Researchers at UT Southwestern Medical Center at Dallas have discovered a biochemical pathway that helps describe how neurons in the brain and spinal cord form their connections. Further study into the new data could lead to discoveries in nerve regrowth and regeneration. (Nature, 13-Sep-2001)
http://www.newswise.com/articles/2001/9/NEURONS.SWM.html
University of Texas Southwestern
Medical Center
RESEARCHERS AT UT SOUTHWESTERN DISCOVER
HOW NEURONS COMMUNICATE TO 'WIRE' DEVELOPING BRAIN
DALLAS - Sept. 13, 2001 - Researchers
at UT Southwestern Medical Center at Dallas have discovered a biochemical
pathway that helps describe how neurons in the brain and spinal cord form
their connections. Further study into the new data, published in today's
issue of Nature, could lead to discoveries in nerve regrowth and regeneration.
"By learning how nerve fibers grow
and form connections in the embryonic brain and spinal cord, we may ultimately
be able to determine how to coax nerves to regrow and regenerate," said
Dr. Mark Henkemeyer, assistant professor in the Center for Developmental
Biology at UT Southwestern.
The research focuses on a specific
group of receptors and ligands that are widely expressed in the developing
nervous system. Normally, ligands produced by one cell bind to their corresponding
receptor, which is expressed on target cells. This causes a change in the
receptor, allowing it to transduce signals into the receiving cell.
Although the body contains a vast
array of different classes of receptors and ligands, Henkemeyer and his
team have been working to learn how a particular group of such molecules,
the Eph receptors and ephrin ligands, communicate biochemical signals between
two cells.
Earlier discoveries by Henkemeyer
and his colleagues uncovered functions for the Ephs and ephrins in mice.
"We found that these molecules communicate
important signals that guide the growing tips of embryonic nerve fibers
(the axon growth cone) and, therefore, help form networks of neurons and
synapses in the brain in a process called axon pathfinding," Henkemeyer
said.
"We're trying to define the cellular
and biochemical basis of how neurons can establish all these connections."
The entire circuitry of the brain
and nervous system is controlled by this pathfinding, which leads to the
formation of intricate and highly precise connections.
"I like to view the brain as the
amazing organic supercomputer," Henkemeyer said. "But what's most amazing
is that, unlike the supercomputers that humans assemble with their hands,
neural networks, which are much more complicated than any man-made computer,
self-wire during embryonic and postnatal development. That's the big mystery
- trying to figure out how the nervous system self-wires.
"The key message of this present
study is something that we've been working on for many years. When I first
came to UT Southwestern to set up my laboratory, we realized that the Eph
receptors and ephrins are important partners in axon pathfinding. Before
then, everyone thought the ephrins were the ligands that bound to the Eph
receptor on the axon, which then turned on the axon pathfinding signal.
What I discovered, and what we continue to work on today, is that the ligands
- the ephrins themselves - are also receptors."
This finding was unprecedented, Henkemeyer
said. "For the most part, everyone thought ligands bind receptors and receptors
send signals, and, all of a sudden, we're saying, 'No, the receptor is
actually the ligand, and the ligand is the receptor.'"
Researchers then labeled the traditional
concept of the receptor-mediated signal as a "forward" signal to distinguish
it from the "reverse" signal that the ephrin ligands transduce into their
own cell.
"We laid out the hypothesis five
years ago that the ephrins were also receptors and that they transduce
what we call the 'reverse' signal, and we also proposed that the 'reverse'
signal was important in axon pathfinding," he said.
The present work now published in
Nature is an extension of the earlier description of "reverse" signaling.
The current study describes in detail the biochemical signal transduction
cascades that ephrins can transduce into their cell.
"Although a tremendous amount of
research remains to be carried out," Henkemeyer said, "we are one step
closer to figuring out how the brain and spinal cord wire themselves up."
The study represents five years'
worth of work by Henkemeyer and UT Southwestern Ph.D. candidate Chad Cowan,
who received the 2001 Nominata Award, the top award from the Southwestern
Graduate School of Biomedical Sciences, for his thesis research and studies.
The research was made possible by
support from the Kent Waldrep Center for Basic Research on Nerve Growth
and Regeneration and a grant from the Welch Foundation.
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Media Contact: Angela Genusa
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14-Sep-01
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