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The Journal of Neuroscience, November 21, 2007, 27(47):13000-13011; doi:10.1523/JNEUROSCI.3373-07.2007

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Development/Plasticity/Repair
Modulation of Semaphorin3A Activity by p75 Neurotrophin Receptor Influences Peripheral Axon Patterning

Ayal Ben-Zvi, Liat Ben-Gigi, Hagit Klein, and Oded Behar

The Hubert H. Humphrey Center for Experimental Medicine and Cancer Research, The Hebrew University Faculty of Medicine, Jerusalem 91120, Israel

Correspondence should be addressed to Oded Behar, The Hubert H. Humphrey Center for Experimental Medicine and Cancer Research, The Hebrew University Faculty of Medicine, P.O. Box 12272, Jerusalem 91120, Israel. Email: odedb{at}md.huji.ac.il

The p75 neurotrophin receptor (p75^NTR) interacts with multiple ligands and coreceptors. It is thought to mediate myelin growth inhibition as part of the Nogo receptor complex, in addition to its other roles. Paradoxically, however, peripheral axons of p75^{ExonIII–/–} mutant embryos are severely stunted. This inhibition of axon growth may be a result of neurite elongation defects in p75^NTR mutant neurons. Here, we show that p75^{ExonIII–/–} DRG neurons are hypersensitive to the repellent molecule Semaphorin3A (Sema3A). NGF modulates Sema3A activity equally well in both the p75^NTR mutant and wild-type neurons, indicating that the hypersensitivity of p75^NTR mutant neurons is probably not related to their NGF receptor activity. Neuropilin1 and p75^NTR partially colocalize in DRG growth cones. After Sema3A stimulation, the degree of colocalization is dramatically increased, particularly in clusters associated with Sema3A receptor complex activation. Coimmunoprecipitation studies show that p75^NTR interacts directly with the Sema3A receptors Neuropilin1 and PlexinA4. When coexpressed with both Neuropilin1 and PlexinA4, p75^NTR reduces the interaction between these two receptor components. Finally, p75^NTR/Sema3A double-mutant embryos show growth similar to that observed in Sema3A-null mice. These data indicate that p75^NTR is an important functional modulator of Sema3A activity and that, in the absence of p75^NTR, oversensitivity to Sema3A leads to severe reduction in sensory innervation. Our results also suggest that while inhibition of p75^NTR in CNS injury may enhance nerve regeneration resulting from the inhibition of myelin-associated protein, it may also inhibit nerve regeneration through its modulation of Sema3A.

Key words: axon guidance; development; dorsal root ganglion; DRG; knock-out mice; nerve growth factor; NGF; regeneration

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Received Nov. 1, 2006; revised Sept. 11, 2007; accepted Oct. 11, 2007.

Correspondence should be addressed to Oded Behar, The Hubert H. Humphrey Center for Experimental Medicine and Cancer Research, The Hebrew University Faculty of Medicine, P.O. Box 12272, Jerusalem 91120, Israel. Email: odedb{at}md.huji.ac.il

This article has been cited by other articles:

				L. C. Schecterson and M. Bothwell An All-Purpose Tool for Axon Guidance Sci. Signal., November 25, 2008; 1(47): pe50 - pe50. [Abstract] [Full Text] [PDF]

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