Emerging principles and models of human primordial germ cell development.

IF 3.6 2区 生物学 Q1 DEVELOPMENTAL BIOLOGY
Development Pub Date : 2025-09-01 Epub Date: 2025-09-11 DOI:10.1242/dev.204968
Navin B Ramakrishna, João Pedro Alves-Lopes, Wolfram H Gruhn
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引用次数: 0

Abstract

In humans, primordial germ cells (hPGCs) are the earliest precursors committed to forming sperm or egg. During the first trimester of embryonic development, hPGCs undergo extensive epigenetic reprogramming and are subject to fitness selection, laying the foundation for future gametogenesis and normal embryonic development. During these processes, hPGCs interact with dynamic microenvironments that remain incompletely understood. Recent advances in transcriptomic and epigenetic profiling have revealed signalling cues and regulatory mechanisms governing hPGC development in human embryos, complemented by insights from non-human primate models. In parallel, pluripotent stem cell-based systems that model hPGC differentiation have emerged in the past decade as valuable platforms for mechanistic studies and form the basis of ongoing efforts to establish human in vitro gametogenesis. In this Review, we discuss the microenvironmental and epigenetic changes accompanying hPGC specification, migration and gonadal development up to week 10 of embryogenesis. Building on these insights, we examine current model systems for recapitulating hPGC development, and highlight the mechanistic understandings they have enabled.

人类原始生殖细胞发育的新原理和模型。
在人类中,原始生殖细胞(hPGCs)是最早形成精子或卵子的前体。在胚胎发育的前三个月,hPGCs经历了广泛的表观遗传重编程,并接受了适应度选择,为未来配子发生和正常胚胎发育奠定了基础。在这些过程中,高效液相色谱与动态微环境相互作用,这些微环境仍然不完全清楚。转录组学和表观遗传学分析的最新进展揭示了人类胚胎中控制hPGC发育的信号线索和调节机制,并辅以非人类灵长类动物模型的见解。与此同时,在过去的十年中,以多能干细胞为基础的模拟hPGC分化的系统已经成为机制研究的宝贵平台,并为建立人类体外配子发生的持续努力奠定了基础。在这篇综述中,我们讨论了伴随hPGC规格、迁移和性腺发育到胚胎发生第10周的微环境和表观遗传变化。在这些见解的基础上,我们研究了当前的模型系统,以概括hPGC的发展,并强调了它们所实现的机制理解。
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来源期刊
Development
Development 生物-发育生物学
CiteScore
6.70
自引率
4.30%
发文量
433
审稿时长
3 months
期刊介绍: Development’s scope covers all aspects of plant and animal development, including stem cell biology and regeneration. The single most important criterion for acceptance in Development is scientific excellence. Research papers (articles and reports) should therefore pose and test a significant hypothesis or address a significant question, and should provide novel perspectives that advance our understanding of development. We also encourage submission of papers that use computational methods or mathematical models to obtain significant new insights into developmental biology topics. Manuscripts that are descriptive in nature will be considered only when they lay important groundwork for a field and/or provide novel resources for understanding developmental processes of broad interest to the community. Development includes a Techniques and Resources section for the publication of new methods, datasets, and other types of resources. Papers describing new techniques should include a proof-of-principle demonstration that the technique is valuable to the developmental biology community; they need not include in-depth follow-up analysis. The technique must be described in sufficient detail to be easily replicated by other investigators. Development will also consider protocol-type papers of exceptional interest to the community. We welcome submission of Resource papers, for example those reporting new databases, systems-level datasets, or genetic resources of major value to the developmental biology community. For all papers, the data or resource described must be made available to the community with minimal restrictions upon publication. To aid navigability, Development has dedicated sections of the journal to stem cells & regeneration and to human development. The criteria for acceptance into these sections is identical to those outlined above. Authors and editors are encouraged to nominate appropriate manuscripts for inclusion in one of these sections.
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