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The Journal of Neuroscience, August 20, 2003, 23(20):7602-7609
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Semaphorin 3F Antagonizes Neurotrophin-Induced Phosphatidylinositol 3-Kinase and Mitogen-Activated Protein Kinase Kinase Signaling: A Mechanism for Growth Cone Collapse
Jasvinder K. Atwal,2,3
Karun K. Singh,1
Marc Tessier-Lavigne,3
Freda D. Miller,1,2 and
David R. Kaplan1,2
1The Hospital for Sick Children, Department of
Molecular and Medical Genetics, University of Toronto, Toronto, Ontario,
Canada M5G 1X8, 2Brain Tumor Research Center and
Center for Neuronal Survival, Montreal Neurological Institute, Montreal,
Quebec, Canada H3A 2B4, and 3Howard Hughes Medical
Institute and Department of Biological Sciences, Stanford University,
Stanford, California 94305-5020
Peripheral nerve growth is regulated by the coordinated action of numerous
external stimuli, including positively acting neurotrophin-derived growth cues
and restrictive semaphorin cues. Here, we show that Semaphorin 3F (Sema 3F)
can antagonize nerve growth factor (NGF)-stimulated TrkA (tyrosine receptor
kinase A) signaling in sympathetic neurons, thereby apparently contributing to
growth cone collapse. Sema 3F suppressed NGF-induced activation of the
phosphatidylinositol 3 (PI3)-kinase-Akt and MEK (mitogen-activated protein
kinase kinase)-ERK (extracellular signal-regulated kinase) pathways, both of
which we show to be required to maintain growth cone structure. Sema
3F-induced growth cone collapse was partially reversed by sustained activation
of the PI3-kinase and MEK pathways, which was achieved by overexpression of
the Gab-1 (growth-associated binder 1) docking protein. These data indicate
that a novel mechanism used by Sema 3F to collapse growth cones in sympathetic
neurons is to dampen neurotrophin signaling, providing an intracellular
mechanism for cross talk between positive and negative axon growth cues.
Key words: growth cone; semaphorin 3F; nerve growth factor; PI3-kinase; MEK; TrkA; signal transduction
Received Nov. 27, 2002;
revised Jun. 25, 2003;
accepted Jun. 26, 2003.
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