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Working with live rats whose optic nerve was damaged (a common model of central-nervous-system injury), Irwin, Benowitz and colleagues show that in the absence of Mst3b, axons show very little regeneration, even in the presence of factors known to enhance axon growth. In cell cultures, axon growth increased when activated Mst3b was expressed in the neurons.
"All the growth factors we've tested--oncomodulin, inosine, brain-derived neurotropic factor, nerve growth factor--act through Mst3b," says Benowitz. "In fact, activating Mst3b by itself is enough to cause growth even if there are no growth factors around. In terms of basic understanding of nerve cells, this is a very exciting finding."
Further studies examining how Mst3b exerts this growth-promoting effect may open up new avenues for treating brain and spinal cord injuries, Benowitz says. While this study explains why growth factors work--because they stimulate Mst3b--it's not yet known whether Mst3b is the best stimulator of axon growth from a practical drug-development standpoint, he adds.
Irwin is now working on possible gene therapy approaches involving Mst3b. Activating Mst3b may help overcome some natural "brakes" in the cell-signaling system that prevent nerve regeneration under normal conditions.
Barbara Lorber, PhD, formerly of Children's and now at the University of Cambridge (Cambridge, UK), was the paper's first author. NIH, the European Union, Alseres, Inc., and the Dr. Miriam and Sheldon G. Adelson Medical Research Foundation funded this study.
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