Need different types of tissue? Just print them.

What sounds like a dream of the future has already been the subject of research for a few years: simply printing out tissue and organs. Scientists have refined the technology and now are producing a variety of tissue types.

One technology might assume a decisive role in this effort – one that we are all familiar with from the office, and that most of us would certainly not immediately connect with the production of artificial tissue: the inkjet printer. Scientists of the Fraunhofer Institute for Interfacial Engineering and Biotechnology (IGB) in Stuttgart, Germany, have succeeded in developing suitable bio-inks for this printing technology. The transparent liquids consist of components from the natural tissue matrix and living cells. The substance is based on a well-known biological material, gelatin, which is derived from collagen, the main constituent of native tissue. The researchers have chemically modified the gelling behavior of the gelatin to adapt the biological molecules for printing. Instead of gelling like unmodified gelatin, the bio-inks remain fluid during printing. Only after they are irradiated with UV light, they crosslink and cure to form hydrogels. These are polymers containing a huge amount of water (just like native tissue), but which are stable in aqueous environments and when being warmed to physiological 37°C. The researchers can control the chemical modification of the biological molecules so that the resulting gels have differing strengths and swelling characteristics. The properties of natural tissue can therefore be imitated – from solid cartilage to soft adipose tissue.

In Stuttgart, synthetic raw materials also are printed that can serve as substitutes for the extracellular matrix. For example, a system that cures to a hydrogel devoid of by-products and can be immediately populated with genuine cells.

“We are concentrating at the moment on the natural variant. That way we remain very close to the original material. Even if the potential for synthetic hydrogels is big, we still need to learn a fair amount about the interactions between the artificial substances and cells or natural tissue. Our biomolecule-based variants provide the cells with a natural environment instead, and therefore can promote the self-organizing behavior of the printed cells to form a functional tissue model,” explains Dr. Kirsten Borchers, a researcher at Fraunhofer IGB.

The printers at the labs in Stuttgart have a lot in common with conventional office printers: The ink reservoirs and jets are all the same. The differences are discovered only under close inspection. For example, there is a heater on the ink container with which the right temperature of the bio-inks is set and the number of jets and tanks is smaller than in the office counterpart.

“We would like to increase the number of these in cooperation with industry and other Fraunhofer Institutes in order to simultaneously print using various inks with different cells and matrices. This way we can come closer to replicating complex structures and different types of tissue,” Borchers says.

The big challenge now is to produce vascularized tissue that has its own system of blood vessels through which the tissue can be provided with nutrients. IGB is working on this jointly with other partners under Project ArtiVasc 3D, supported by the European Union. The core of this project is a technology platform to generate fine blood vessels from synthetic materials and thereby create for the first time artificial skin with its subcutaneous adipose tissue.

“This step is very important for printing tissue or entire organs in the future. Only once we are successful in producing tissue that can be nourished through a system of blood vessels can printing larger tissue structures become feasible,” Borchers concludes.

Adapted from an original release from Fraunhofer Institute for Interfacial Engineering and Biotechnology (IGB), www.fraunhofer.de/en.html.

Elizabeth Engler Modic is the editor of TMD and can be contacted at emodic@gie.net or 330.523.5344.