Laboratory for NeuroRegeneration and Repair, Center for Neurology, Hertie Institute for Clinical Brain Research, University of Tuebingen, Otfried-Mueller Strasse 27, 72076, Tuebingen, Germany.
Neurotherapeutics. 2013 Oct;10(4):771-81. doi: 10.1007/s13311-013-0203-8.
Inadequate axonal sprouting and lack of regeneration limit functional recovery following neurologic injury, such as stroke, brain, and traumatic spinal cord injury. Recently, the enhancement of the neuronal regenerative program has led to promising improvements in axonal sprouting and regeneration in animal models of axonal injury. However, precise knowledge of the essential molecular determinants of this regenerative program remains elusive, thus limiting the choice of fully effective therapeutic strategies. Given that molecular regulation of axonal outgrowth and regeneration requires carefully orchestrated waves of gene expression, both temporally and spatially, epigenetic changes may be an ideal regulatory mechanism to address this unique need. While recent evidence suggests that epigenetic modifications could contribute to the regulation of axonal outgrowth and regeneration following axonal injury in models of stroke, and spinal cord and optic nerve injury, a number of unanswered questions remain. Such questions require systematic investigation of the epigenetic landscape between regenerative and non-regenerative conditions for the potential translation of this knowledge into regenerative strategies in human spinal and brain injury, as well as stroke.
轴突发芽不足和缺乏再生会限制神经损伤(如中风、脑和创伤性脊髓损伤)后的功能恢复。最近,神经元再生程序的增强导致了轴突损伤动物模型中轴突发芽和再生的有希望的改善。然而,这种再生程序的基本分子决定因素的精确知识仍然难以捉摸,从而限制了完全有效治疗策略的选择。鉴于轴突生长和再生的分子调控需要在时间和空间上精心协调基因表达的波,表观遗传变化可能是解决这一独特需求的理想调控机制。虽然最近的证据表明,表观遗传修饰可能有助于调节中风模型中轴突损伤后的轴突生长和再生,以及脊髓和视神经损伤,但仍有许多悬而未决的问题。这些问题需要对再生和非再生条件之间的表观遗传景观进行系统研究,以便将这些知识转化为人类脊髓和脑损伤以及中风的再生策略。