On-Chip Fabrication, Manipulation and Self-Assembly for Three-Dimensional Cell Structures

Author(s):  
Toshio Fukuda ◽  
Tao Yue ◽  
Masaru Takeuchi ◽  
Masahiro Nakajima
2021 ◽  
Author(s):  
Stephan Förster ◽  
Jürgen Groll ◽  
Benjamin Reineke ◽  
Stephan Hauschild ◽  
Ilona Paulus ◽  
...  

Bioprinting has evolved into a thriving technology for the fabrication of cell-laden scaffolds. Bioinks are the most critical component for bioprinting. Recently, microgels have been introduced as a very promising bioink enabling cell protection and the control of the cellular microenvironment. However, their microfluidic fabrication inherently seemed to be a limitation. Here we introduce a direct coupling of microfluidics and 3D-printing for the microfluidic production of cell-laden microgels with direct in-flow bioprinting into stable scaffolds. The methodology enables the continuous on-chip encapsulation of cells into monodisperse microdroplets with subsequent in-flow cross-linking to produce cell-laden microgels, which after exiting a microtubing are automatically jammed into thin continuous microgel filaments. The integration into a 3D printhead allows direct in-flow printing of the filaments into free-standing three-dimensional scaffolds. The method is demonstrated for different cross-linking methods and cell lines. With this advancement, microfluidics is no longer a bottleneck for biofabrication. <br>


2011 ◽  
Vol 2011.19 (0) ◽  
pp. 197-198
Author(s):  
Eijiro Yanai ◽  
Yuichi Isobe ◽  
Hroo Akiyama ◽  
shinjiro Umezu ◽  
Atusi Maruyama ◽  
...  

2021 ◽  
Author(s):  
Stephan Förster ◽  
Jürgen Groll ◽  
Benjamin Reineke ◽  
Stephan Hauschild ◽  
Ilona Paulus ◽  
...  

Bioprinting has evolved into a thriving technology for the fabrication of cell-laden scaffolds. Bioinks are the most critical component for bioprinting. Recently, microgels have been introduced as a very promising bioink enabling cell protection and the control of the cellular microenvironment. However, their microfluidic fabrication inherently seemed to be a limitation. Here we introduce a direct coupling of microfluidics and 3D-printing for the microfluidic production of cell-laden microgels with direct in-flow bioprinting into stable scaffolds. The methodology enables the continuous on-chip encapsulation of cells into monodisperse microdroplets with subsequent in-flow cross-linking to produce cell-laden microgels, which after exiting a microtubing are automatically jammed into thin continuous microgel filaments. The integration into a 3D printhead allows direct in-flow printing of the filaments into free-standing three-dimensional scaffolds. The method is demonstrated for different cross-linking methods and cell lines. With this advancement, microfluidics is no longer a bottleneck for biofabrication. <br>


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.


2020 ◽  
Vol 7 (3) ◽  
pp. 115
Author(s):  
Patrick Bédard ◽  
Sara Gauvin ◽  
Karel Ferland ◽  
Christophe Caneparo ◽  
Ève Pellerin ◽  
...  

Animal testing has long been used in science to study complex biological phenomena that cannot be investigated using two-dimensional cell cultures in plastic dishes. With time, it appeared that more differences could exist between animal models and even more when translated to human patients. Innovative models became essential to develop more accurate knowledge. Tissue engineering provides some of those models, but it mostly relies on the use of prefabricated scaffolds on which cells are seeded. The self-assembly protocol has recently produced organ-specific human-derived three-dimensional models without the need for exogenous material. This strategy will help to achieve the 3R principles.


2014 ◽  
Vol 2 (20) ◽  
pp. 3123-3132 ◽  
Author(s):  
Ming-Hao Yao ◽  
Jie Yang ◽  
Ming-Shuo Du ◽  
Ji-Tao Song ◽  
Yong Yu ◽  
...  

A class of physical hydrogels photo-cross-linked from multi-branched photopolymeriized monomers based on the self-assembly of coiled-coil polypeptide P is developed.


2015 ◽  
Vol 9 (3) ◽  
pp. 034113 ◽  
Author(s):  
Mi Jang ◽  
Pavel Neuzil ◽  
Thomas Volk ◽  
Andreas Manz ◽  
Astrid Kleber

2006 ◽  
Vol 18 (5) ◽  
pp. 611-614 ◽  
Author(s):  
V. Jayawarna ◽  
M. Ali ◽  
T. A. Jowitt ◽  
A. F. Miller ◽  
A. Saiani ◽  
...  

2020 ◽  
Vol 11 (1) ◽  
pp. 18 ◽  
Author(s):  
Masaru Takeuchi ◽  
Taro Kozuka ◽  
Eunhye Kim ◽  
Akihiko Ichikawa ◽  
Yasuhisa Hasegawa ◽  
...  

We developed a procedure for fabricating movable biological cell structures using biodegradable materials on a microfluidic chip. A photo-cross-linkable biodegradable hydrogel gelatin methacrylate (GelMA) was used to fabricate arbitrary microstructure shapes under a microscope using patterned ultraviolet light. The GelMA microstructures were movable inside the microfluidic channel after applying a hydrophobic coating material. The fabricated microstructures were self-assembled inside the microfluidic chip using our method of fluid forcing. The synthesis procedure of GelMA was optimized by changing the dialysis temperature, which kept the GelMA at a suitable pH for cell culture. RLC-18 rat liver cells (Riken BioResource Research Center, Tsukuba, Japan) were cultured inside the GelMA and on the GelMA microstructures to check cell growth. The cells were then stretched for 1 day in the cell culture and grew well on the GelMA microstructures. However, they did not grow well inside the GelMA microstructures. The GelMA microstructures were partially dissolved after 4 days of cell culture because of their biodegradability after the cells were placed on the microstructures. The results indicated that the proposed procedure used to fabricate cell structures using GelMA can be used as a building block to assemble three-dimensional tissue-like cell structures in vitro inside microfluidic devices.


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