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Scientists devise new way to generate canine stem cells
The iPSCs were generated without feeder cells, a process which had not been possible before.
The method reprograms the cells from urine samples.

Researchers have discovered a method to generate canine induced pluripotent stem cells (iPSCs) from urine samples.

The findings could bring companion animal medicine research a step closer to veterinary regenerative treatment.

The research, conducted by scientists at Osaka Metropolitan University, aimed to discover how iPSCs could be used in the study of veterinary regenerative medicine, as well as contributing to new discoveries in human regenerative medicine.

However, canine somatic cells have a much lower reprogramming efficiency than those of humans. This means that there are fewer types of canine cells which can be used to generate iPSCs.

The induction of iPSCs would often use feeder cells from a different species, although it is considered safer to minimise the use of xenogeneic components. Therefore, scientists were keen to find a method of reprogramming various canine cells in dogs without using feeder cells.

The research team were able to identify six reprogramming genes, which could increase canine iPSC generation by 120 times compared to conventional methods using fibroblasts.

Using these genes, the scientists were able to create iPSCs by reprogramming stem cells from canine urine samples. This was a non-invasive, painless and straight-forward method.

Not only were the scientists able to create the cells with reduced xenogeneic components, the iPSCs were also generated without feeder cells, a process which had not been possible before.

It is believed that this discovery could not only further studies of veterinary regenerative medicines, but also lead to new discoveries in human regenerative medicines.

Prof Shingo Hatoya, from the Graduate School of Veterinary Science at Osaka Metropolitan University, led the research team. They said: "As a veterinarian, I have examined and treated many animals,

"However, there are still many diseases that either cannot be cured or have not been fully understood. In the future, I am committed to continue my research on differentiating canine iPSCs into various types of cells and applying them to treat sick dogs, hopefully bringing joy to many animals and their owners."

The full study can be found in the journal Stem Cell Reports.

Image © Shutterstock

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Equine Disease Surveillance report released for Q4 2025

News Story 1
 The latest Equine Disease Surveillance report has been released, with details on equine disease from Q4 of 2025.

The report, produced by Equine Infectious Disease Surveillance, includes advice on rule changes for equine influenza vaccination.

Statistics and maps detail recent outbreaks of equine herpes virus, equine influenza, equine strangles and equine grass sickness. A series of laboratory reports provides data on virology, bacteriology, parasitology and toxicosis.

This issue also features a case study of orthoflavivus-associated neurological disease in a horse in the UK. 

Click here for more...
News Shorts
NSA webinar explores sheep tailing and castration

The National Sheep Association (NSA) is to host a free webinar on the castration and tail docking of lambs.

The webinar, 'Understanding the tailing and castration consultation: A guide for sheep farmers', will be hosted online on Monday, 2 March 2026 at 7.30pm.

It comes during a government consultation into the methods used for these procedures. Farmers are encouraged to engage before the consultation period closes on Monday, 9 March 2026.

The webinar offers clear and actionable guidance to support farmers to contribute meaningfully to the consultation and prepare for potential changes.

On the panel will be former SVS president Kate Hovers, farmer and vet Ann Van Eetvelt and SRUC professor in Animal Health and Veterinary Sciences Cathy Dwyer. Each panel member will utilise their own specialism and expertise to evaluate risks and outcomes to sheep farming.

Find out more about the webinar on the NSA website.