Hi all,
hope all are doing fine
pasting below article, which get from another list.
Regards
Wahid

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Photoreceptor transplant restores vision in blind mice
Posted by: Great Ormond Street Hospital Children's Charity
18th April, 2012

GOSHCC Professor of Developmental Biology and Genetics, Jane Sowden,
is part of a research team who have shown for the first time that
transplanting light-sensitive photoreceptors into the eyes of visually
impaired mice can restore their vision.

She hopes this exciting development will pave the way for similar
approaches in humans, and clinical trials of new therapies to treat
degenerative and inherited retinal diseases that cause a third of
cases of childhood blindness.

 Transplanting photoreceptors

The research, led by Professor Robin Ali and a joint team at the UCL
Institute of Ophthalmology and the UCL Institute of Child Health (ICH)
(and published in Nature) suggests that transplanting photoreceptors -
the light-sensitive nerve cells that line the back of the eye - could
form the basis of a new treatment to restore sight in people with
degenerative eye diseases.

"The type of blindness we've been researching is common," says
Professor Jane Sowden, who heads up the ICH team: "Retinal diseases
that cause the loss of photoreceptor cells are one of the major causes
of untreatable blindness, which include inherited retinal diseases
that affect around 1 in 3000 people, and are responsible for around
the third of cases of childhood blindness."



"We have been aiming to develop new therapies for retinal diseases
which would involve transplanting new photoreceptor cells to replace
those that are lost through disease. Over the last decade we've been
developing ways to transplant photoreceptor cells into the retina. "

Remarkable tests

"In this new study we've been able to show that by transplanting
photoreceptors into the retina of mice who are born with a form of
blindness that the new cells are able to make connections that are
functional."

Not only this, but after four to six weeks, the transplanted cells
appeared to be functioning almost as well as normal photoreceptor
cells.  They had also formed the vital connections needed to transmit
visual information to other cells in the retina, and onwards to the
brain.

Jane continues: "We performed a number of different tests, but one of
the most remarkable was the fact that the treated animals were able to
navigate their way through a maze, whereas the untreated animals were
not, demonstrating that the cells were functioning. So the treated
animals were using this visual information to modify their behaviour."

Promise for the future

She thinks this shows exciting promise for future research and
potential treatments: "What we've shown for the first time is that the
transplantation of new photoreceptor cells can restore vision. What we
hope is that it will be possible to develop similar approaches for the
treatment of human blindness.

There are many steps we need to undertake before we're in a position
to do that, but based on the similarities between the mouse and the
human retina we think that this may be a future treatment for
currently untreatable retinal disease."

You can view the full Nature paper here.

The research was funded by the Medical Research Council, the Wellcome
Trust, the Royal Society, the British Retinitis Pigmentosa Society,
Alcon Research Institute and The Miller's Trust. Professor Jane Sowden
is funded by Great Ormond Street Hospital Children's Charity.

watch video clip:

Photoreceptor transplant restores vision in mice - Jane Sowden GOSHCC Professor

http://www.youtube.com/watch?v=U5Nn7eLFE0w&feature=player_embedded
Uploaded by GOSHCharity on Apr 18, 2012

GOSHCC Professor of Developmental Biology and Genetics, Jane Sowden,
is part of a research team who have shown for the first time that
transplanting light-sensitive photoreceptors into the eyes of visually
impaired mice can restore their vision. She hopes this exciting
development will pave the way for similar approaches in humans, and
clinical trials of new therapies to treat degenerative and inherited
retinal diseases that cause a third of cases of childhood blindness.

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