球体
自愈水凝胶
共焦显微镜
聚二甲基硅氧烷
细胞包封
共焦
聚乙二醇
三维细胞培养
材料科学
生物物理学
生物医学工程
PEG比率
细胞外基质
肿瘤微环境
纳米技术
化学
细胞
体外
细胞生物学
高分子化学
光学
肿瘤细胞
生物
医学
生物化学
物理
有机化学
财务
经济
癌症研究
作者
Joseph Bruns,S H Saidi Nejat,A.J. Faber,Silviya Petrova Zustiak
摘要
Three-dimensional (3D) encapsulation of spheroids is crucial to adequately replicate the tumor microenvironment for optimal cell growth. Here, we designed an in vitro 3D glioblastoma model for spheroid encapsulation to mimic the tumor extracellular microenvironment. First, we formed square pyramidal microwell molds using polydimethylsiloxane. These microwell molds were then used to fabricate tumor spheroids with tightly controlled sizes from 50-500 μm. Once spheroids were formed, they were harvested and encapsulated in polyethylene glycol (PEG)-based hydrogels. PEG hydrogels are a versatile platform for spheroid encapsulation, as hydrogel properties such as stiffness, degradability, and cell adhesiveness can be tuned independently. Here, we used a representative soft (~8 kPa) hydrogel to encapsulate glioblastoma spheroids. Finally, a method to stain and image spheroids was developed to obtain high-quality images via confocal microscopy. Due to the dense spheroid core and relatively sparse periphery, imaging can be difficult, but using a clearing solution and confocal optical sectioning helps alleviate these imaging difficulties. In summary, we show a method to fabricate uniform spheroids, encapsulate them in PEG hydrogels and perform confocal microscopy on the encapsulated spheroids to study spheroid growth and various cell-matrix interactions.
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