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利用时空 Wnt 信号在类器官模型中高效分化肠干细胞。

Leveraging Temporal Wnt Signal for Efficient Differentiation of Intestinal Stem Cells in an Organoid Model.

机构信息

Institute for Regenerative Medicine, Shanghai East Hospital, Frontier Science Center for Stem Cell Research, School of Life Sciences and Technology, Tongji University, Shanghai, China.

Institute of Biophysics, Chinese Academy of Sciences, Beijing, China.

出版信息

Stem Cells Dev. 2024 Jan;33(1-2):11-26. doi: 10.1089/scd.2023.0186. Epub 2023 Nov 20.

Abstract

The homeostasis of the intestinal epithelium heavily relies on the self-renewal and differentiation of intestinal stem cells (ISCs). Although the orchestration of these processes by signaling pathways such as the Wnt, BMP, Notch, and MAPK signals has been extensively studied, the dynamics of their regulation remains unclear. Our study explores how the Wnt signaling pathway temporally regulates the differentiation of ISCs into various cell types in an intestinal organoid system. We report that the duration of Wnt exposure following Notch pathway inactivation significantly influences the differentiation direction of intestinal epithelial cells toward multiple secretory cell types, including goblet cells, enteroendocrine cells (EECs), and Paneth cells. This temporal regulation of Wnt signaling adds another layer of complexity to the combination of niche signals that govern cell fate. By manipulating this temporal signal, we have developed optimized protocols for the efficient in vitro differentiation of ISCs into EECs and goblet cells. These findings provide critical insights into the dynamic regulation of ISC differentiation and offer a robust platform for future investigations into intestinal biology and potential therapeutic applications.

摘要

肠道上皮细胞的稳态很大程度上依赖于肠道干细胞(ISCs)的自我更新和分化。尽管 Wnt、BMP、Notch 和 MAPK 信号等信号通路对这些过程的协调作用已经得到了广泛研究,但它们的调控动态仍不清楚。我们的研究探讨了 Wnt 信号通路如何在肠道类器官系统中从时间上调节 ISC 向各种细胞类型的分化。我们报告称,Notch 通路失活后 Wnt 暴露的持续时间显著影响肠道上皮细胞向多种分泌细胞类型(包括杯状细胞、肠内分泌细胞(EECs)和潘氏细胞)分化的方向。Wnt 信号的这种时间调节为调控细胞命运的小生境信号的组合增加了另一层复杂性。通过操纵这种时间信号,我们已经开发出了优化的 ISC 体外分化为 EEC 和杯状细胞的方案。这些发现为 ISC 分化的动态调控提供了重要的见解,并为未来的肠道生物学和潜在治疗应用的研究提供了一个强大的平台。

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