New findings on the orientation of the mouse anterior-posterior (A-P) axis before and during the initiation of gastrulation using a more refined embryo staging

IF 2.3 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Xenia Hadjikypri , Christina Theofanous , Antonia Christodoulidi, Pantelis Georgiades
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引用次数: 0

Abstract

A clinically significant event of early mammalian embryogenesis is the generation and early development of the anterior-posterior (A-P) axis, the imaginary line along which the structures from head to tail will form. This axis not only appears before gastrulation but is also oriented in a specific way in relation to the long and short diameters of the bilaterally symmetric epiblast. In mice, the most widely used mammalian in vivo model of early embryogenesis, the A-P axis is normally aligned with the long epiblast diameter by the early streak (ES) stage, a time during early gastrulation around embryonic day 6.5 (E6.5). Incorrect orientation of the A-P axis by the ES stage, that is, being aligned with the short epiblast diameter, leads to failure in completing gastrulation and results in embryo death soon after. Knowing the orientation of this axis from when it forms before gastrulation (around E5.5) until just before the ES stage is crucial for: (a) understanding the ill-defined factors involved in its formation and early development since they must be spatially related to it, and (b) providing explanations for the underlying mechanism when it is incorrectly orientated. However, the orientation of the A-P axis in pre-ES embryos of the E5.5-E6.5 period remains unclear. Specifically, although it is thought that this axis initially aligns with the short epiblast diameter and subsequently changes its orientation to become aligned with the long diameter by an unidentified pre-gastrulation stage before the ES stage, this proposition remains unresolved. This is largely due to the lack of clearly defined morphological criteria for staging certain periods of pre-ES mouse embryos (especially when the A-P axis initiates and when gastrulation begins prior to the ES stage), which are a prerequisite for identifying A-P axis orientation at specific pre-ES stages. Furthermore, although the orientation of an extraembryonic trophoblast asymmetry, specifically the tilt of the ectoplacental cone (EPC), coincides with that of the A-P axis by the ES stage, it is unknown whether such an association also exists at pre-gastrulation stages during A-P axis formation. Knowing this would exclude or implicate this trophoblast asymmetry as an upstream factor in orientating the A-P axis when it forms. To address these issues, we established a more refined embryo staging for the E5.5-E6.5 period using a novel combination of live morphological criteria and used it to examine the orientation of the A-P axis and that of the EPC tilt at specific stages. First, contrary to current thinking, we show that when the A-P axis first appears at our newly described anterior visceral endoderm-1 (AVE-1) and AVE-2 stages, it aligns with the long epiblast diameter in all embryos. This orientation is maintained in most embryos at all subsequent pre-gastrulation stages, specifically at our AVE-3 and pre-streak stages (the remaining embryos of these stages had this axis aligned with the short epiblast diameter). Second, we identified for the first time the pre-ES stage when gastrulation initiates, which we named the nascent streak (NS) stage, and further subdivided it into NS-1 and NS-2. At variance with current belief, we provide evidence that the earliest stage just before the ES stage when all embryos align their A-P axis with the long epiblast diameter is not a pre-gastrulation stage, but the NS-2 stage (at NS-1, most but not all embryos had this A-P axis orientation). Third, we implicate the EPC tilt as a possible extraembryonic factor in promoting correct A-P axis orientation, as this tilt exists before the AVE-1 stage and its orientation coincided with that of the A-P axis in all embryos at AVE-1, AVE-2 and ES stages and almost all embryos at AVE-3, pre-streak and NS stages. Overall, our work: (a) identified the previously unresolved orientation of the mouse A-P axis within the epiblast before the ES stage during the E5.5-E6.5 period; (b) provides an alternative explanation for when this axis is incorrectly oriented by the ES stage, namely, its defective alignment with the short epiblast diameter by this stage could be due to its failure to align with the long epiblast diameter from the time of its formation; and (c) implicates the pre-existing orientation of the EPC tilt as a possible factor in orientating the newly formed A-P axis.

