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A new study shows that, when properly
manipulated, a population of support cells found in
the brain called astrocytes could provide a new and
promising approach to treat Parkinson’s disease.
These findings, which were made using an animal
model of the disease, demonstrate that a single
therapy could simultaneously repair the multiple
types of neurological damage caused by
Parkinson’s, providing an overall benefit that has
not been achieved in other approaches.
approaches.
“One of the central challenges in Parkinson’s
disease is that many different cell types are
damaged, each of which is of potential
Proschel,
importance,” said Chris Proschel, Ph.D., an
assistant professor of Biomedical Genetics at the
University of Rochester Medical Center (URMC)
and lead author of the study which appears today
in the European journal EMBO Molecular
Medicine.
“However, while we know that the collective loss of
these cells contributes to the symptoms of the
disease, much of the current research is focused on
the recovery of only one cell type.”
type.”
Parkinson’s disease is a progressive neurological
disorder which affects an estimated one million
Americans.
While the condition is associated with the loss of
dopaminergic neurons – cells that produce the
important neurotransmitter dopamine – the
disease’s impact is actually far more complex and
widewide-ranging, disrupting basic signaling functions
and triggering the destruction of several other
types of cells found in the brain.
Consequently, while the preservation and
restoration of dopamine producing neurons is
critical to slowing or reversing the course of the
disease, it is increasingly clear that any successful
longlong-term therapy must both protect the areas of
the brain under attack and foster the repair of
not only dopaminergic neurons but also the
damage that occurs in other cell populations.
“Reversing the disease’s impact on the brain is
akin to the challenges of fixing a house that is in
Proschel.
the process of falling apart,” said Proschel. “If
you only focus on addressing one aspect of the
problem, such as the wiring, but ignore the fact
that the roof is leaking and the foundation is
crumbling, then you haven’t really carried out
the necessary repairs and it is only a matter of
time before the lights go out again.”
Using human brain cells, Proschel and his
colleagues isolated a cell population found in
the central nervous system called glial
precursors. Through the careful manipulation
of culture conditions and cell signals, the
researchers induced the precursor cells to
produce a specific class of astrocytes.
While astrocytes tend to garner far less attention than
their more glamorous cousin, the neuron, they
nevertheless are critical to maintaining a healthy
environment in the brain. On the flip side, scientists
are learning that astrocyte dysfunction can contribute
to multiple neurological disorders.
In both instances, the ability to realize the therapeutic
implications of these discoveries has proven to be
difficult. The ability of labs such as Proschel’s to isolate
and identify the unique properties of different kinds of
astroctyes, essentially finding the right cell for the right
astroctyes,
job, offers the possibility of harnessing these cells for
new therapies.
The astrocytes used in the study differ from other
types of astrocytes present in the mature brain.
When implanted into the brains of rats with
Parkinson’s disease, the new cells acted similar to
astrocytes found in the developing brain, which
are more effective at building connections
between nerves and creating a suitable
environment for growth and repair.
Consequently, the implanted astrocytes acted like
a repair crew, restoring the health and stability of
the structure and allowing the brain’s nerve cells
to recover and resume normal activity.
The researchers were careful to implant the
cells only after the rats had developed signs of
Parkinson’s disease.
This delay was important because it mimics
how a similar therapy would be used in
humans where the neurological damage caused
by the disease precedes its visible symptoms.
After transplantation, the researchers observed that
not only did dopaminergic neurons recover in the
animals, but other nerve cells called interneurons
were also rescued. Interneurons play an important
role in information processing and movement
control, and are also lost in Parkinson’s disease. No
previous therapies have rescued these cells.
Moreover, the therapy restored normal levels of
synaptophysin,
synaptophysin, a protein that is essential for
communication between nerve cells. The
transplanted rats recovered motor skills to normal
levels, essentially reversing the symptoms of the
disease.
“The central importance of this work is in revealing
a potentially new cell therapy, for which appropriate
human cells are in hand, that can be used to restore
multiple neuronal populations and to rescue the
molecular machinery critical in communication
between nerve cells even when cells are transplanted
after the damage is already established,”
said Mark Noble, Ph.D., the director of the URMC
Stem Cell and Regenerative Medicine Institute and a
coco-author of the study. “From what is already known
about these cells, it seems likely that they offer a
promising approach to a variety of neurological
afflictions.”
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Finding Points To Possible New Parkinson’s Therapy

  • 1.
