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Independent Control of Aging and Axon Regeneration

机译:衰老和轴突再生的独立控制

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Axon regeneration capacity often declines with age. One might assume that loss of regeneration is an obvious consequence of organismai aging. However, in the latest issue of Neuron, Byrne et al. (2014) demonstrate that regeneration ability and aging are regulated cell-autonomously within neurons, and can be decoupled.In animals, the juvenile state is often associated with better tissue-repair ability. Ample evidence suggests that this is also the case for axon regeneration, an essential step of neural repair after brain and spinal cord injury. For example, in contrast to immature neurons with robust growth ability, the terminally differentiated neurons in the adult mammalian central nervous system possess limited regenerative regrowth after injury. Such aging-associated decline of regenerative growth has also been observed in the mammalian peripheral nervous system and other species.
机译:轴突再生能力通常随年龄而下降。人们可能会认为再生的丧失是生物衰老的明显后果。然而,在最新一期的《神经元》中,伯恩(Byrne)等人。 (2014)证明了再生能力和衰老在神经元内由细胞自主调节,并且可以解耦。在动物中,幼年状态通常与更好的组织修复能力有关。大量证据表明,轴突再生也是这种情况,轴突再生是大脑和脊髓损伤后神经修复的重要步骤。例如,与具有强大生长能力的未成熟神经元相反,成年哺乳动物中枢神经系统中的终末分化神经元在受伤后具有有限的再生长生。在哺乳动物的外周神经系统和其他物种中也观察到了这种与衰老相关的再生生长下降。

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