Shriners Hospitals Pediatric Research Center (Center for Neural Repair and Rehabilitation), Temple University School of Medicine, Philadelphia, PA; Department of Ophthalmology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Ann Neurol. 2013 Dec;74(6):768-77. doi: 10.1002/ana.24005. Epub 2013 Oct 7.
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.
中枢神经系统轴突损伤不仅导致损伤远端轴突的沃勒氏变性,还导致轴突切断神经元的死亡或萎缩,这取决于损伤部位和神经元类型。尽管对继发性神经元损伤的机制有广泛的了解,但仍未发现永久性避免这些变化的方法。神经元自主内质网(ER)应激途径最近被牵连到逆行神经元变性中。除了 ER 形态在轴突维持中的新兴作用外,我们还提出 ER 应激是神经元对轴突完整性紊乱的常见反应,也是神经退行性变的一般机制。因此,对内质网应激途径的操纵可能对神经保护具有重要的治疗意义。