Scheib Jami, Höke Ahmet
Departments of Neurology and Neuroscience, Johns Hopkins School of Medicine, Baltimore, MD 21205, USA.
Departments of Neurology and Neuroscience, Johns Hopkins School of Medicine, Baltimore, MD 21205, USA.
Exp Neurol. 2016 Oct;284(Pt A):79-83. doi: 10.1016/j.expneurol.2016.07.010. Epub 2016 Jul 21.
Although many observational studies have shown that peripheral nerve regeneration is impaired with aging, underlying cellular and molecular mechanisms have remained obscure until recently. A series of recent genetic, live imaging and heterochronic parabiosis experiments are providing new insights into the underlying mechanisms of reduced regenerative capacity with aging. These studies show that Schwann cells pose a primary impediment to axon regeneration in older animals as they fail to support regenerating axons, while the contribution from macrophages remains an unresolved issue. Neurons do not appear to have an intrinsic defect of axonal elongation with aging but are impaired when they encounter an inhibitory environment, suggesting that therapeutic approaches to improve intrinsic neuronal regeneration capacity across inhibitory environments, as it is being done in central nervous system regeneration, can improve peripheral nerve regeneration as well. As in many aspects of neuroscience therapeutics development, a combinatorial approach may yield the best outcomes for nerve regeneration in aged individuals.
尽管许多观察性研究表明,周围神经再生会随着年龄增长而受损,但直到最近,其潜在的细胞和分子机制仍不清楚。最近一系列的遗传学、实时成像和异时联体共生实验,正在为衰老导致再生能力下降的潜在机制提供新的见解。这些研究表明,雪旺细胞是老年动物轴突再生的主要障碍,因为它们无法支持再生轴突,而巨噬细胞的作用仍是一个未解决的问题。神经元似乎不会因衰老而出现轴突伸长的内在缺陷,但当它们遇到抑制性环境时就会受损,这表明,如同在中枢神经系统再生中所做的那样,通过治疗方法来提高神经元在抑制性环境中的内在再生能力,也可以改善周围神经再生。与神经科学治疗学发展的许多方面一样,联合治疗方法可能会为老年个体的神经再生带来最佳效果。