A microfluidic hanging drop-based spheroid co-culture platform for probing tumor angiogenesis.
Didem RodopluJefunnie Sierra MatahumChia-Hsien HsuPublished in: Lab on a chip (2022)
Co-culturing of embryoid bodies (EBs) and tumor spheroids (TSs) allows mimicking tumor angiogenesis in vitro . Here, we report a microfluidic hanging drop-based spheroid co-culture device (μ-CCD) that permits the generation and co-culturing of EBs and TSs using a simple manual operation procedure and setup. In brief, uniform-sized EBs and TSs can be generated on the device in eight pairs of hanging droplets from adjacent microfluidic channels, followed by the confrontation of EB and TS pairs by merging the droplet pairs to culture the EB-TS spheroids to investigate tumor-induced angiogenic sprouting. The physical parameters of the device were optimized to maintain the long-term stability of hanging droplets for up to ten days. The mouse embryonic stem cell line ES-D3 and breast cancer cell lines MDA-MB-231 and MCF-7 were used to generate EBs, invasive TSs, and non-invasive TSs respectively. Confocal imaging results showed that the vessel percentage area and total vessel length which are linked to tumor angiogenesis increased after 6 days of co-culturing. An anti-angiogenesis drug testing on the co-cultured EB-TS spheroids was also demonstrated in the device. The μ-CCD provides a simple yet high-efficiency method to generate and co-culture cell spheroids and may also be useful for other applications involving spheroid co-culturing.
Keyphrases
- endothelial cells
- single cell
- high throughput
- high efficiency
- vascular endothelial growth factor
- mental health
- high resolution
- oxidative stress
- wound healing
- mesenchymal stem cells
- emergency department
- signaling pathway
- molecular dynamics simulations
- diabetic rats
- minimally invasive
- cell death
- bone marrow
- optical coherence tomography
- electronic health record