球体
三维细胞培养
细胞生物学
基底膜
粘附
细胞培养
生物物理学
化学
微流控
显微镜
细胞
生物医学工程
生物
病理
材料科学
纳米技术
医学
生物化学
遗传学
有机化学
作者
Sarah M. Kirsh,Sydney A. Pascetta,James Uniacke
出处
期刊:Methods in molecular biology
日期:2023-01-01
卷期号:: 273-285
被引量:5
标识
DOI:10.1007/978-1-0716-2914-7_17
摘要
Spheroids enable the study of tumors and tumor hypoxia using a more representative model of the physiological environment compared to 2D cell culture. Spheroids can be grown in a cell suspension or when adhered to a solid scaffold. The spheroid formation method used is dependent on cell type. Here we describe the most common spheroid formation methods, including hanging drop, low adhesion plates, hydrogel, micropatterned plates, and microfluidics. After spheroids are formed, they can be used for drug treatment trials and analyzed using Western Blots, qPCR, and microscopy. Microscopy can then be used to measure the invasiveness of cells when a basement membrane is added to spheroids and for monitoring changes in the proliferation, quiescent, and necrotic zones of spheroids.
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