http://www.sciencedirect.com/science/article/pii/S0304416517301915
Highlights
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- Neuronal intrinsic pathways for axonal regeneration/sprouting after injury.
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- Intracellular/extracellular promoters/inhibitors for axonal regeneration
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- Proteoglycan and its neuronal cell surface receptors as major inhibitors
Abstract
Background
Therapeutics
specific to neural injury have long been anticipated but remain
unavailable. Axons in the central nervous system do not readily
regenerate after injury, leading to dysfunction of the nervous system.
This failure of regeneration is due to both the low intrinsic capacity
of axons for regeneration and the various inhibitors emerging upon
injury. After many years of concerted efforts, however, these hurdles to
axon regeneration have been partially overcome.
Scope of review
This
review summarizes the mechanisms regulating axon regeneration. We
highlight proteoglycans, particularly because it has become increasingly
clear that these proteins serve as critical regulators for axon
regeneration.
Major conclusions
Studies
on proteoglycans have revealed that glycans not only assist in the
modulation of protein functions but also act as main players—e.g., as
functional ligands mediating intracellular signaling through specific
receptors on the cell surface. By regulating clustering of the
receptors, glycans in the proteoglycan moiety, i.e., glycosaminoglycans,
promote or inhibit axon regeneration. In addition, proteoglycans are
involved in various types of neural plasticity, ranging from synaptic
plasticity to experience-dependent plasticity.
General significance
Although
studies on proteins have progressively facilitated our understanding of
the nervous system, glycans constitute a new frontier for further
research and development in this field. This article is part of a
Special Issue entitled Neuro-glycoscience, edited by Kenji Kadomatsu and
Hiroshi Kitagawa.
Keywords
- Axon regeneration;
- Proteoglycans;
- Glycosaminoglycans;
- Neural plasticity
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