Completed Cells, Biochemistry & Physiology Heart, Stroke & Blood

Probing the mechanical control of stem cell fate through the development of novel, non-invasive imaging technologies

In plain English

AI plain-English summary

Stem cells tagged with molecular labels can now be tracked inside living tissue without destroying the cells or harming the patient. This matters because stem cells behave differently in the lab than inside the body. Researchers cannot currently follow where individual stem cells go, how many times they divide, or what they turn into once implanted. Without that knowledge, doctors cannot reliably direct stem cells to repair a specific damaged tissue—a bone defect, a torn cartilage, or a failing organ. The project brings together physicists, engineers, and biologists to build new microscopes that see deep into tissue and new molecular markers that do not interfere with cell function. If the work succeeds, it will give surgeons a way to watch stem cells in real time after transplantation. They could then adjust the mechanical stiffness or structure of the surrounding tissue to steer the cells toward the desired cell type—bone, muscle, or nerve. The ultimate goal is to grow custom tissues on demand, either in the lab or directly inside a patient, turning stem cell therapy from a laboratory curiosity into a reliable clinical tool.

View original technical description
Whilst in our increasing ageing population stem cell science and technology holds a great deal of promise within the context of tissue repair and regeneration, moving this technology to the clinics has been relatively slow due to a number of distinct 'barriers'. For example, whilst we know a lot about the function and response of stem cells in the laboratory, we know very little about their behaviour in tissues within individuals. A further major barrier has been the inability to accurately track cell lineages and to distinguish them from other cell types within the tissue (i.e. when one cell divides to become two cells are they the same or different? Is this effect the same or different each time the cell divides? Where do they go?). This application will address these issues by bringing together researchers across different scientific disciplines in the physical and life sciences to develop novel technologies for stem cell science. Specifically, we will develop new ways of non-destructively labelling stem cells by manipulating molecules within the cells so we can follow both their position and their eventual fate (i.e. what do these stem cells turn into?). In order to image the cells we will develop new microscopic techniques that allow us to view these cells in a non-invasive, non-harmful way (unlike current approaches) and we will utilise technologies that will eventually enable us to image these cells deep within patient tissues. Being able to follow these stem cells will allow us to examine the mechanical influence of their surrounding tissue environments. Armed with such knowledge we will mechanically manipulate the surrounding environment to direct stem cells into our tissue of choice in order to deliver custom designed tissues on demand (either within the laboratory or eventually within a patient). Overall, our ultimate aim is to develop new tools to allow us to investigate and control stem cell biology in order to realise the true clinical potential of these cells.

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Researchers

Alastair Sloan (Co-Investigator)C Wright (Co-Investigator)Eric Michael Tippmann (Co-Investigator)Karl Hawkins (Co-Investigator)Paola Borri (Co-Investigator)Phil Stephens (Principal Investigator)Rachel Errington (Co-Investigator)Rhodri Williams (Co-Investigator)Stephen Paisey (Co-Investigator)Susan MacLean Hunter (Co-Investigator)Wolfgang Langbein (Co-Investigator)

Related Research

Grants with similar aims, by meaning.

Automatic cell fate engineering using microfluidics devices
The development and application of non-invasive imaging technologies for investigating the behaviour of administered stem cells
Single cell live imaging in vivo, to understand cell activity in the context of regenerative medicine and cancer biology.
The use of microRNAs and nanotopography to modulate skeletal stem cell fate and function
Looking into the Crystal Ball: Uncovering Predictive Mechanical Cues for Cell Choices in Development and Disease'

Original classification

Research Grant

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