Researchers at University
of Galway have developed a way of bioprinting tissues that change shape as a
result of cell-generated forces, in the same way that it happens in biological
tissues during organ development.
The breakthrough science focused on
replicating heart tissues, bringing research closer to generating functional,
bioprinted organs, which would have broad applications in disease modelling,
drug screening and regenerative medicine.
The research was led by a team at the
School of Engineering and CÚRAM Research Ireland Centre for Medical Devices at
University of Galway and has been published in the journal Advanced
Functional Materials.
Bioprinting technology uses living cells
within specialised “bioink” materials – a substance or material which can
support living cells, and due to its characteristics, it can aid cell adhesion,
proliferation and differentiation during maturation. The technology offers
immense promise for creating lab-grown organs that closely resemble the
structure of their human equivalent.
However, bioprinting fully functional
organs remains a significant hurdle. For instance, while bioprinted heart
tissues can contract, their force of contraction is often considerably weaker
than that of a healthy adult heart.
Traditional bioprinting methods often
aim to directly recreate the final anatomical shape of an organ, like the heart
– therefore overlooking the crucial role of dynamic shape changes during
natural embryonic development. For example, the heart begins as a simple tube
that undergoes a series of bends and twists to form its mature four-chambered
structure. These shape-morphing behaviours are essential for sculpting heart
cell development and maturation.
The University of Galway research team
recognised this and developed a novel bioprinting technique that incorporates
crucial shape-changing behaviours.
Ankita
Pramanick, lead author of the study and CÚRAM PhD Candidate at University of
Galway, said: “Our work
introduces a novel platform, using embedded bioprinting to bioprint tissues
that undergo programmable and predictable 4D shape-morphing driven by
cell-generated forces. Using this new process, we found that shape-morphing
improved the structural and functional maturity of bioprinted heart tissues.”
The research showed that cell-generated
forces could guide the shape-morphing of bioprinted tissues, and it was
possible to control the magnitude of the shape changes by modifying factors
such as the initial print geometry and bioink stiffness. Morphing was found to
sculpt cell alignment and enhance the contractile properties of the tissues.
The research team also developed a computational model that could predict
tissue shape-morphing behaviour.
Professor
Andrew Daly, Associate Professor in Biomedical Engineering and CÚRAM funded
investigator and principal investigator on the project, said: “Our research shows that by allowing bioprinted
heart tissues to undergo shape-morphing, they start to beat stronger and
faster. The limited maturity of bioprinted tissues has been a major challenge
in the field, so this was an exciting result for us. This allows us to create
more advanced bioprinted heart tissue, with the ability to mature in a
laboratory setting, better replicating adult human heart structure. We are
excited to build on this shape-morphing approach in our ongoing European
Research Council project, which is focused on developmentally-inspired
bioprinting.
“We are still a long way away from
bioprinting functional tissue that could be implanted in humans, and future
work will need to explore how we can scale our bioprinting approach to
human-scale hearts.
“We will need to integrate blood vessels
to keep such large constructs alive in the lab, but ultimately, this
breakthrough brings us closer to generating functional bioprinted organs, which
would have broad applications in cardiovascular medicine.”
Journal article: https://advanced.onlinelibrary.wiley.com/doi/10.1002/adfm.202414559
Source: Researchers make breakthrough in bioprinting functional human heart tissue – Scents of Science
No comments:
Post a Comment