The Success and Failure of the Schwann Cell Response to Nerve Injury

被引:349
作者
Jessen, Kristjan R. [1 ]
Mirsky, Rhona [1 ]
机构
[1] UCL, Dept Cell & Dev Biol, London, England
基金
英国医学研究理事会; 英国惠康基金; 欧洲研究理事会;
关键词
PNS; repair cell; nerve injury; regeneration; c-Jun; re-programming; Schwann cell; PERIPHERAL-NERVE; C-JUN; AXONAL REGENERATION; FUNCTIONAL RECOVERY; WALLERIAN DEGENERATION; IN-VIVO; EXPERIMENTAL STRATEGIES; MOTONEURON SURVIVAL; NEGATIVE REGULATION; SIGNALING PATHWAY;
D O I
10.3389/fncel.2019.00033
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The remarkable plasticity of Schwann cells allows them to adopt the Remak (non-myelin) and myelin phenotypes, which are specialized to meet the needs of small and large diameter axons, and differ markedly from each other. It also enables Schwann cells initially to mount a strikingly adaptive response to nerve injury and to promote regeneration by converting to a repair-promoting phenotype. These repair cells activate a sequence of supportive functions that engineer myelin clearance, prevent neuronal death, and help axon growth and guidance. Eventually, this response runs out of steam, however, because in the long run the phenotype of repair cells is unstable and their survival is compromised. The re-programming of Remak and myelin cells to repair cells, together with the injury-induced switch of peripheral neurons to a growth mode, gives peripheral nerves their strong regenerative potential. But it remains a challenge to harness this potential and devise effective treatments that maintain the initial repair capacity of peripheral nerves for the extended periods typically required for nerve repair in humans.
引用
收藏
页码:1 / 14
页数:14
相关论文
共 131 条
[51]   Accelerated nerve regeneration in mice by upregulated expression of interleukin (IL) 6 and IL-6 receptor after trauma [J].
Hirota, H ;
Kiyama, H ;
Kishimoto, T ;
Taga, T .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (06) :2627-2634
[52]   Introduction to special issue: Challenges and opportunities for regeneration in the peripheral nervous system [J].
Hoeke, Ahmet ;
Brushart, Thomas .
EXPERIMENTAL NEUROLOGY, 2010, 223 (01) :1-4
[53]   Mechanisms of disease:: what factors limit the success of peripheral nerve regeneration in humans? [J].
Hoke, Ahmet .
NATURE CLINICAL PRACTICE NEUROLOGY, 2006, 2 (08) :448-454
[54]   Neuroprotection in the peripheral nervous system -: Rationale for more effective therapies [J].
Hoke, Ahmet .
ARCHIVES OF NEUROLOGY, 2006, 63 (12) :1681-1685
[55]   Dynamic Regulation of Schwann Cell Enhancers after Peripheral Nerve Injury [J].
Hung, Holly A. ;
Sun, Guannan ;
Keles, Sunduz ;
Svaren, John .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2015, 290 (11) :6937-6950
[56]   Chromatin-remodeling enzymes in control of Schwann cell development, maintenance and plasticity [J].
Jacob, Claire .
CURRENT OPINION IN NEUROBIOLOGY, 2017, 47 :24-30
[57]   Autophagic myelin destruction by schwann cells during wallerian degeneration and segmental demyelination [J].
Jang, So Young ;
Shin, Yoon Kyung ;
Park, So Young ;
Park, Joo Youn ;
Lee, Hye Jeong ;
Yoo, Young Hyun ;
Kim, Jong Kuk ;
Park, Hwan Tae .
GLIA, 2016, 64 (05) :730-742
[58]   The repair Schwann cell and its function in regenerating nerves [J].
Jessen, K. R. ;
Mirsky, R. .
JOURNAL OF PHYSIOLOGY-LONDON, 2016, 594 (13) :3521-3531
[59]   The origin and development of glial cells in peripheral nerves [J].
Jessen, KR ;
Mirsky, R .
NATURE REVIEWS NEUROSCIENCE, 2005, 6 (09) :671-682
[60]   Negative Regulation of Myelination: Relevance for Development, Injury, and Demyelinating Disease [J].
Jessen, Kristjan R. ;
Mirsky, Rhona .
GLIA, 2008, 56 (14) :1552-1565