的区域。这些结果揭示了与小鸡在Brachyury表达和细胞迁移方面的相似性。但是,它们的区别在于,在条纹前的鸟类胚胎中看不到增殖的局部差异。而是,兔表皮细胞以与果蝇相似的方式开始中胚层分化,在果蝇中,短暂的增殖下调会启动中胚层分化,进而引起中胚层分化。

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