• Zixuan Cao, Ying Gao, Kangwen Deng, Gareth Williams, Patrick Doherty, and Frank S Walsh.
• Neuroscience Discovery, Wyeth Research, Princeton, NJ 08543, USA.
• Mol. Cell. Neurosci. 2010 Jan 1; 43 (1): 1-14.

AbstractMany studies have indicated that the inability of adult mammalian central nervous system (CNS) to regenerate after injury is partly due to the existence of growth-inhibitory molecules associated with CNS myelin. Studies over the years have led to the identification of multiple myelin-associated inhibitors, among which Nogo, myelin-associated glycoprotein (MAG) and oligodendrocyte-myelin glycoprotein (Omgp) represent potentially major contributors to CNS axon regeneration failure. Here we review in vitro and in vivo investigations into these inhibitory ligands and their functional mechanisms, focusing particularly on the neuronal receptors that mediate the inhibitory signals from these myelin molecules. A better understanding of the receptors for myelin-associated inhibitors could provide opportunities to decipher the mechanism of restriction in CNS regeneration, and lead to the development of potential therapeutic targets in neurodegenerative diseases and neurological injury. We will discuss the structures of the receptors and therapeutic opportunities that might arise based on this information.Copyright 2009 Elsevier Inc. All rights reserved.

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