Neuronal Endoplasmic Reticulum Stress in Axon Injury and Neurodegeneration

被引:51
|
作者
Li, Shaohua [1 ,2 ]
Yang, Liu [1 ]
Selzer, Michael E. [1 ,3 ]
Hu, Yang [1 ]
机构
[1] Temple Univ, Sch Med, Shriners Hosp Pediat Res Ctr, Ctr Neural Repair & Rehabil, Philadelphia, PA 19140 USA
[2] Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Dept Ophthalmol, Wuhan 430074, Peoples R China
[3] Temple Univ, Sch Med, Dept Neurol, Philadelphia, PA 19140 USA
关键词
SPINAL-CORD-INJURY; RETINAL GANGLION-CELLS; ER-STRESS; SELF-DESTRUCTION; OPTIC-NERVE; OXIDATIVE STRESS; NEUROTROPHIC FACTOR; UNFOLDED PROTEINS; PROTECTS BRAIN; DELAYED DEATH;
D O I
10.1002/ana.24005
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Injuries to central nervous system axons result not only in Wallerian degeneration of the axon distal to the injury, but also in death or atrophy of the axotomized neurons, depending on injury location and neuron type. No method of permanently avoiding these changes has been found, despite extensive knowledge concerning mechanisms of secondary neuronal injury. The autonomous endoplasmic reticulum (ER) stress pathway in neurons has recently been implicated in retrograde neuronal degeneration. In addition to the emerging role of ER morphology in axon maintenance, we propose that ER stress is a common neuronal response to disturbances in axon integrity and a general mechanism for neurodegeneration. Thus, manipulation of the ER stress pathway could have important therapeutic implications for neuroprotection. Ann Neurol 2013;74:768-777
引用
收藏
页码:768 / 777
页数:10
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