4.8 Article

Neuregulin-1 type III determines the ensheathment fate of axons

Journal

NEURON
Volume 47, Issue 5, Pages 681-694

Publisher

CELL PRESS
DOI: 10.1016/j.neuron.2005.08.017

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Funding

  1. NINDS NIH HHS [R01 NS029071-13S1, NS037475, NS26001, R01 NS029071-14, R01 NS026001, R01 NS029071-13, R01 NS029071-17, R01 NS029071, R01 NS029071-16, NS051282, R01 NS037475, NS17965, R01 NS017965, R01 NS051282, R01 NS029071-15, NS29071] Funding Source: Medline

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The signals that determine whether axons are ensheathed or myelinated by Schwann cells have long been elusive. We now report that threshold levels of neuregulin-1 (NRG1) type III on axons determine their ensheathment fate. Ensheathed axons express low levels whereas myelinated fibers express high levels of NRG1 type III. Sensory neurons from NRG1 type III deficient mice are poorly ensheathed and fail to myelinate; lentiviral-mediated expression of NRG1 type III rescues these defects. Expression also converts the normally unmyelinated axons of sympathetic neurons to myelination. Nerve fibers of mice haploinsufficient for NRG1 type III are disproportionately unmyelinated, aberrantly ensheathed, and hypomyelinated, with reduced conduction velocities. Type III is the sole NRG1 isoform retained at the axon surface and activates PI 3-kinase, which is required for Schwann cell myelination. These results indicate that levels of NRG1 type III, independent of axon diameter, provide a key instructive signal that determines the ensheathment fate of axons.

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