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类器官作为研究 Notch 信号在肠道上皮稳态和肠道癌症中的模型系统。

Organoids as a Model System for Studying Notch Signaling in Intestinal Epithelial Homeostasis and Intestinal Cancer.

机构信息

Department of Pathology, School of Medicine, Case Western Reserve University, Cleveland, Ohio.

Department of Pathology, School of Medicine, Case Western Reserve University, Cleveland, Ohio.

出版信息

Am J Pathol. 2022 Oct;192(10):1347-1357. doi: 10.1016/j.ajpath.2022.06.008. Epub 2022 Jun 22.

DOI:10.1016/j.ajpath.2022.06.008
Abstract

Organoid culture is an approach that allows three-dimensional growth for stem cells to self-organize and develop multicellular structures. Intestinal organoids have been widely used to study cellular or molecular processes in stem cell and cancer research. These cultures possess the ability to maintain cellular complexity as well as recapitulate many properties of the human intestinal epithelium, thereby providing an ideal in vitro model to investigate cellular and molecular signaling pathways. These include, but are not limited to, the mechanisms required for maintaining balanced populations of epithelial cells. Notch signaling is one of the major pathways of regulating stem cell functions in the gut, driving proliferation and controlling cell fate determination. Notch also plays an important role in regulating tumor progression and metastasis. Understanding how Notch pathway regulates epithelial regeneration and differentiation by using intestinal organoids is critical for studying both homeostasis and pathogenesis of intestinal stem cells that can lead to discoveries of new targets for drug development to treat intestinal diseases. In addition, use of patient-derived organoids can provide effective personalized medicine. This review summarizes the current literature regarding epithelial Notch pathways regulating intestinal homeostasis and regeneration, highlighting the use of organoid cultures and their potential therapeutic applications.

摘要

类器官培养是一种允许干细胞进行三维生长的方法,使它们能够自我组织并发育成多细胞结构。肠类器官已被广泛用于研究干细胞和癌症研究中的细胞或分子过程。这些培养物具有保持细胞复杂性的能力,并能重现人类肠道上皮的许多特性,因此提供了一个理想的体外模型来研究细胞和分子信号通路。这些通路包括但不限于维持上皮细胞平衡群体所需的机制。Notch 信号通路是调节肠道干细胞功能的主要通路之一,它驱动增殖并控制细胞命运决定。Notch 信号通路在调节肿瘤进展和转移中也起着重要作用。通过使用肠类器官来理解 Notch 通路如何调节上皮细胞的再生和分化,对于研究肠道干细胞的稳态和发病机制至关重要,这可能会发现开发治疗肠道疾病的新药的新靶点。此外,使用患者来源的类器官可以提供有效的个性化药物。本综述总结了关于上皮 Notch 通路调节肠道稳态和再生的当前文献,强调了类器官培养及其潜在治疗应用。

相似文献

1
Organoids as a Model System for Studying Notch Signaling in Intestinal Epithelial Homeostasis and Intestinal Cancer.类器官作为研究 Notch 信号在肠道上皮稳态和肠道癌症中的模型系统。
Am J Pathol. 2022 Oct;192(10):1347-1357. doi: 10.1016/j.ajpath.2022.06.008. Epub 2022 Jun 22.
2
MET Signaling Mediates Intestinal Crypt-Villus Development, Regeneration, and Adenoma Formation and Is Promoted by Stem Cell CD44 Isoforms.MET 信号转导介导肠道隐窝-绒毛发育、再生和腺瘤形成,并受干细胞 CD44 同种型的促进。
Gastroenterology. 2017 Oct;153(4):1040-1053.e4. doi: 10.1053/j.gastro.2017.07.008. Epub 2017 Jul 14.
3
Establishment of intestinal organoid cultures modeling injury-associated epithelial regeneration.建立模拟损伤相关上皮再生的肠类器官培养物。
Cell Res. 2021 Mar;31(3):259-271. doi: 10.1038/s41422-020-00453-x. Epub 2021 Jan 8.
4
Leveraging Temporal Wnt Signal for Efficient Differentiation of Intestinal Stem Cells in an Organoid Model.利用时空 Wnt 信号在类器官模型中高效分化肠干细胞。
Stem Cells Dev. 2024 Jan;33(1-2):11-26. doi: 10.1089/scd.2023.0186. Epub 2023 Nov 20.
5
Interleukin‑22 regulates the homeostasis of the intestinal epithelium during inflammation.白细胞介素-22 在炎症期间调节肠道上皮细胞的内稳态。
Int J Mol Med. 2019 Apr;43(4):1657-1668. doi: 10.3892/ijmm.2019.4092. Epub 2019 Feb 7.
6
Three-Dimensional Culture of Murine Colonic Crypts to Study Intestinal Stem Cell Function Ex Vivo.鼠结直肠隐窝的三维培养以研究肠干细胞的体外功能。
J Vis Exp. 2022 Oct 11(188). doi: 10.3791/64534.
7
Brief summary of the current protocols for generating intestinal organoids.当前用于生成肠道类器官的方案简要概述。
Dev Growth Differ. 2018 Aug;60(6):387-392. doi: 10.1111/dgd.12559. Epub 2018 Jul 23.
8
Ap4 is rate limiting for intestinal tumor formation by controlling the homeostasis of intestinal stem cells.Ap4 通过控制肠道干细胞的稳态来限制肠道肿瘤的形成。
Nat Commun. 2018 Sep 3;9(1):3573. doi: 10.1038/s41467-018-06001-x.
9
Intestinal epithelial organoids: regeneration and maintenance of the intestinal epithelium.肠上皮类器官:肠道上皮的再生和维持。
Curr Opin Genet Dev. 2022 Oct;76:101977. doi: 10.1016/j.gde.2022.101977. Epub 2022 Sep 1.
10
Notch Signaling Regulates Lgr5 Olfactory Epithelium Progenitor/Stem Cell Turnover and Mediates Recovery of Lesioned Olfactory Epithelium in Mouse Model.Notch 信号调节嗅上皮祖/干细胞的更替,并介导小鼠模型损伤嗅上皮的修复。
Stem Cells. 2018 Aug;36(8):1259-1272. doi: 10.1002/stem.2837. Epub 2018 May 8.

