Schwann Cell Role in Selectivity of Nerve Regeneration

被引:80
|
作者
Bolivar, Sara
Navarro, Xavier
Udina, Esther [1 ]
机构
[1] Univ Autonoma Barcelona, Inst Neurosci, Dept Cell Biol Physiol & Immunol, Bellaterra 08193, Spain
关键词
axon; Schwann cell; regeneration; axon-glia interactions; peripheral nerve injury; reinnervation accuracy; preferential motor reinnervation; motor; sensory; ELECTRICAL-STIMULATION PROMOTES; MYELIN-ASSOCIATED GLYCOPROTEIN; ADHESION MOLECULE L1; NEURON REGENERATION; FUNCTIONAL RECOVERY; POLYSIALIC ACID; MOTOR-NEURONS; L2/HNK-1; CARBOHYDRATE; AXONAL REGENERATION; NEUROTROPHIC FACTOR;
D O I
10.3390/cells9092131
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Peripheral nerve injuries result in the loss of the motor, sensory and autonomic functions of the denervated segments of the body. Neurons can regenerate after peripheral axotomy, but inaccuracy in reinnervation causes a permanent loss of function that impairs complete recovery. Thus, understanding how regenerating axons respond to their environment and direct their growth is essential to improve the functional outcome of patients with nerve lesions. Schwann cells (SCs) play a crucial role in the regeneration process, but little is known about their contribution to specific reinnervation. Here, we review the mechanisms by which SCs can differentially influence the regeneration of motor and sensory axons. Mature SCs express modality-specific phenotypes that have been associated with the promotion of selective regeneration. These include molecular markers, such as L2/HNK-1 carbohydrate, which is differentially expressed in motor and sensory SCs, or the neurotrophic profile after denervation, which differs remarkably between SC modalities. Other important factors include several molecules implicated in axon-SC interaction. This cell-cell communication through adhesion (e.g., polysialic acid) and inhibitory molecules (e.g., MAG) contributes to guiding growing axons to their targets. As many of these factors can be modulated, further research will allow the design of new strategies to improve functional recovery after peripheral nerve injuries.
引用
收藏
页码:1 / 18
页数:18
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