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分析经肠黏膜神经胶质细胞条件培养基分离后的鼠类肠类器官培养物。

Analysis of mouse intestinal organoid culture with conditioned media isolated from mucosal enteric glial cells.

机构信息

Program in Developmental & Stem Cell Biology, The Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.

Department of Molecular Genetics, University of Toronto, Toronto, ON M5S 1A8, Canada.

出版信息

STAR Protoc. 2022 Apr 28;3(2):101351. doi: 10.1016/j.xpro.2022.101351. eCollection 2022 Jun 17.

Abstract

This protocol describes the isolation and culture of 3D intestinal crypt organoids with stromal niche cells. We show a murine organoid culture system that utilizes conditioned media isolated from primary, mucosal enteric glial cell culture. We describe three assays of analyzing this organoid culture: flow cytometry, gene expression, and organoid morphology analyses. This protocol can also be used to study the mechanisms of stem cell interaction with other stromal niche cell types such as mesenchymal cells and innate immune cells. For complete details on the use and execution of this protocol, please refer to Baghdadi et al. (2021).

摘要

本方案描述了带有基质巢细胞的 3D 肠隐窝类器官的分离和培养。我们展示了一种利用从原代、黏膜肠胶质细胞培养物中分离的条件培养基的鼠类类器官培养系统。我们描述了分析这种类器官培养物的三种方法:流式细胞术、基因表达和类器官形态分析。该方案还可用于研究干细胞与其他基质巢细胞类型(如间充质细胞和固有免疫细胞)相互作用的机制。有关使用和执行本方案的完整详细信息,请参阅 Baghdadi 等人(2021 年)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0aad/9062428/54b71a8e9d51/fx1.jpg

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