scholarly journals Small-Scale Fluidized Bed Bioreactor for Long-Term Dynamic Culture of 3D Cell Constructs and in vitro Testing

Author(s):  
Joana Mendonça da Silva ◽  
Eloy Erro ◽  
Maooz Awan ◽  
Sherri-Ann Chalmers ◽  
Barry Fuller ◽  
...  
2010 ◽  
Vol 11 (3) ◽  
pp. 657-665 ◽  
Author(s):  
Rodrigo Oréfice ◽  
Jon West ◽  
Guy LaTorre ◽  
Larry Hench ◽  
Anthony Brennan

2015 ◽  
Vol 39 (10) ◽  
pp. 897-902 ◽  
Author(s):  
Lukas Kneisz ◽  
Ewald Unger ◽  
Hermann Lanmüller ◽  
Winfried Mayr

2005 ◽  
Vol 19 (7) ◽  
pp. 845-852 ◽  
Author(s):  
Helga Tuschl ◽  
Christina E. Schwab

2015 ◽  
Vol 39 (11) ◽  
pp. 973-978 ◽  
Author(s):  
Giulia Mazza ◽  
Martin Stoiber ◽  
Dagmar Pfeiffer ◽  
Heinrich Schima

2021 ◽  
Author(s):  
Sergei Grebeniuk ◽  
Abdel Rahman Abdel Fattah ◽  
Gregorius Rustandi ◽  
Manoj Kumar ◽  
Burak Toprakhisar ◽  
...  

The vascularization of engineered tissues and organoids has remained a major unresolved challenge in regenerative medicine. While multiple approaches have been developed to vascularize in vitro tissues, it has thus far not been possible to generate sufficiently dense networks of small-scale vessels to perfuse large de novo tissues. Here, we achieve the perfusion of multi-mm3 tissue constructs by generating networks of synthetic capillary-scale 3D vessels. Our 3D soft microfluidic strategy is uniquely enabled by a 3D-printable 2-photon-polymerizable hydrogel formulation, which allows for precise microvessel printing at scales below the diffusion limit of living tissues. We demonstrate that these large-scale engineered tissues are viable, proliferative and exhibit complex morphogenesis during long-term in-vitro culture, while avoiding hypoxia and necrosis. We show by scRNAseq and immunohistochemistry that neural differentiation is significantly accelerated in perfused neural constructs. Additionally, we illustrate the versatility of this platform by demonstrating long-term perfusion of developing liver tissue. This fully synthetic vascularization platform opens the door to the generation of human tissue models at unprecedented scale and complexity.


2006 ◽  
Vol 39 ◽  
pp. S50 ◽  
Author(s):  
G. von Skrbensky ◽  
R. Huber
Keyword(s):  

2006 ◽  
Vol 94 (5) ◽  
pp. 949-960 ◽  
Author(s):  
Claudio Garibay-Orijel ◽  
Carlos Hoyo-Vadillo ◽  
Teresa Ponce-Noyola ◽  
Jaime García-Mena ◽  
Héctor Mario Poggi-Varaldo

2010 ◽  
Vol 38 (5) ◽  
pp. 1919-1927 ◽  
Author(s):  
Martina Schleicher ◽  
Günther Sammler ◽  
Michael Schmauder ◽  
Olaf Fritze ◽  
Agnes J. Huber ◽  
...  

2021 ◽  
Author(s):  
Sergei Grebenyuk ◽  
Abdel Rahman Abdel Fattah ◽  
Gregorius Rustandi ◽  
Manoj Kumar ◽  
Burak Toprakhisar ◽  
...  

Abstract The vascularization of engineered tissues and organoids has remained a major unresolved challenge in regenerative medicine. While multiple approaches have been developed to vascularize in vitro tissues, it has thus far not been possible to generate sufficiently dense networks of small-scale vessels to perfuse large de novo tissues. Here, we achieve the perfusion of multi-mm3 tissue constructs by generating networks of synthetic capillary-scale 3D vessels. Our 3D soft microfluidic strategy is uniquely enabled by a 3D-printable 2-photon-polymerizable hydrogel formulation, which allows for precise microvessel printing at scales below the diffusion limit of living tissues. We demonstrate that these large-scale engineered tissues are viable, proliferative and exhibit complex morphogenesis during long-term in-vitro culture, while avoiding hypoxia and necrosis. We show by scRNAseq and immunohistochemistry that neural differentiation is significantly accelerated in perfused neural constructs. Additionally, we illustrate the versatility of this platform by demonstrating long-term perfusion of developing liver tissue. This fully synthetic vascularization platform opens the door to the generation of human tissue models at unprecedented scale and complexity.


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