Neuregulin-1 type III determines the ensheathment fate of axons

被引:568
作者
Taveggia, C
Zanazzi, G
Petrylak, A
Yano, H
Rosenbluth, J
Einheber, S
Xu, XR
Esper, RM
Loeb, JA
Shrager, P
Chao, MV
Falls, DL
Role, L
Salzer, JL
机构
[1] NYU, Sch Med, Dept Cell Biol, New York, NY 10016 USA
[2] NYU, Sch Med, Dept Neurol, New York, NY 10016 USA
[3] NYU, Sch Med, Mol Neurobiol Program, Skirball Inst Biomol Med, New York, NY 10016 USA
[4] NYU, Sch Med, Dept Physiol, New York, NY 10016 USA
[5] NYU, Sch Med, Dept Neurosci, New York, NY 10016 USA
[6] NYU, Sch Med, Rusk Inst, New York, NY 10016 USA
[7] CUNY Hunter Coll, Sch Hlth Sci, New York, NY 10010 USA
[8] Univ Rochester, Med Ctr, Dept Neurobiol & Anat, Rochester, NY 14642 USA
[9] Univ Rochester, Med Ctr, Dept Biochem & Biophys, Rochester, NY 14642 USA
[10] Wayne State Univ, Sch Med, Dept Neurol, Detroit, MI 48201 USA
[11] Wayne State Univ, Sch Med, Ctr Mol Med & Genet, Detroit, MI 48201 USA
[12] Emory Univ, Sch Med, Dept Cell Biol, Atlanta, GA 30322 USA
[13] Columbia Univ Coll Phys & Surg, Ctr Neurobiol & Behav, New York, NY 10032 USA
关键词
D O I
10.1016/j.neuron.2005.08.017
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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.
引用
收藏
页码:681 / 694
页数:14
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