A scalable coaxial bioprinting technology for mesenchymal stem cell microfiber fabrication and high extracellular vesicle yield

2021 ◽  
Author(s):  
Jianwei Chen ◽  
Duchao Zhou ◽  
Zhenguo Nie ◽  
Liang Lu ◽  
Zhidong Lin ◽  
...  

Abstract 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 (~3x10^8 total 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.

2020 ◽  
Vol 62 ◽  
pp. 101106 ◽  
Author(s):  
Abolfazl Rahmani ◽  
Kiarash Saleki ◽  
Nima Javanmehr ◽  
Javad Khodaparast ◽  
Payam Saadat ◽  
...  

Biomaterials ◽  
2020 ◽  
Vol 255 ◽  
pp. 120168 ◽  
Author(s):  
Ning Zhang ◽  
Yanan Song ◽  
Zheyong Huang ◽  
Jing Chen ◽  
Haipeng Tan ◽  
...  

2013 ◽  
Vol 1 (8) ◽  
pp. 860 ◽  
Author(s):  
Ryan S. Stowers ◽  
Charles T. Drinnan ◽  
Eunna Chung ◽  
Laura J. Suggs

Stem Cells ◽  
2017 ◽  
Vol 35 (4) ◽  
pp. 1093-1105 ◽  
Author(s):  
Enrico Ragni ◽  
Federica Banfi ◽  
Mario Barilani ◽  
Alessandro Cherubini ◽  
Valentina Parazzi ◽  
...  

2020 ◽  
Vol 21 (21) ◽  
pp. 7885 ◽  
Author(s):  
Pasquale Simeone ◽  
Christian Celia ◽  
Giuseppina Bologna ◽  
Eva Ercolino ◽  
Laura Pierdomenico ◽  
...  

Extracellular vesicles (EVs) play a crucial role in the intercellular crosstalk. Mesenchymal stem cell-derived EVs (MSC-EVs), displaying promising therapeutic roles, contribute to the strong rationale for developing EVs as an alternative therapeutic option. EV analysis still represents one of the major issues to be solved in order to translate the use of MSC-EV detection in clinical settings. Even if flow cytometry (FC) has been largely applied for EV studies, the lack of consensus on protocols for FC detection of EVs generated controversy. Standard FC procedures, based on scatter measurements, only allows the detection of the “tip of the iceberg” of all EVs. We applied an alternative FC approach based on the use of a trigger threshold on a fluorescence channel. The EV numbers obtained by the application of the fluorescence triggering resulted significantly higher in respect to them obtained from the same samples acquired by placing the threshold on the side scatter (SSC) channel. The analysis of EV concentrations carried out by three different standardized flow cytometers allowed us to achieve a high level of reproducibility (CV < 20%). By applying the here-reported method highly reproducible results in terms of EV analysis and concentration measurements were obtained.


Sign in / Sign up

Export Citation Format

Share Document