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Neuregulin-1 (NRG1) plays a crucial role in axoglial signaling during the development of the peripheral nervous system, but its importance in adulthood after peripheral nerve injury remains unclear. We used single-neuron labeling with inducible Cre-mediated knock-out animals, which enabled visualization of a subset of adult myelinated sensory and motoneurons neurons in which Nrg1 was inducibly mutated by tamoxifen treatment. In uninjured mice, NRG1-deficient axons and the associated myelin sheath were normal, and the neuromuscular junction demonstrated normal apposition of presynaptic and postsynaptic components. After sciatic nerve crush, NRG1 ablation resulted in severe defects in remyelination: axons were either hypomyelinated or had no myelin sheath. NRG1-deficient axons were also found to regenerate at a slower rate. After nerve injury, the neuromuscular junction was reinnervated, but excess terminal sprouting was observed. Juxtacrine Neuregulin-1 signaling is therefore dispensable for maintenance of the myelin sheath in adult animals but has a key role in reparative processes after nerve injury.

Original publication

DOI

10.1523/JNEUROSCI.2568-10.2011

Type

Journal article

Journal

J Neurosci

Publication Date

02/03/2011

Volume

31

Pages

3225 - 3233

Keywords

Aging, Animals, Axons, Mice, Mice, Inbred C57BL, Mice, Knockout, Mice, Transgenic, Myelin Sheath, Nerve Fibers, Myelinated, Nerve Regeneration, Neuregulin-1, Neuromuscular Junction, Sciatic Neuropathy