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生成具有包被基底膜的 3D 肿瘤球体用于侵袭研究。

Generation of 3D Tumor Spheroids with Encapsulating Basement Membranes for Invasion Studies.

机构信息

Cell Biology Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, Maryland.

出版信息

Curr Protoc Cell Biol. 2020 Jun;87(1):e105. doi: 10.1002/cpcb.105.

Abstract

In the past, in vitro studies of invasion and tumor progression were performed primarily using cancer cells cultured on a flat, two-dimensional (2D) surface in a monolayer. In recent years, however, many studies have demonstrated differences in cell signaling and cell migration between 2D and 3D cell cultures. Traditional 2D monolayer cancer cell invasion models do not fully recapitulate 3D cell-to-cell and cell-to-extracellular matrix interactions that in vivo models can provide. Moreover, although in vivo animal models are irreplaceable for studying tumor biology and metastasis, they are costly, time-consuming, and impractical for answering preliminary questions. Thus, emergent and evolving 3D spheroid cell culture models have changed the way we study tumors and their interactions with their surrounding extracellular matrix. In the case of breast cancer, metastasis of breast cancer tumors results in high mortality rates, and thus development of robust cell culture models that are reproducible and practical for studying breast cancer progression is important for ultimately developing preventatives for cancer metastasis. This article provides a set of protocols for generating uniform spheroids with a thin sheet of basement membrane for studying the initial invasion of mammary epithelial cells into a surrounding collagen-rich extracellular matrix. Details are provided for generating 3D spheroids with a basement membrane, polymerizing collagen I, embedding the spheroids in the 3D collagen gel, and immunostaining the spheroids for invasion studies. Published 2020. U.S. Government. Basic Protocol 1: Growth of uniformly sized tumor spheroids with an encapsulating basement membrane Basic Protocol 2: Polymerization and embedding of tumor spheroids in a 3D type I collagen gel Alternate Protocol: Embedding of tumor spheroids in collagen gels using a sandwich method Basic Protocol 3: Fixing and immunostaining of tumor spheroids embedded in 3D collagen gels.

摘要

过去,体外侵袭和肿瘤进展的研究主要是在单层培养的平面二维(2D)表面上使用癌细胞进行的。然而,近年来,许多研究表明,2D 和 3D 细胞培养中细胞信号传导和细胞迁移存在差异。传统的 2D 单层癌细胞侵袭模型不能完全再现体内模型提供的 3D 细胞间和细胞与细胞外基质的相互作用。此外,尽管体内动物模型对于研究肿瘤生物学和转移是不可替代的,但它们成本高、耗时且不切实际,无法回答初步问题。因此,新兴的 3D 球体细胞培养模型改变了我们研究肿瘤及其与周围细胞外基质相互作用的方式。在乳腺癌的情况下,乳腺癌肿瘤的转移导致高死亡率,因此开发可重复且实用的稳健细胞培养模型对于研究乳腺癌进展非常重要,最终可以开发出预防癌症转移的方法。本文提供了一组生成带有薄基底膜的均匀球体的方案,用于研究乳腺上皮细胞最初侵入富含胶原蛋白的周围细胞外基质。详细介绍了生成带有基底膜的 3D 球体、聚合 I 型胶原蛋白、将球体嵌入 3D 胶原凝胶中和对球体进行免疫染色以进行侵袭研究的过程。发表于 2020 年。美国政府。基本方案 1:用包被的基底膜生长均匀大小的肿瘤球体基本方案 2:在 3D I 型胶原蛋白凝胶中聚合和嵌入肿瘤球体替代方案:使用三明治方法将肿瘤球体嵌入胶原凝胶中基本方案 3:固定和免疫染色嵌入 3D 胶原凝胶中的肿瘤球体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d426/9285559/a1cb6ea69a8b/CPCB-87-0-g002.jpg

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