  • 2. A new study shows that, when properly manipulated, a population of support cells found in the brain called astrocytes could provide a new and promising approach to treat Parkinson’s disease. These findings, which were made using an animal model of the disease, demonstrate that a single therapy could simultaneously repair the multiple types of neurological damage caused by Parkinson’s, providing an overall benefit that has not been achieved in other approaches. approaches.
  • 3. “One of the central challenges in Parkinson’s disease is that many different cell types are damaged, each of which is of potential Proschel, importance,” said Chris Proschel, Ph.D., an assistant professor of Biomedical Genetics at the University of Rochester Medical Center (URMC) and lead author of the study which appears today in the European journal EMBO Molecular Medicine. “However, while we know that the collective loss of these cells contributes to the symptoms of the disease, much of the current research is focused on the recovery of only one cell type.” type.”
  • 4. Parkinson’s disease is a progressive neurological disorder which affects an estimated one million Americans. While the condition is associated with the loss of dopaminergic neurons – cells that produce the important neurotransmitter dopamine – the disease’s impact is actually far more complex and widewide-ranging, disrupting basic signaling functions and triggering the destruction of several other types of cells found in the brain.
  • 5. Consequently, while the preservation and restoration of dopamine producing neurons is critical to slowing or reversing the course of the disease, it is increasingly clear that any successful longlong-term therapy must both protect the areas of the brain under attack and foster the repair of not only dopaminergic neurons but also the damage that occurs in other cell populations.
  • 6. “Reversing the disease’s impact on the brain is akin to the challenges of fixing a house that is in Proschel. the process of falling apart,” said Proschel. “If you only focus on addressing one aspect of the problem, such as the wiring, but ignore the fact that the roof is leaking and the foundation is crumbling, then you haven’t really carried out the necessary repairs and it is only a matter of time before the lights go out again.”
  • 7. Using human brain cells, Proschel and his colleagues isolated a cell population found in the central nervous system called glial precursors. Through the careful manipulation of culture conditions and cell signals, the researchers induced the precursor cells to produce a specific class of astrocytes.
  • 8. While astrocytes tend to garner far less attention than their more glamorous cousin, the neuron, they nevertheless are critical to maintaining a healthy environment in the brain. On the flip side, scientists are learning that astrocyte dysfunction can contribute to multiple neurological disorders. In both instances, the ability to realize the therapeutic implications of these discoveries has proven to be difficult. The ability of labs such as Proschel’s to isolate and identify the unique properties of different kinds of astroctyes, essentially finding the right cell for the right astroctyes, job, offers the possibility of harnessing these cells for new therapies.
  • 9. The astrocytes used in the study differ from other types of astrocytes present in the mature brain. When implanted into the brains of rats with Parkinson’s disease, the new cells acted similar to astrocytes found in the developing brain, which are more effective at building connections between nerves and creating a suitable environment for growth and repair. Consequently, the implanted astrocytes acted like a repair crew, restoring the health and stability of the structure and allowing the brain’s nerve cells to recover and resume normal activity.
  • 10. The researchers were careful to implant the cells only after the rats had developed signs of Parkinson’s disease. This delay was important because it mimics how a similar therapy would be used in humans where the neurological damage caused by the disease precedes its visible symptoms.
  • 11. After transplantation, the researchers observed that not only did dopaminergic neurons recover in the animals, but other nerve cells called interneurons were also rescued. Interneurons play an important role in information processing and movement control, and are also lost in Parkinson’s disease. No previous therapies have rescued these cells. Moreover, the therapy restored normal levels of synaptophysin, synaptophysin, a protein that is essential for communication between nerve cells. The transplanted rats recovered motor skills to normal levels, essentially reversing the symptoms of the disease.
  • 12. “The central importance of this work is in revealing a potentially new cell therapy, for which appropriate human cells are in hand, that can be used to restore multiple neuronal populations and to rescue the molecular machinery critical in communication between nerve cells even when cells are transplanted after the damage is already established,” said Mark Noble, Ph.D., the director of the URMC Stem Cell and Regenerative Medicine Institute and a coco-author of the study. “From what is already known about these cells, it seems likely that they offer a promising approach to a variety of neurological afflictions.”
  • 13. Discover The Truth About Parkinson's That Doctors And Pharmaceutical Companies Hope You Won't Find Out About Here: Click Here: http://goo.gl/o60yWZ