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使用微图案化人类多能干细胞对二维原肠胚样结构和外胚层集落进行命运模式塑造。

Fate-Patterning of 2D Gastruloids and Ectodermal Colonies Using Micropatterned Human Pluripotent Stem Cells.

作者信息

Britton George, Chhabra Sapna, Massey Joseph, Warmflash Aryeh

机构信息

Systems, Synthetic, and Physical Biology Graduate Program, Department of Biosciences, Department of Bioengineering, Rice University, Houston, TX, USA.

Department of Biosciences, Rice University, Houston, TX, USA.

出版信息

Methods Mol Biol. 2021;2258:119-130. doi: 10.1007/978-1-0716-1174-6_9.

Abstract

In the developing mammalian embryo, intercellular signaling allows cells to self-organize to create spatial patterns of different cell fates. This process is challenging to study because of the difficulty of observing or manipulating embryos on the spatial and temporal scales required. In vitro models can provide a complement to in vivo systems for addressing these issues. These models are also the only windows we have into early human development. Here we provide protocols for two systems based on differentiating human pluripotent stem cells in micropatterned colonies on defined size and shape. The first model replicates the patterning of the germ layers at gastrulation, while the second replicates the medial-lateral patterning of the ectoderm. These systems allow study of how signaling underlies self-organized patterning at stages of development which are otherwise inaccessible.

摘要

在发育中的哺乳动物胚胎中,细胞间信号传导使细胞能够自我组织,以创建不同细胞命运的空间模式。由于难以在所需的空间和时间尺度上观察或操纵胚胎,因此研究这一过程具有挑战性。体外模型可以为解决这些问题的体内系统提供补充。这些模型也是我们了解人类早期发育的唯一窗口。在这里,我们提供了两种基于在确定大小和形状的微图案化菌落中分化人类多能干细胞的系统的方案。第一个模型复制了原肠胚形成时胚层的模式,而第二个模型复制了外胚层的中侧模式。这些系统能够研究信号传导如何在发育阶段为自我组织模式提供基础,而这些阶段在其他情况下是无法研究的。

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