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PETBioNewsNewsHuman stem cells reverse multiple sclerosis in mice

BioNews

Human stem cells reverse multiple sclerosis in mice

Published 16 May 2014 posted in News and appears in BioNews 754

Author

Alice Plein

Image by K Hardy via the Wellcome Collection. Depicts a human embryo at the blastocyst stage (about six days after fertilisation) 'hatching' out of the zona pellucida.
CC BY 4.0
Image by K Hardy via the Wellcome Collection. Depicts a human embryo at the blastocyst stage (about six days after fertilisation) 'hatching' out of the zona pellucida.

Mice with a viral form of multiple sclerosis are able to walk again after receiving a transplant of human stem cells, scientists report...

Mice
with a viral form of multiple sclerosis (MS) are able to walk again after receiving
a transplant of human stem cells, scientists report.

Researchers
had injected neural stem cells into the spinal cord of the mice expecting them
to be rejected, but instead they witnessed a surprising recovery.

Professor Tom
Lane
from the University of Utah,
who led the research group, said: 'My postdoctoral fellow Dr Lu Chen came to me
and said, "The mice are walking". I didn’t believe her'.

The study opens up a new
research area for patients with MS, which affects 2.3 million people worldwide.
In MS, the body’s immune system targets myelin, the fatty insulation
surrounding nerve fibres. This leads to impaired nerve signal transmission,
causing widespread symptoms such as loss of vision and motor skills, fatigue, and
slurred speech. At present, drugs that dampen the immune system can slow down
the early stages of the disease but there is no treatment for patients at the latter
stages of MS.

The
scientists transformed human embryonic stem cells into neural precursor cells, which
have the potential to develop into all the types of cell in the nervous system.
Once injected into the mice, they released chemicals that eased the
symptoms of MS. This was a result of an unusually low number of neural
precursor cells being grown within each lab dish, which meant that more
beneficial proteins were released after transplantation.

The
exact nature of these proteins remains to be discovered, but the researchers
believe that they hold the potential for future treatments.

Professor
Lane explained 'Rather than having to engraft stem cells into a patient, which
can be challenging from a medical standpoint, we might be able to develop a
drug that can be used to deliver the therapy much more easily'.

Dr
Sorrel Bickley, from the MS Society, commented: 'This is an
interesting, early-stage study that's given scientists new ideas for future
research into potential MS therapies. It's not currently being planned for
testing in people, but it's a useful avenue for scientists to explore — we look
forward to seeing how this area of research develops'.

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