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Mary
Bartlett Bunge, is a Professor of Cell Biology
& Anatomy, Neurological Surgery and Neurology
at the University of Miami School of Medicine.
Her
major research interest is the development and
repair of nervous tissue. She and her team have
recently found that grafts of a specific type
of nerve cell, called Schwann cells, can provide
effective bridges. Bunge's team is currently investigating
what other cell types could be transplanted and
which factors could be added to the bridge or
spinal cord to improve the regenerative growth.
For her contribution to her field and the University
of Miami, Dr. Bunge is the recipient of numerous
awards, including the 1996 Wakeman Award, honoring
advancement of spinal cord injury research, the
Javits Neuroscience Investigator Award from the
NIH in 1998, and the University of Miami School
of Medicine's Senior Laboratory Research Award
in 1999. She was also the first winner of the
Mika Salpeter Women in Neuroscience Lifetime Achievement
Award in 2000.
Bunge
sits on the Council for the National Institute
of Neurological Disorders and Stroke (NINDS) and
is currently a member of the Dana Alliance for
Brain Initiatives and the Christopher Reeve Paralysis
Foundation Research Consortium.
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For
links to this scientist's home page and other related
infomation please see our resources
page.
Bunge
responds :
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4.17.01
Roxane Gross asked:
I had an episode of optic neuritis in my right
eye caused by Multiple Sclerosis last June. I
was told that due to the damage to the myelin
and to the nerve tissue of the optic nerve that
my sight probably would not return completely.
Is it possible, based on what I saw on the program
with the Schwann cells, that the nerve tissue
and the myelin can be restored in the optic nerve?
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Bunge's
response:
Roxane,
Some remyelination does occur naturally, but often
not complete repair. Even though Schwann cells
are not a normal component of the central nervous
system (CNS = brain, spinal cord, and, surprisingly,
optic nerve and retina!) we know that Schwann
cells can myelinate axons in the CNS, and often
do after injuries and in MS plaques.
All
that means that yes, it may be possible to use
Schwann cells to remyelinate optic nerve as well.
Many of the best known studies of Schwann cells
in rats have been conducted using the optic nerve
as a "model" to study re-growth of damaged axons.
While this has shown promise in the laboratory,
the regenerated/remyelinated axons are generally
treated immediately after the damage, and even
then, only about 10% of the retinal cells survive
and regenerate (when the optic nerve is completely
cut). With MS, the possibility of recurrent episodes
of demyelination also presents a problem.
To our knowledge, Schwann cell transplantation
into the optic nerve has not been attempted clinically
, and it is not advisable to assume that such
grafts should be tried on you (or anyone) at this
point. We now know that in MS, loss of function
is actually due to the nerve fiber damage at later
stages as well as demyelination; in this case
a therapy aimed at remyelination alone would not
be effective. Clinical trials are currently being
planned for use of Schwann cells in MS, but as
a first trial, not as a curative strategy at this
point. For more information, you might want to
check the web site for The
Myelin Project.
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4.17.01
Rick Smith asked:
Is there a chance that using Schwann cells might
help people with Tinnitus?
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Bunge's
response:
Rick,
To my knowledge the tinnitus is not caused by
the same types of nerve damage we are studying
in relation to Schwann cell implants. For more
information about Tinnitus, its causes and possible
treatments, you may want to visit the web site
of the American
Tinnitus Association, which I found quite
informative.
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4.17.01
Jim Barricklow asked:
Will Schwann cells work for people with brain
stem strokes?
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Bunge's
response:
Jim,
The damage caused by strokes is mostly due to
the loss of nerve cells themselves. In contrast,
most of the function lost after spinal cord injury,
as described in the program, is actually due to
damage of the extensions ("axons") of surviving
nerve cells. Because the axons are damaged, their
lines of communication are interrupted. The "brain
stem" is a name for a particular area of the brain,
so the rules it follows in disease and recovery
are no different.
It
seems likely at this time that more progress will
be made using stem cells (as described in the
first segment of the program) as a cellular therapy
for stroke than Schwann cells. Stem cells offer
the possibility of replacing those lost nerve
cells, and scientists are exploring whether the
brain (or in particular, the brain stem) is able
to guide the maturation of the nerve cells and
restoration of their connections needed to help
stroke patients.
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4.17.01
René asked:
Is your research going to be useful for multiple
sclerosis?
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Bunge's
response:
René
Yes, there is a very good chance that Schwann
cells could be helpful in treating some MS patients.
There is no very good animal model for MS now
because the disease itself is more complicated
than any of our models of demyelination. However,
we and some of our colleagues at Yale University
think that the time may be right to consider a
first trial of Schwann cells in the clinic. For
now such a trial would have to be aimed at the
safety of using these cells in the brain or spinal
cord, and assessing any evidence at all that a
very small graft (small for safety reasons) would
be able to remyelinate axons near an MS plaque.
The safety issue is especially important in a
progressive disease like MS where recurrences
are a possibility due to various causes. Again,
for more information, you might want to check
the web site for The Myelin Project, www.myelin.org
which is slated to sponsor the Yale trial. The
web site for more information regarding MS is
www.nmss.org.
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