Abstract
CNS myelin inhibits axonal outgrowth in vitro and is one of several obstacles to functional recovery following spinal cord injury. Central to our current understanding of myelin-mediated inhibition are the membrane protein Nogo and the Nogo-66 receptor (NgR). New findings implicate NgR as a point of convergence in signal transduction for several myelin-associated inhibitors. Additional studies have identified a potential coreceptor for NgR as p75(NTR), and a second-messenger pathway involving RhoA that inhibits neurite elongation. Although these findings expand our understanding of the molecular determinants of adult CNS axonal regrowth, the physiological roles of myelin-associated inhibitors in the intact adult CNS remain ill-defined.
MeSH terms
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Acute-Phase Proteins / metabolism
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Animals
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Axons / physiology*
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Cells, Cultured
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GPI-Linked Proteins
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Humans
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In Vitro Techniques
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Mice
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Myelin Proteins / classification
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Myelin Proteins / metabolism
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Myelin Proteins / physiology*
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Myelin Sheath / physiology*
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Myelin-Associated Glycoprotein / metabolism
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Myelin-Oligodendrocyte Glycoprotein
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Nerve Regeneration / physiology*
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Neural Inhibition / physiology*
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Neuronal Plasticity
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Nogo Proteins
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Nogo Receptor 1
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Rats
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Receptor, Nerve Growth Factor
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Receptors, Cell Surface / physiology*
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Receptors, Nerve Growth Factor / metabolism
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Signal Transduction / physiology
Substances
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Acute-Phase Proteins
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GPI-Linked Proteins
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MOG protein, human
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Mog protein, mouse
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Mog protein, rat
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Myelin Proteins
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Myelin-Associated Glycoprotein
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Myelin-Oligodendrocyte Glycoprotein
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Nogo Proteins
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Nogo Receptor 1
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RTN4 protein, human
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RTN4R protein, human
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Receptor, Nerve Growth Factor
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Receptors, Cell Surface
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Receptors, Nerve Growth Factor
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Rtn4 protein, mouse
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Rtn4 protein, rat
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Rtn4r protein, mouse
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Rtn4r protein, rat
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acute-phase protein rho