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May 13, 2025

Scientists increase complexity of tissue models, providing an alternative to using animals in science

Configuration of (a) Chip-S1 (Emulate Inc.), (b) Organoplate3-lane 64 (MIMETAS) and (c) Chip-A1 (Emulate Inc.). See text for detailed description of each configuration. A cross-section of the coculture region for each of the chip formats is shown (not to scale). Credit: Journal of Tissue Engineering (2025). DOI:10.1177/20417314251326256
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Configuration of (a) Chip-S1 (Emulate Inc.), (b) Organoplate3-lane 64 (MIMETAS) and (c) Chip-A1 (Emulate Inc.). See text for detailed description of each configuration. A cross-section of the coculture region for each of the chip formats is shown (not to scale). Credit: Journal of Tissue Engineering (2025). DOI:10.1177/20417314251326256

Bioengineers at Queen Mary University of London have taken a significant step forward in the development of laboratory-based models of human tissues that may be used as alternatives to animal testing.

The group develops organ-on-a- in which are grown in tiny plastic "chips" to mimic the biology of tissues found in the body. In their latest research, in the Journal of Tissue Engineering, the team describes new methods to increase the complexity of these models, making them even more like human tissues.

The study offers a new way to precisely guide cell behavior by controlling the spatial distribution of growth factors, which act as biological signaling molecules. By doing so, the team was able to recreate different tissues in different locations, mimicking the interfaces between tissues which are critical in both health and disease.

"The tissues in our bodies are incredibly complex, and recreating this complexity in the laboratory is difficult, said Dr. Tim Hopkins, the lead researcher in the study. "Techniques such as organ-on-a-chip offer an improved option to generate tissue models but, until now, methods to really mimic tissue complexity in these models were lacking.

"By creating gradients of growth factors, we can recreate the complex environment that cells experience in the body, so that they behave in the same way in our models."

What makes this breakthrough especially exciting is that the new methods work across a range of different human tissues and different commercial platforms. This means that the research can be used to help scientists understand disease processes and test new therapies across a wide range of human diseases, without the use of animals, which often poorly predict human biology.

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"This work could make a big difference to how we study diseases and test drugs," said Professor Martin Knight, Co-Director of Queen Mary's Center for Predictive in vitro Models. "This research could help speed up the development of safer, more effective treatments, and reduce our reliance on ."

To demonstrate the capability of these new methods, Professor Knight, Dr. Hopkins and the team used a called bone morphogenetic protein-2 (BMP-2) which is heavily involved in bone development.

By creating regions in the organ-chips with high and low concentrations of BMP-2, the researchers could control the behavior of human stem cells within the system, generating bone-like regions interfacing with cartilage-like regions, and mimicking the natural process of bone development.

More information: Timothy Hopkins et al, Engineering growth factor gradients to drive spatiotemporal tissue patterning in organ-on-a-chip systems, Journal of Tissue Engineering (2025).

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Advanced organ-on-a-chip models now enable precise spatial control of growth factors, allowing human cells to form complex, tissue-like structures and interfaces. This approach replicates key aspects of human tissue biology, supports disease modeling and drug testing across various tissues, and offers a promising alternative to animal testing.

This summary was automatically generated using LLM.