Using embryo models to understand the development and progression of embryonic lineages: a focus on primordial germ cell development.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-03-13 DOI:10.1159/000538275
Ignacio Rodriguez-Polo, Naomi Moris
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Abstract

Background: Recapitulating mammalian cell type differentiation in vitro promises to improve our understanding of how these processes happen in vivo, while bringing additional prospects for biomedical applications. The establishment of stem cell-derived embryo models and embryonic organoids, which have experienced explosive growth over the last few years, open new avenues for research due to their scale, reproducibility, and accessibility. Embryo models mimic various developmental stages, exhibit different degrees of complexity, and can be established across species. Since embryo models exhibit multiple lineages organised spatially and temporally, they are likely to provide cellular niches that, to some degree, recapitulate the embryonic setting and enable "co-development" between cell types and neighbouring populations. One example where this is already apparent is in the case of primordial germ cell-like cells (PGCLCs).

Summary: While directed differentiation protocols enable the efficient generation of high PGCLC numbers, embryo models provide an attractive alternative as they enable the study of interactions of PGCLCs with neighbouring cells, alongside the regulatory molecular and biophysical mechanisms of PGC competency. Additionally, some embryo models can recapitulate post-specification stages of PGC development (including migration or gametogenesis), mimicking the inductive signals pushing PGCLCs to mature and differentiate, and enabling the study of PGCLC development across stages. Therefore, in vitro models may allow us to address questions of cell type differentiation, and PGC development specifically, that have hitherto been out of reach with existing systems.

Key message: This review evaluates the current advances in stem cell-based embryo models, with a focus on their potential to model cell type-specific differentiation in general, and in particular to address open questions in PGC development and gametogenesis.

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利用胚胎模型了解胚胎系的发育和进展:重点关注原始生殖细胞的发育。
背景:体外重现哺乳动物细胞类型分化有望提高我们对这些过程在体内如何发生的理解,同时为生物医学应用带来更多前景。干细胞衍生胚胎模型和胚胎器官组织的建立在过去几年中经历了爆炸式增长,由于其规模、可重复性和可获得性,为研究开辟了新途径。胚胎模型模拟不同的发育阶段,表现出不同程度的复杂性,并且可以跨物种建立。由于胚胎模型在空间和时间上表现出多系组织,它们很可能提供细胞龛位,在一定程度上再现胚胎环境,实现细胞类型和相邻群体之间的 "共同发育"。总结:虽然定向分化方案能有效地产生大量 PGCLC,但胚胎模型提供了一种有吸引力的替代方案,因为它们能研究 PGCLC 与邻近细胞的相互作用,以及 PGC 能力的分子和生物物理调控机制。此外,一些胚胎模型还能再现PGC发育的规范化后阶段(包括迁移或配子发生),模拟促使PGCLC成熟和分化的诱导信号,从而研究PGCLC的跨阶段发育。因此,体外模型可以让我们解决细胞类型分化,特别是PGC发育的问题,而这些问题迄今为止是现有系统无法解决的:这篇综述评估了以干细胞为基础的胚胎模型的当前进展,重点是它们在模拟细胞类型特异性分化方面的潜力,特别是在解决PGC发育和配子发生方面的未决问题方面的潜力。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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