PERIPHERAL AXON REGROWTH: NEW MOLECULAR APPROACHES

被引:51
作者
Christie, K. J.
Zochodne, D.
机构
[1] Univ Calgary, Dept Clin Neurosci, Calgary, AB T2N 4N1, Canada
[2] Univ Calgary, Hotchkiss Brain Inst, Calgary, AB T2N 4N1, Canada
基金
加拿大健康研究院;
关键词
peripheral nerve regeneration; PTEN; nerve injury; NERVE GROWTH-FACTOR; ELECTRICAL-STIMULATION PROMOTES; MONOCYTE CHEMOATTRACTANT PROTEIN-1; GLYCOGEN-SYNTHASE KINASE-3-BETA; SCHWANN-CELL DIFFERENTIATION; PRIMARY SENSORY NEURONS; REGENERATION IN-VIVO; GENE-RELATED PEPTIDE; DORSAL-ROOT GANGLIA; TENSIN-HOMOLOG PTEN;
D O I
10.1016/j.neuroscience.2013.02.059
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Peripheral nerves, essential connections between the brain, spinal cord and body, do not regenerate as well as generally reported. Identifying new strategies to facilitate regeneration is essential to reversing neurological deficits from nerve injuries or disease. This review will discuss several selected and novel molecular insights into peripheral nerve trunk repair and axon regrowth that have the potential to improve regenerative success. Of particular interest is the phosphatidylinositol 3-kinase (PI3K)-Akt pathway in peripheral neurons, inhibited by the constitutively expressed phosphatase tumor suppressor PTEN. Knockdown or inhibition of PTEN is associated with robust sprouting of adult sensory neurons in vitro and in vivo, additive to the accelerated outgrowth offered by the preconditioning effect. This sprouting response, if spatially and temporally constrained, may provide potent regrowth initiation, of interest in otherwise untreatable nerve damage. (C) 2013 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:310 / 324
页数:15
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