期刊
BIOFABRICATION
卷 13, 期 4, 页码 -出版社
IOP PUBLISHING LTD
DOI: 10.1088/1758-5090/ac1ea8
关键词
2D and 3D cell co-culture; cancer cell spheroid; multicellular geometry; tumor cells classification; tumor microenvironment
资金
- National Natural Science Foundation of China [U19A2006, 12132004, 11772088, 11972111, 31900940, 11802056, 31800780, 32071304, 81671821]
- China Postdoctoral Science Foundation [2018M640904, 2019T120831]
- Sichuan Science and Technology Program [2019YJC0183, 2019YJC0184, 2021YJ0130]
- Fundamental Research Funds for the Central Universities [ZYGX2019J117]
- Joint Funds of Center for Engineering Medicine [ZYGX2021YGLH017, ZYGX2021YGLH010, YGX2021YGLH023]
Cell culture systems play a crucial role in biomedical research. 3D cell culture technology is gaining attention for its unique biochemical and biophysical properties compared to traditional 2D cell cultures, especially in cancer and stem cell research.
Cell culture systems are indispensable in vitro tools for biomedical research. Although conventional two-dimensional (2D) cell cultures are still used for most biomedical and biological studies, the three-dimensional (3D) cell culture technology attracts increasing attention from researchers, especially in cancer and stem cell research. Due to the different spatial structures, cells in 2D and 3D cultures exhibit different biochemical and biophysical phenotypes. Therefore, a new platform with both 2D and 3D cell cultures is needed to bridge the gap between 2D and 3D cell-based assays. Here, a simultaneous 2D and 3D cell culture array system was constructed by microprinting technology, in which cancer cells exhibited heterozygous geometry structures with both 2D monolayers and 3D spheroids. Cells grown in 3D spheroids showed higher proliferation ability and stronger cell-cell adhesion. Spheroids derived from various types of cancer cell lines exhibited distinct morphologies through a geometrical confinement stimulated biomechanical transduction. Z-projected images of cancer cell aggregates were used to analyze 3D multicellular architecture features. Notably, by using a support vector machine classifier, we distinguished tumor cells from normal cells with an accuracy greater than 95%, according to the geometrical features of multicellular spheroids in phase contrast microscopy images. Cancer cells in multicellular spheroid arrays exhibited higher drug resistance of anticancer drug cisplatin than cells grown in 2D cultures. Finally, we developed a co-culture system composed of tumor spheroid arrays, fibroblast cells and photo-crosslinkable gelatin methacryloyl hydrogel to mimic tumor microenvironment which consisted of solid tumor massed, surrounding stromal cells and extracellular matrix. Together, our newly developed simultaneous 2D and 3D cell culture array has great potential in comprehensive evaluation of cellular events in both 2D and 3D, rapid production of spheroid arrays and multicellular geometry-based tumor cell detection.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据