LINGO-1 antagonist promotes functional recovery and axonal sprouting after spinal cord injury

被引:164
作者
Ji, Benxiu
Li, Mingwei
Wu, Wu-Tian
Yick, Leung-Wah
Lee, Xinhua
Shao, Zhaohui
Wang, Joy
So, Kwok-Fai
McCoy, John M.
Pepinsky, R. Blake
Mi, Sha
Relton, Jane K.
机构
[1] Biogen Inc, Cambridge, MA 02142 USA
[2] Univ Hong Kong, Fac Med, Dept Anat, Hong Kong, Hong Kong, Peoples R China
关键词
D O I
10.1016/j.mcn.2006.08.003
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
LINGO-1 is a CNS-specific protein and a functional component of the NgR1/p75/LINGO-1 and NgR1/TAJ(TROY)/LINGO-1 signaling complexes that mediate inhibition of axonal outgrowth. These receptor complexes mediate the axonal growth inhibitory effects of Nogo, myelin-associated glycoprotein (MAG) and oligodendrocyte-myelin glycoprotein (OMgp) via RhoA activation. Soluble LINGO-1 (LINGO-1-Fc), which acts as an antagonist of these pathways by blocking LINGO-1 binding to NgR1, was administered to rats after dorsal or lateral hemisection of the spinal cord. LINGO-1-Fc treatment significantly improved functional recovery, promoted axonal sprouting and decreased RhoA activation and increased oligodendrocyte and neuronal survival after either rubrospinal or corticospinal tract transection. These experiments demonstrate an important role for LINGO-1 in modulating axonal outgrowth in vivo and that treatment with LINGO-1-Fc can significantly enhance recovery after spinal cord injury. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:311 / 320
页数:10
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