A scalable coaxial bioprinting technology for mesenchymal stem cell microfiber fabrication and high extracellular vesicle yield.
Jianwei ChenDuchao ZhouZhenguo NieLiang LuZhidong LinDezhi ZhouYi ZhangXiaoyan LongSiyang FanTao XuPublished in: Biofabrication (2021)
Mesenchymal stem cell (MSC)-derived extracellular vesicles (EVs) are promising candidates for regenerative medicine; however, the lack of scalable methods for high quantity EV production limits their application. In addition, signature EV-derived proteins shared in 3D environments and 2D surfaces, remain mostly unknown. Herein, we present a platform combining MSC microfiber culture with ultracentrifugation purification for high EV yield. Within this platform, a high quantity MSC solution (∼3 × 108total cells) is encapsulated in a meter-long hollow hydrogel-microfiber via coaxial bioprinting technology. In this 3D core-shell microfiber environment, MSCs express higher levels of stemness markers (Oct4, Nanog, Sox2) than in 2D culture, and maintain their differentiation capacity. Moreover, this platform enriches particles by ∼1009-fold compared to conventional 2D culture, while preserving their pro-angiogenic properties. Liquid chromatography-mass spectrometry characterization results demonstrate that EVs derived from our platform and conventional 2D culturing have unique protein profiles with 3D-EVs having a greater variety of proteins (1023 vs 605), however, they also share certain proteins (536) and signature MSC-EV proteins (10). This platform, therefore, provides a new tool for EV production using microfibers in one culture dish, thereby reducing space, labor, time, and cost.
Keyphrases
- mass spectrometry
- mesenchymal stem cells
- high throughput
- liquid chromatography
- stem cells
- umbilical cord
- drug delivery
- staphylococcus aureus
- escherichia coli
- cystic fibrosis
- high resolution mass spectrometry
- high resolution
- optical coherence tomography
- oxidative stress
- pseudomonas aeruginosa
- tissue engineering
- cancer stem cells
- cell proliferation
- single cell
- cell death
- biofilm formation
- amino acid
- recombinant human