Enriched conditioning expands the regenerative ability of sensory neurons after spinal cord injury via neuronal intrinsic redox signaling

被引:40
作者
De Virgiliis, Francesco [1 ]
Hutson, Thomas H. [1 ]
Palmisano, Ilaria [1 ]
Amachree, Sarah [1 ]
Miao, Jian [1 ]
Zhou, Luming [1 ]
Todorova, Rositsa [1 ]
Thompson, Richard [2 ]
Danzi, Matt C. [3 ]
Lemmon, Vance P. [3 ]
Bixby, John L. [3 ]
Wittig, Ilka [4 ]
Shah, Ajay M. [2 ]
Di Giovanni, Simone [1 ,5 ]
机构
[1] Imperial Coll London, Dept Brain Sci, Div Neurosci, London, England
[2] Kings Coll London, British Heart Fdn Ctr, James Black Ctr, Sch Cardiovasc Med & Sci, London, England
[3] Univ Miami, Ctr Computat Sci, Miami Project Cure Paralysis, Miami, FL 33136 USA
[4] Goethe Univ, Fac Med, Funct Prote, Frankfurt, Germany
[5] Univ Tubingen, Ctr Neurol, Hertie Inst Clin Brain Res, Lab NeuroRegenerat & Repair, Tubingen, Germany
关键词
PROTEIN-KINASE-C; CENTRAL-NERVOUS-SYSTEM; AXON REGENERATION; NADPH OXIDASE; LOCOMOTOR RECOVERY; GENE-EXPRESSION; REACTIVE OXYGEN; OUTGROWTH; STAT3; CELL;
D O I
10.1038/s41467-020-20179-z
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Pre conditioning injury or environmental enrichment have been shown to promote axon regeneration. Here the authors show that environmental enrichment, combined with preconditioning injury promotes regeneration via a redox signalling dependent mechanism. Overcoming the restricted axonal regenerative ability that limits functional repair following a central nervous system injury remains a challenge. Here we report a regenerative paradigm that we call enriched conditioning, which combines environmental enrichment (EE) followed by a conditioning sciatic nerve axotomy that precedes a spinal cord injury (SCI). Enriched conditioning significantly increases the regenerative ability of dorsal root ganglia (DRG) sensory neurons compared to EE or a conditioning injury alone, propelling axon growth well beyond the spinal injury site. Mechanistically, we established that enriched conditioning relies on the unique neuronal intrinsic signaling axis PKC-STAT3-NADPH oxidase 2 (NOX2), enhancing redox signaling as shown by redox proteomics in DRG. Finally, NOX2 conditional deletion or overexpression respectively blocked or phenocopied enriched conditioning-dependent axon regeneration after SCI leading to improved functional recovery. These studies provide a paradigm that drives the regenerative ability of sensory neurons offering a potential redox-dependent regenerative model for mechanistic and therapeutic discoveries.
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页数:16
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