Researchers Print Living Skin With Blood Vessels in 3D

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For the first time, a team of researchers managed to print human skin, including blood vessels, in 3D. This is a dramatic advance that gives hope for future skin grafts that fully integrate into the patient’s skin.

This is a novelty that will make history in the field of 3D bio-printing.

3D Printing
3D Printing

In an article published in the journal Tissue Engineering Part A, scientists at the Rensselaer Polytechnic Institute in the United States explain that they have developed a means to print live and vascularized human skin in 3D. This is an important first step to create grafts that look more like the skin our body naturally produces.

A “biological ink” that is grafted onto human skin

So far, attempts to achieve three-dimensional bio-impression of human tissue have been hampered by the lack of a functional vascular system in the grafts.

“Currently, everything that is available as a clinical product looks more like a luxury dressing,” says Pankaj Karande, who led the work. “It accelerates the healing process, but eventually falls away, never really integrating with the host cells.

So the challenge for the researchers has been to recreate this vascularization in 3D printed grafts. Professor Karande has been working on the subject for many years and has shown in previous work that it is possible to take two types of human cells and transform them into “biotins” to print them on a skin-like structure.

This new research goes further because researchers have added human endothelial cells, which cover the inside of blood vessels, and human pericycle cells, which surround endothelial cells, to this “bio ink”. As a result, the cells began to communicate with each other and form a vascular structure within a few weeks.

There are still no clinical studies in sight

Once the graft was made, scientists grafted it onto a mouse. They then discovered that the imprinted blood vessels began to communicate and connect with the rodent’s. “This is extremely important because we know that there is actually a transfer of blood and nutrients to the graft, which keeps the graft alive,” says Prof. Karande.

Many steps are still needed before this technology can be made clinically usable. In particular, researchers must be able to modify donor cells using CRISPR technology so that the vessels can be integrated and accepted by the patient’s body. “We haven’t gotten that far yet, but we’re a little bit closer now,” said the lead investigator.

If the study authors’ goal is to produce grafts for burn patients with nerve and vascular damage, it will be a long way to go. At the moment, the grafts created could help patients with diabetes or pressure ulcers in particular. “For these patients it would be perfect, because ulcers usually appear in different parts of the body and can be treated with smaller pieces of skin,” says Prof. Karande. “Healing usually takes longer in diabetic patients, and this could also help speed up the process.

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References:

https://www.liebertpub.com/doi/10.1089/ten.tea.2019.0201

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