Signaling mechanisms that direct cell fate specification and morphogenesis in human embryonic stem cells-based models of human gastrulation.

IF 3.4 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Blerta Stringa, Lilianna Solnica-Krezel
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引用次数: 0

Abstract

During mammalian gastrulation, a mass of pluripotent cells surrounded by extraembryonic tissues differentiates into germ layers, mesoderm, endoderm, and ectoderm. The three germ layers are then organized into a body plan with organ rudiments via morphogenetic gastrulation movements of emboly, epiboly, convergence, and extension. Emboly is the most conserved gastrulation movement, whereby mesodermal and endodermal progenitors undergo epithelial-to-mesenchymal transition (EMT) and move via a blastopore/primitive streak beneath the ectoderm. Decades of embryologic, genetic, and molecular studies in invertebrates and vertebrates, delineated a BMP > WNT > NODAL signaling cascade underlying mesoderm and endoderm specification. Advances have been made in the research animals in understanding the cellular and molecular mechanisms underlying gastrulation morphogenesis. In contrast, little is known about human gastrulation, which occurs in utero during the third week of gestation and its investigations face ethical and methodological limitations. This is changing with the unprecedented progress in modeling aspects of human development, using human pluripotent stem cells (hPSCs), including embryonic stem cells (hESC)-based embryo-like models (SCEMs). In one approach, hESCs of various pluripotency are aggregated to self-assemble into structures that resemble pre-implantation or post-implantation embryo-like structures that progress to early gastrulation, and some even reach segmentation and neurulation stages. Another approach entails coaxing hESCs with biochemical signals to generate germ layers and model aspects of gastrulation morphogenesis, such as EMT. Here, we review the recent advances in understanding signaling cascades that direct germ layers specification and the early stages of gastrulation morphogenesis in these models. We discuss outstanding questions, challenges, and opportunities for this promising area of developmental biology.

基于人类胚胎干细胞的人类胚胎发育模型中指导细胞命运规范和形态发生的信号机制。
在哺乳动物的胃形成过程中,被胚外组织包围的大量多能细胞分化成胚层、中胚层、内胚层和外胚层。然后,这三个胚层通过萌发、外胚层分化、聚合和延伸等形态发生的气生运动组织成具有器官雏形的体表。胚胎溶解是最保守的胃形成运动,中胚层和内胚层的祖细胞在此过程中经历上皮到间质的转变(EMT),并通过外胚层下面的胚泡孔/原始条纹移动。数十年来对无脊椎动物和脊椎动物进行的胚胎学、遗传学和分子研究发现,BMP > WNT > NODAL 信号级联是中胚层和内胚层规格化的基础。研究动物在了解胃形成形态发生的细胞和分子机制方面取得了进展。相比之下,人们对人类的胃形成知之甚少,因为人类的胃形成发生在妊娠第三周的子宫内,其研究面临着伦理和方法上的限制。随着利用人体多能干细胞(hPSCs),包括胚胎干细胞(hESC)为基础的类胚胎模型(SCEMs),在人类发育建模方面取得了前所未有的进展,这种情况正在发生改变。一种方法是将不同多能性的hESC细胞聚集在一起,自我组装成类似植入前或植入后胚胎样结构的结构,这些结构可发展到早期胃发育,有些甚至达到分节和神经发育阶段。另一种方法是利用生化信号诱导 hESCs 生成胚层,并模拟胃形成形态发生的各个方面,如 EMT。在此,我们回顾了最近在了解这些模型中指导胚层规格化和胃形成形态发生早期阶段的信号级联方面取得的进展。我们还讨论了这一前景广阔的发育生物学领域的未决问题、挑战和机遇。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.70
自引率
0.00%
发文量
94
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