Reversible physical crosslinking strategy with optimal temperature for 3D bioprinting of human chondrocyte-laden gelatin methacryloyl bioink

2018 ◽  
Vol 33 (5) ◽  
pp. 609-618 ◽  
Author(s):  
Yawei Gu ◽  
Lei Zhang ◽  
Xiaoyu Du ◽  
Ziwen Fan ◽  
Long Wang ◽  
...  

Gelatin methacryloyl is a promising material in tissue engineering and has been widely studied in three-dimensional bioprinting. Although gelatin methacryloyl possesses excellent biocompatibility and tunable mechanical properties, its poor printability/processability has hindered its further applications. In this study, we report a reversible physical crosslinking strategy for precise deposition of human chondrocyte-laden gelatin methacryloyl bioink at low concentration without any sacrificial material by using extrusive three-dimensional bioprinting. The precise printing temperature was determined by the rheological properties of gelatin methacryloyl with temperature. Ten percent (w/v) gelatin methacryloyl was chosen as the printing formula due to highest biocompatibility in three-dimensional cell cultures in gelatin methacryloyl hydrogel disks. Primary human chondrocyte-laden 10% (w/v) gelatin methacryloyl was successfully printed without any construct deformation or collapse and was permanently crosslinked by ultraviolet light. The printed gelatin methacryloyl hydrogel constructs remained stable in long-term culture. Chondrocyte viability and proliferation that were printed under this optimal temperature were better than that of chondrocytes printed under lower temperatures and were similar to that of chondrocytes in the non-printed gelatin methacryloyl hydrogels. The results indicate that with this strategy, 10% (w/v) gelatin methacryloyl bioink presented excellent printability and printing resolution with high cell viability, which appears to be suitable for printing primary human chondrocytes in cartilage biofabrication and can be extensively applied in tissue engineering of other organs or in other biomedical fields.

2012 ◽  
Vol 18 (7) ◽  
pp. 496-506 ◽  
Author(s):  
Shawn P. Grogan ◽  
Chantal Pauli ◽  
Peter Chen ◽  
Jiang Du ◽  
Christine B. Chung ◽  
...  

2014 ◽  
Vol 115 (17) ◽  
pp. 172616 ◽  
Author(s):  
Ruogang Zhao ◽  
Thomas Boudou ◽  
Wei-Gang Wang ◽  
Christopher S. Chen ◽  
Daniel H. Reich

2014 ◽  
Vol 6 (10) ◽  
pp. 988-998 ◽  
Author(s):  
Francesco Pampaloni ◽  
Ulrich Berge ◽  
Anastasios Marmaras ◽  
Peter Horvath ◽  
Ruth Kroschewski ◽  
...  

This novel system for the long-term fluorescence imaging of live three-dimensional cultures provides minimal photodamage, control of temperature, CO2, pH, and media flow.


Lab on a Chip ◽  
2015 ◽  
Vol 15 (3) ◽  
pp. 920-930 ◽  
Author(s):  
H. K. Chu ◽  
Z. Huan ◽  
J. K. Mills ◽  
J. Yang ◽  
D. Sun

A multi-layer scaffold incorporating dielectrophoresis for automated cell manipulation is developed to construct 3D cellular patterns for tissue engineering applications.


2021 ◽  
Author(s):  
Clément Quintard ◽  
Gustav Jonsson ◽  
Camille Laporte ◽  
Caroline Bissardon ◽  
Amandine Pitaval ◽  
...  

The development of vascular networks on-chip is crucial for the long-term culture of three-dimensional cell aggregates such as organoids, spheroids, tumoroids, and tissue explants. Despite the rapid advancement of microvascular network systems and organoid technology, vascularizing organoids-on-chips remains a challenge in tissue engineering. Moreover, most existing microfluidic devices poorly reflect the complexity of in vivo flows and require complex technical settings to operate. Considering these constraints, we developed an innovative platform to establish and monitor the formation of endothelial networks around model spheroids of mesenchymal and endothelial cells as well as blood vessel organoids generated from pluripotent stem cells, cultured for up to 15 days on-chip. Importantly, these networks were functional, demonstrating intravascular perfusion within the spheroids or vascular organoids connected to neighbouring endothelial beds. This microphysiological system thus represents a viable organ-on-chip model to vascularize biological tissues and should allow to establish perfusion into organoids using advanced microfluidics.


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