引用本文的文献

1
Multi-Omics Profiles of Small Intestine Organoids in Reaction to Breast Milk and Different Infant Formula Preparations.母乳及不同婴儿配方奶对小肠类器官的多组学影响
Nutrients. 2024 Sep 2;16(17):2951. doi: 10.3390/nu16172951.
2
NOTCH3 and Pulmonary Arterial Hypertension.NOTCH3 与肺动脉高压。
Int J Mol Sci. 2024 Jun 6;25(11):6248. doi: 10.3390/ijms25116248.
3
Circular RNAs: characteristics, functions, mechanisms, and potential applications in thyroid cancer.环状 RNA:在甲状腺癌中的特征、功能、机制及潜在应用。

本文引用的文献

1
Acquisition of NOTCH dependence is a hallmark of human intestinal stem cell maturation.获得 NOTCH 依赖性是人类肠干细胞成熟的标志。
Stem Cell Reports. 2022 May 10;17(5):1138-1153. doi: 10.1016/j.stemcr.2022.03.007. Epub 2022 Apr 7.
2
High Yap and Mll1 promote a persistent regenerative cell state induced by Notch signaling and loss of p53.High Yap 和 Mll1 通过 Notch 信号诱导和 p53 缺失促进持久的再生细胞状态。
Proc Natl Acad Sci U S A. 2021 Jun 1;118(22). doi: 10.1073/pnas.2019699118.
3
Organoid-based modeling of intestinal development, regeneration, and repair.
Clin Transl Oncol. 2024 Apr;26(4):808-824. doi: 10.1007/s12094-023-03324-0. Epub 2023 Oct 21.
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.
4
AKT-dependent NOTCH3 activation drives tumor progression in a model of mesenchymal colorectal cancer.AKT 依赖性 NOTCH3 激活驱动间充质型结直肠癌细胞模型中的肿瘤进展。
J Exp Med. 2020 Oct 5;217(10). doi: 10.1084/jem.20191515.
5
Cycling Stem Cells Are Radioresistant and Regenerate the Intestine.成体干细胞具有辐射抗性并能再生肠道。
Cell Rep. 2020 Jul 28;32(4):107952. doi: 10.1016/j.celrep.2020.107952.
6
Colorectal cancer statistics, 2020.2020 年结直肠癌统计数据。
CA Cancer J Clin. 2020 May;70(3):145-164. doi: 10.3322/caac.21601. Epub 2020 Mar 5.
7
Use of organoids to study regenerative responses to intestinal damage.利用类器官研究肠道损伤的再生反应。
Am J Physiol Gastrointest Liver Physiol. 2019 Dec 1;317(6):G845-G852. doi: 10.1152/ajpgi.00346.2018. Epub 2019 Oct 7.
8
Epithelial NOTCH Signaling Rewires the Tumor Microenvironment of Colorectal Cancer to Drive Poor-Prognosis Subtypes and Metastasis.上皮 NOTCH 信号通路重编程结直肠癌肿瘤微环境以驱动预后不良亚型和转移。
Cancer Cell. 2019 Sep 16;36(3):319-336.e7. doi: 10.1016/j.ccell.2019.08.003.
9
Cellular Plasticity of Defa4-Expressing Paneth Cells in Response to Notch Activation and Intestinal Injury.Notch 激活和肠道损伤时 Defa4 表达的潘氏细胞的细胞可塑性。
Cell Mol Gastroenterol Hepatol. 2019;7(3):533-554. doi: 10.1016/j.jcmgh.2018.11.004. Epub 2018 Nov 27.
10
Atoh1 secretory progenitors possess renewal capacity independent of Lgr5 cells during colonic regeneration.Atoh1 分泌祖细胞在结肠再生过程中具有独立于 Lgr5 细胞的自我更新能力。
EMBO J. 2019 Feb 15;38(4). doi: 10.15252/embj.201899984. Epub 2019 Jan 11.