Epigenetic Regulation of Axon Outgrowth and Regeneration in CNS Injury: The First Steps Forward

被引:29
|
作者
Lindner, Ricco [1 ]
Puttagunta, Radhika [1 ]
Di Giovanni, Simone [1 ]
机构
[1] Univ Tubingen, Hertie Inst Clin Brain Res, Ctr Neurol, Lab NeuroRegenerat & Repair, D-72076 Tubingen, Germany
关键词
Epigenetics; Axonal regeneration; Histone modifications; DNA methylation; Spinal cord injury; Optic nerve crush; DNA METHYLTRANSFERASES DNMT3A; MESSENGER-RNA EXPRESSION; CENTRAL-NERVOUS-SYSTEM; BETA-II-TUBULIN; NF-KAPPA-B; SPINAL-CORD; RETT-SYNDROME; HISTONE DEACETYLASES; TRANSCRIPTION FACTOR; CHROMATIN REGULATION;
D O I
10.1007/s13311-013-0203-8
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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.
引用
收藏
页码:771 / 781
页数:11
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