Extrinsic and intrinsic factors controlling axonal regeneration after spinal cord injury

被引:59
作者
Afshari, Fardad T. [1 ]
Kappagantula, Sunil [1 ]
Fawcett, James W. [1 ]
机构
[1] Univ Cambridge, Ctr Brain Repair, Cambridge CB2 0PY, England
来源
EXPERT REVIEWS IN MOLECULAR MEDICINE | 2009年 / 11卷
基金
英国医学研究理事会;
关键词
MYELIN-ASSOCIATED GLYCOPROTEIN; CENTRAL-NERVOUS-SYSTEM; CHONDROITIN SULFATE PROTEOGLYCANS; CELL-ADHESION MOLECULE; PROMOTES FUNCTIONAL RECOVERY; CORTICOSPINAL TRACT AXONS; ADULT SENSORY NEURONS; ROOT GANGLION NEURONS; NOGO-DEFICIENT MICE; NEURITE OUTGROWTH;
D O I
10.1017/S1462399409001288
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Spinal cord injury is one of the most devastating conditions that affects the central nervous system. It can lead to permanent disability and there are around two million people affected worldwide. After injury, accumulation of myelin debris and formation of an inhibitory glial scar at the site of injury leads to a physical and chemical barrier that blocks axonal growth and regeneration. The mammalian central nervous system thus has a limited intrinsic ability to repair itself after injury. To improve axonal outgrowth and promote functional recovery, it is essential to identify the various intrinsic and extrinsic factors controlling regeneration and navigation of axons within the inhibitory environment of the central nervous system. Recent advances in spinal cord research have opened new avenues for the exploration of potential targets for repairing the cord and improving functional recovery after trauma. Here, we discuss some of the important key molecules that could be harnessed for repairing spinal cord injury.
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页数:19
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