利用更精细的胚胎分期对小鼠胃形成开始之前和期间的前后(A-P)轴定向的新发现
哺乳动物早期胚胎发育的一个重要临床事件是前-后(A-P)轴的产生和早期发育。这条轴线不仅在胃形成之前就已出现,而且与两侧对称的上胚层的长径和短径有特定的方向。小鼠是应用最广泛的哺乳动物体内早期胚胎发生模型,在小鼠的早期条纹(ES)阶段,即胚胎 6.5 天(E6.5)左右的早期胃形成过程中,A-P 轴通常与上胚层的长直径对齐。在 ES 阶段,A-P 轴的方向不正确,即与短上胚层直径对齐,会导致无法完成胃形成,并导致胚胎很快死亡。了解从胃形成前(约 E5.5)到 ES 期前这一轴线的方向对以下方面至关重要:(a) 了解参与其形成和早期发育的不明确因素,因为这些因素必须在空间上与之相关;(b) 当其方向不正确时,为其潜在机制提供解释。然而,E5.5-E6.5 期前 ES 胚胎中 A-P 轴的方向仍不清楚。具体来说,尽管有观点认为该轴最初与短上胚层直径对齐,随后在 ES 阶段之前的一个不明前胃管阶段改变方向与长直径对齐,但这一观点仍未得到解决。这主要是由于缺乏明确定义的形态学标准来对 ES 前小鼠胚胎的某些时期进行分期(尤其是 A-P 轴何时开始以及 ES 期前的胃形成何时开始),而这些标准是确定 A-P 轴在特定 ES 期前阶段方向的先决条件。此外,虽然胚胎外滋养层不对称的方向,特别是外胚层锥体(EPC)的倾斜方向与 ES 阶段的 A-P 轴方向一致,但这种关联是否也存在于 A-P 轴形成过程中的胃形成前阶段尚不得而知。了解这一点将排除或暗示滋养层细胞不对称是 A-P 轴形成时定向的上游因素。为了解决这些问题,我们使用新颖的活体形态学标准组合为 E5.5-E6.5 期建立了更精细的胚胎分期,并用它来检验 A-P 轴和 EPC 倾斜在特定阶段的方向。首先,与目前的想法相反,我们发现当 A-P 轴首次出现在我们新描述的前内脏内胚层-1(AVE-1)和 AVE-2 阶段时,它在所有胚胎中都与长上胚层直径对齐。在随后的所有胃膜前阶段,特别是在我们的 AVE-3 和匍匐前阶段,大多数胚胎都保持了这一方向(在这些阶段的其余胚胎中,这一轴线与短上胚层直径对齐)。其次,我们首次确定了胃形成开始的前 ES 阶段,将其命名为新生条纹(NS)阶段,并进一步将其细分为 NS-1 和 NS-2。与目前的观点不同,我们提供的证据表明,在 ES 阶段之前,所有胚胎都将其 A-P 轴与长的上胚层直径对齐的最早阶段并不是胃形成前阶段,而是 NS-2 阶段(在 NS-1 阶段,大多数胚胎但不是所有胚胎都有这种 A-P 轴方向)。第三,我们认为 EPC 倾斜可能是促进正确 A-P 轴定向的胚外因素,因为这种倾斜存在于 AVE-1 阶段之前,而且在 AVE-1、AVE-2 和 ES 阶段的所有胚胎以及在 AVE-3、妊娠前期和 NS 阶段的几乎所有胚胎中,这种倾斜的方向都与 A-P 轴的方向一致。总之,我们的工作:(a) 确定了小鼠 A-P 轴在 E5.5-E6.5 期 ES 阶段之前的胚胎上胚层中先前未解决的方向;(b) 提供了一个小鼠 A-P 轴的发育模式。5阶段;(b) 为该轴在ES阶段的错误定向提供了另一种解释,即该轴在该阶段与短上胚层直径对齐的缺陷可能是由于它在形成时未能与长上胚层直径对齐;(c) 将EPC倾斜的先前存在的定向牵涉到新形成的A-P轴的定向的一个可能因素。
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来源期刊
Biochemistry and Biophysics Reports
Biochemistry and Biophysics Reports Biochemistry, Genetics and Molecular Biology-Biophysics
CiteScore
4.60
自引率
0.00%
发文量
191
审稿时长
59 days
期刊介绍: Open access, online only, peer-reviewed international journal in the Life Sciences, established in 2014 Biochemistry and Biophysics Reports (BB Reports) publishes original research in all aspects of Biochemistry, Biophysics and related areas like Molecular and Cell Biology. BB Reports welcomes solid though more preliminary, descriptive and small scale results if they have the potential to stimulate and/or contribute to future research, leading to new insights or hypothesis. Primary criteria for acceptance is that the work is original, scientifically and technically sound and provides valuable knowledge to life sciences research. We strongly believe all results deserve to be published and documented for the advancement of science. BB Reports specifically appreciates receiving reports on: Negative results, Replication studies, Reanalysis of previous datasets.
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