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September 13, 2023

Novel microvessel printing enables 3D perfusion of large tissues

perfused tissue covered the entire volume of the 3D-printed microvascular grid
Over time, the perfused tissue covered the entire volume of the 3D-printed microvascular grid in a uniformly dense manner. At the periphery, bulging epithelial outgrowths characteristic of cerebral organoids are observed, indicating a higher cell proliferation in the perfused grids, compared to the non-perfused samples. Image: See source below this article.

A major challenge in regenerative medicine is the vascularization of engineered tissues to create dense networks of microscale vessels that can perfuse even large volumes of tissues. A new microfluidic strategy, enabled by Two-Photon Polymerization-based 3D printing, allows the fabrication of networks of synthetic 3D microvessels, consisting of tubular 3D hydrogel structures. These complex microfluidic systems can perfuse tissues many cubic millimeters in size. This allows the tissues to survive for long periods of time and show cell proliferation and differentiation in the in vitro cultures. The results of this novel synthetic vascularization platform are a crucial starting point for the realization of complex human tissue models.

Artificial human tissues and organoids or “mini-organs” have potential in biology and biomedicine to help understand cell proliferation, tissue dynamics, and disease. They could potentially be used in regenerative medicine and drug discovery studies. By providing unparalleled complexity, large-scale tissue models are expected to mimic the properties of their human in vivo counterparts, offering a very promising alternative to animal testing.
However, microscale vascularization is critical to reproduce the in vivo-like environment in bio-engineered tissues. The presence of a network of microvessels, made up of capillaries, is essential for microcirculation and the exchange of oxygen, nutrients and waste products. Scientists at the KU Leuven have addressed this issue and succeeded in fabricating a 3D soft microfluidic lattice that can perfuse large tissue constructs in the cubic multi-millimeter range. A hydrogel material that is permeable for gases and nutrients was chosen for the fabrication of the soft microfluidic lattices.

3D printing of microvessel networks

Nanoscribe’s Two-Photon Polymerization (2PP) is the key technology that enables the fabrication of a highly interconnected network of synthetic microvessels. The precision capabilities of the 2PP-based 3D printers enabled the fabrication of filigree capillary-like tubes with diameters and thicknesses of a few microns. The printers are also capable to perform this type of fabrication over cubic multi-millimeter volumes. Thus the complex geometry of the vascular network can ensure perfusion over a large three-dimensional space of several tens of cubic millimeters. Importantly, the rapid prototyping capabilities of Nanoscribe’s technology allowed the shape-accurate printing of the CAD geometry, making it the ideal technology for this challenging microfabrication task.

Customized non-swelling hydrogel biomaterial

The clue to the required diffusion characteristics of the vascular network lies in the choice of material. The scientists developed a custom material based on a soft, non-swelling hydrogel that allows the exchange of oxygen, nutrients and waste. The non-swelling properties of the hydrogel are essential to avoid breaking the seal between the soft microfluidic grid and the plastic base on which the grid was 3D printed. The choice of the non-swelling hydrogel is also possible because Nanoscribe’s 3D printers are designed as open material systems that are compatible with the use of customizable, third-party and commercially available materials, extending the flexibility often required in microfabrication.

Accelerated cell differentiation in perfused tissue

The novel 3D soft microfluidic cell culture platform provides microperfusion for various tissue constructs. Starting from stem cells, the scientists produced cerebral organoids and liver tissue constructs using controlled differentiation, a process through which stem cells acquire their specific roles in the body (e.g., become neurons or hepatocytes). They discovered that microperfusion significantly enhanced tissue growth and accelerated differentiation process compared to non-perfused tissues and conventional cell culturing. Furthermore, the analysis of the perfused neural tissue confirmed the high viability of the tissues over long periods of time.

Would you like to find out more about this inspiring project? Then read the open-access publication here: Large-scale perfused tissues via synthetic 3D soft microfluidics

The complete publication and further scientific publications on hundreds of research projects can be found in a powerful database with an underpinned keyword search in the Premium Resources section. Register for free and gain insights into the potential of Nanoscribe’s 3D Microfabrication technology for innovative applications and fundamental innovations in many areas.

Close-up image of the 3D-printed soft microfluidic capillary lattice made of a non-swelling hydrogel material
Close-up image of the 3D-printed soft microfluidic capillary lattice made of a non-swelling hydrogel material. Image: KU Leuven
Immunofluorescence images show evidence of cell death in the inner core of the control organoid and the non-perfused tissue (Csp3, green, middle column) and its absence in the perfused organoid. The samples stained for HIF1α (green, left column), indicate high levels of oxygen starvation in the control and non-perfused organoids.
Immunofluorescence images show evidence of cell death in the inner core of the control organoid and the non-perfused tissue (Csp3, green, middle column) and its absence in the perfused organoid. The samples stained for HIF1α (green, left column), indicate high levels of oxygen starvation in the control and non-perfused organoids. Image: See source below this article.
Bright field images of neural spheroids over the two-month culture period.  The organoid in the perfused grid showed progressive growth, while in the non-perfused grid a malformed fibrous-like tissue was produced
Bright field images of neural spheroids over the two-month culture period. The organoid in the perfused grid showed progressive growth, while in the non-perfused grid a malformed fibrous-like tissue was produced. Image: Source is found below this article.

 

Image source

CC BY 4.0 S. Grebenyuk et al., Nat Commun 14, 193 (2023), KU Leuven.

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