LINGO-1 negatively regulates myelination by oligodendrocytes

被引:502
作者
Mi, S
Miller, RH
Lee, X
Scott, ML
Shulag-Morskaya, S
Shao, ZH
Chang, JF
Thill, G
Levesque, M
Zhang, MD
Hession, C
Sah, D
Trapp, B
He, ZG
Jung, V
McCoy, JM
Pepinsky, RB
机构
[1] Biogen Idec Inc, Dept Discovery Biol, Cambridge, MA 02142 USA
[2] Case Western Reserve Univ, Sch Med, Dept Neurosci, Cleveland, OH 44106 USA
[3] Harvard Univ, Sch Med, Childrens Hosp, Div Neurosci, Boston, MA 02115 USA
[4] Cleveland Clin Fdn, Lerner Res Inst, Dept Neurosci, Cleveland, OH 44195 USA
关键词
D O I
10.1038/nn1460
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The control of myelination by oligodendrocytes in the CNS is poorly understood. Here we show that LINGO-1 is an important negative regulator of this critical process. LINGO-1 is expressed in oligodendrocytes. Attenuation of its function by dominant-negative LINGO-1, LINGO-1 RNA-mediated interference (RNAi) or soluble human LINGO-1 (LINGO-1-Fc) leads to differentiation and increased myelination competence. Attenuation of LINGO-1 results in downregulation of RhoA activity, which has been implicated in oligodendrocyte differentiation. Conversely, overexpression of LINGO-1 leads to activation of RhoA and inhibition of oligodendrocyte differentiation and myelination. Treatment of oligodendrocyte and neuron cocultures with LINGO-1-Fc resulted in highly developed myelinated axons that have internodes and well-defined nodes of Ranvier. The contribution of LINGO-1 to myelination was verified in vivo through the analysis of LINGO-1 knockout mice. The ability to recapitulate CNS myelination in vitro using LINGO-1 antagonists and the in vivo effects seen in the LINGO-1 knockout indicate that LINGO-1 signaling may be critical for CNS myelination.
引用
收藏
页码:745 / 751
页数:7
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