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A Neutralizing Anti-Nogo66 Receptor Monoclonal Antibody Reverses Inhibition of Neurite Outgrowth by Central Nervous System Myelin.

Authors :
Weiwei Li
Walus, Lee
Rabacchi, Sylvia A.
Jirik, Adrienna
Chang, Ernie
Schauer, Jessica
Zheng, Betty H.
Benedetti, Nancy J.
Liu, Betty P.
Choi, Eugene
Worley, Dane
Silvian, Laura
Wenjun Mo
Mullen, Colleen
Weixing Yang
Strittmatter, Stephen M.
Sah, Dinah W. Y.
Pepinsky, Blake
Lee, Daniel H. S.
Source :
Journal of Biological Chemistry. 10/15/2004, Vol. 279 Issue 42, p43780-43788. 9p. 3 Charts, 4 Graphs.
Publication Year :
2004

Abstract

The Nogo66 receptor (NgR1) is a neuronal, leucine-rich repeat (LRR) protein that binds three central nervous system (CNS) myelin proteins, Nogo, myelin-associated glycoprotein, and oligodendrocyte myelin glycoprotein, and mediates their inhibitory effects on neurite growth. Although the LRR domains on NgR1 are necessary for binding to the myelin proteins, the exact epitope(s) involved in ligand binding is unclear. Here we report the generation and detailed characterization of an anti-NgR1 monoclonal antibody, 7E11. The 7E11 monoclonal antibody blocks Nogo, myelin-associated glycoprotein, and oligodendrocyte myelin glycoprotein binding to NgR1 with IC50 values of 120, 14, and 4.5 nM, respectively, and effectively promotes neurite out-growth of P3 rat dorsal root ganglia neurons cultured on a CNS myelin substrate. Further, we have defined the molecular epitope of 7E11 to be DNAQLR located in the third LRR domain of rat NgR1. Our data demonstrate that anti-NgR1 antibodies recognizing this epitope, such as 7E11, can neutralize CNS myelin-dependent inhibition of neurite outgrowth. Thus, specific anti-NgR1 antibodies may represent a useful therapeutic approach for promoting CNS repair after injury. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00219258
Volume :
279
Issue :
42
Database :
Academic Search Index
Journal :
Journal of Biological Chemistry
Publication Type :
Academic Journal
Accession number :
14890140
Full Text :
https://doi.org/10.1074/jbc.M401803200