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Intrinsic Injury Signals Enhance Growth Survival and Excitability of Aplysia Neurons

机译:内在损伤信号增强海Ap神经元的生长存活和兴奋性

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摘要

Neurons undergo extensive changes in growth and electrophysiological properties in response to axon injury. Efforts to understand the molecular mechanisms that initiate these changes have focused almost exclusively on the role of extrinsic signals, primarily neurotrophic factors released from target and glial cells. The objective of the present investigation was to determine whether the response to axonal injury also involves intrinsic axoplasmic signals.Aplysia neurons were removed from their ganglia and placed in vitro on a substratum permissive for growth, but in the absence of glia and soluble growth factors. Under these conditions, neurites emerged and grew for ∼4 d. Once growth had ceased, the neurites were transected. In all, 46 of 50 cells regenerated, either by resorbing the remaining neurites and elaborating a new neuritic arbor or by merely replacing the neurites that had been severed. Cut cells also exhibited enhanced excitability and, paradoxically, prolonged survival, when compared with uninjured neurons. These findings indicate that axons contain intrinsic molecular signals that are directly activated by injury to trigger changes underlying regeneration and compensatory plasticity.
机译:神经元响应轴突损伤而经历生长和电生理特性的广泛变化。理解引发这些变化的分子机制的努力几乎完全集中在外在信号的作用上,主要是从靶细胞和神经胶质细胞释放的神经营养因子。本研究的目的是确定对轴突损伤的反应是否还涉及内在的轴质信号。将失眠神经元从其神经节中取出,并在体外放置在允许生长的基质上,但不存在神经胶质和可溶性生长因子。在这些条件下,神经突出现并生长约4天。生长停止后,将神经突切断。总共有50个细胞中有46个细胞是通过吸收剩余的神经突并形成新的神经轴或仅更换已切断的神经突来再生的。与未受伤的神经元相比,切细胞还表现出增强的兴奋性,并且自相矛盾地延长了生存期。这些发现表明,轴突包含固有的分子信号,该分子信号被损伤直接激活以触发潜在的再生和代偿性可塑性变化。

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