Department of Cell and Developmental Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA; Cell and Molecular Biology Graduate Program, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Department of Cell and Developmental Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA; Department of Bioengineering, School of Engineering and Applied Science, University of Pennsylvania, Philadelphia, PA 19104, USA; Cell and Molecular Biology Graduate Program, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA; Lead Contact, USA.
Semin Cell Dev Biol. 2023 May 30;141:43-49. doi: 10.1016/j.semcdb.2022.04.016. Epub 2022 May 5.
Early embryogenesis requires rapid division of pluripotent blastomeres, regulated genome activation, precise spatiotemporal signaling to pattern cell fate, and morphogenesis to shape primitive tissue architectures. The complexity of this process has inspired researchers to move beyond simple genetic perturbation into engineered devices and synthetic biology tools to permit temporal and spatial manipulation of the control systems guiding development. By precise alteration of embryo organization, it is now possible to advance beyond basic analytical strategies and directly test the sufficiency of models for developmental regulation. Separately, advances in micropatterning and embryoid culture have facilitated the bottom-up construction of complex embryo tissues allowing ex vivo systems to recapitulate even later stages of development. Embryos fertilized and grown ex vivo offer an excellent opportunity to exogenously perturb fundamental pathways governing embryogenesis. Here we review the technologies developed to thermally modulate the embryo cell cycle, and optically regulate morphogen and signaling pathways in space and time, specifically in the blastula embryo. Additionally, we highlight recent advances in cell patterning in two and three dimensions that have helped reveal the self-organizing properties and gene regulatory networks guiding early embryo organization.
早期胚胎发生需要多能胚细胞快速分裂、基因组激活调控、精确的时空信号来规划细胞命运,以及形态发生来塑造原始组织架构。这一过程的复杂性激发了研究人员超越简单的遗传干扰,采用工程设备和合成生物学工具来实现对指导发育的控制系统的时空操纵。通过对胚胎组织的精确改变,现在可以超越基本的分析策略,直接测试发育调控模型的充分性。另外,微图案化和类胚体培养的进展促进了复杂胚胎组织的自下而上构建,使体外系统能够再现甚至更晚的发育阶段。体外受精和生长的胚胎为外源干扰胚胎发生的基本途径提供了极好的机会。在这里,我们回顾了开发的技术,这些技术可以在热上调节胚胎细胞周期,并在空间和时间上精确调节形态发生素和信号通路,特别是在囊胚胚胎中。此外,我们还重点介绍了在二维和三维空间中进行细胞图案化的最新进展,这些进展有助于揭示指导早期胚胎组织的自组织特性和基因调控网络。