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本文引用的文献

1
Single-cell analyses of Crohn's disease tissues reveal intestinal intraepithelial T cells heterogeneity and altered subset distributions.克罗恩病组织的单细胞分析揭示了肠道上皮内T细胞的异质性及亚群分布的改变。
Nat Commun. 2021 Mar 26;12(1):1921. doi: 10.1038/s41467-021-22164-6.
2
Single-Cell Sequencing of Developing Human Gut Reveals Transcriptional Links to Childhood Crohn's Disease.单细胞测序揭示了人类肠道发育与儿童克罗恩病的转录关联。
Dev Cell. 2020 Dec 21;55(6):771-783.e5. doi: 10.1016/j.devcel.2020.11.010. Epub 2020 Dec 7.
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Organoid-based modeling of intestinal development, regeneration, and repair.基于类器官的肠道发育、再生和修复模型。
Cell Death Differ. 2021 Jan;28(1):95-107. doi: 10.1038/s41418-020-00665-z. Epub 2020 Nov 18.
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Spatiotemporal Gradient and Instability of Wnt Induce Heterogeneous Growth and Differentiation of Human Intestinal Organoids.Wnt的时空梯度与不稳定性诱导人肠道类器官的异质性生长和分化。
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Cytoskeletal Organization and Cell Polarity in the Pathogenesis of Crohn's Disease.细胞骨架组织和细胞极性在克罗恩病发病机制中的作用。
Clin Rev Allergy Immunol. 2021 Apr;60(2):164-174. doi: 10.1007/s12016-020-08795-5.
6
The endothelium, a key actor in organ development and hPSC-derived organoid vascularization.内皮细胞,器官发育和 hPSC 衍生类器官血管化的关键因素。
J Biomed Sci. 2020 May 22;27(1):67. doi: 10.1186/s12929-020-00661-y.
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Single-cell transcriptome analysis reveals differential nutrient absorption functions in human intestine.单细胞转录组分析揭示了人类肠道中不同的营养吸收功能。
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8
Long-Term Culture Captures Injury-Repair Cycles of Colonic Stem Cells.长期培养捕获结肠干细胞的损伤-修复周期。
Cell. 2019 Nov 14;179(5):1144-1159.e15. doi: 10.1016/j.cell.2019.10.015. Epub 2019 Nov 7.
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Organoids-on-a-chip.类器官芯片。
Science. 2019 Jun 7;364(6444):960-965. doi: 10.1126/science.aaw7894.
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Self-organization and symmetry breaking in intestinal organoid development.肠类器官发育中的自组织和对称破缺。
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类器官培养的几何工程化以增强器官发生。

Geometric engineering of organoid culture for enhanced organogenesis in a dish.

机构信息

Department of Bioengineering, University of Pennsylvania, Philadelphia, PA, USA.

NSF Science and Technology Center for Engineering Mechanobiology, University of Pennsylvania, Philadelphia, PA, USA.

出版信息

Nat Methods. 2022 Nov;19(11):1449-1460. doi: 10.1038/s41592-022-01643-8. Epub 2022 Oct 24.

DOI:10.1038/s41592-022-01643-8
PMID:36280722
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10027401/
Abstract

Here, we introduce a facile, scalable engineering approach to enable long-term development and maturation of organoids. We have redesigned the configuration of conventional organoid culture to develop a platform that converts single injections of stem cell suspensions to radial arrays of organoids that can be maintained for extended periods without the need for passaging. Using this system, we demonstrate accelerated production of intestinal organoids with significantly enhanced structural and functional maturity, and their continuous development for over 4 weeks. Furthermore, we present a patient-derived organoid model of inflammatory bowel disease (IBD) and its interrogation using single-cell RNA sequencing to demonstrate its ability to reproduce key pathological features of IBD. Finally, we describe the extension of our approach to engineer vascularized, perfusable human enteroids, which can be used to model innate immune responses in IBD. This work provides an immediately deployable platform technology toward engineering more realistic organ-like structures in a dish.

摘要

在这里,我们介绍了一种简便、可扩展的工程方法,使类器官能够长期发育和成熟。我们重新设计了传统类器官培养的配置,开发了一种平台,可将干细胞悬浮液的单次注射转化为类器官的放射状阵列,无需传代即可长时间维持。使用该系统,我们展示了肠道类器官的加速生产,其结构和功能成熟度显著提高,并可连续发育超过 4 周。此外,我们提出了一种炎症性肠病(IBD)的患者来源类器官模型,并使用单细胞 RNA 测序对其进行了检测,以证明其重现 IBD 关键病理特征的能力。最后,我们描述了将我们的方法扩展到工程化血管化、可灌注的人类类肠的方法,可用于模拟 IBD 中的固有免疫反应。这项工作提供了一种可立即部署的平台技术,用于在培养皿中构建更逼真的类器官样结构。