News release
For Immediate Release
October 3, 2005
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Professors Toshihide Yamashita and Zhigang He to Receive
2005
Ameritec Prize for Paralysis Research
The
Ameritec Foundation announced today that Dr.
Toshihide
Yamashita of Chiba
University in Japan and Dr. Zhigang He of Children’s Hospital, Harvard
Medical School, Boston, have been selected as the co-recipients of the
2005 Ameritec Prize for significant accomplishment toward a cure for
paralysis. The Prize recognizes Drs. Yamashita’s and He’s significant
contribution in the "demonstration
that multiple myelin inhibitors of
axonal regeneration mediate their actions by converging on a signaling
pathway involving members of the p75 receptor family.”
Drs. Yamashita and He
will receive the Prize at at a special recognition dinner in Washington
DC on November 13, 2005.
The Ameritec Foundation is a charitable, non-profit public benefit
foundation based in Covina, California. It provides funding for the
$40,000 prize. The winner is selected by a Scientific Advisory Board of
internationally known medical researchers.
The link
of inhibitory signals to the p75 receptor grew out of work by Dr.
Yamashita with previous Ameritec Prize winner Dr. Yves Barde, in which
they found an unexpected interaction of p75 with RhoA, a regulator of
the actin cytoskeleton. In a seminal piece of lateral thinking, Dr.
Yamashita and his colleagues explored whether this link of p75 to RhoA
might be relevant to the actions of Myelin Associated Glycoprotein (MAG),
a key myelin-derived inhibitor of neurite growth. Unexpectedly, their
experiments showed that p75 is actually required for MAG’s inhibitory
effects, and they went on to provide evidence that p75 transduces the
inhibitory signal.
Dr. He set
out to identify novel myelin-derived inhibitors of neurite extension.
Through biochemical and biological characterization of lipid-anchored
proteins in myelin, he and his colleagues first identified
Oligodendrocyte Myelin Glycoprotein (OMpg) as a novel myelin-derived
inhibitor, and made the surprising discovery that it binds NgR, a Nogo66
receptor identified by previous Ameritec Prize winner Dr. Steven
Strittmatter. Work by Dr. He and previous Ameritec prize winner Dr.
Marie Filbin, as well as by Dr. Strittmatter, had shown that MAG also
binds NgR. Putting together those observations with Dr. Yamashita’s
work, Dr. He and colleagues went on to show that NgR and p75 form a
receptor complex for all three of these inhibitors. The finding that
NgR and p75 form a receptor complex for MAG was also made by previous
Ameritec prize-winner Dr. Mu-ming Poo and his colleagues. The
identification by Dr. He of a third myelin-derived inhibitor, and his
demonstration that all three inhibitors (MAG, Nogo, and OMgp) can signal
via a NgR-p75 complex, provided a key generalization of Dr. Yamashita’s
findings. Collectively, this work has focused attention on this
signaling axis as a promising target for therapeutic interventions to
stimulate axonal regeneration following spinal cord injury.
Dr. He was
born in Jiangsu, China and earned his undergraduate degree in Medicine
in 1984 from Nanjing Medical University. He completed Ph.D. training in
1996 in the Department of Genetics at University of Toronto with
mentorship from Dr. James Ingles. He received the
Connaught
Scholarship, Medical Research Council of Canada Studentship and Ontario
Graduate Scholarship. He then moved to the University of California, San
Francisco for postdoctoral training with Dr. Marc Tessier-Lavigne in the
Howard Hughes Medical Institute and Department of Anatomy. Under the
supervision of Dr.Tessier-Lavinge, he identified neuropilin-1 as a
receptor of an axonal repulsive molecule Semaphorin3A. In 1999, he
became an Assistant Professor in the Division of Neuroscience at
Children’s Hospital Boston, Harvard Medical School. Since then, his lab
has been studying the cellular and molecular mechanisms of axon
regeneration.
FOR FUTHER
INFORMATION: Contact Bob Yant, Ameritec Prize Administrator, at 949
673-8474
Copyright © 2006 [Ameritec Foundation]. All rights reserved.
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