Sensory axon targeting is increased by NGF gene therapy within the lesioned adult femoral nerve

被引:28
作者
Hu, Xinhua [1 ]
Cai, Jie [1 ]
Yang, Jun [1 ]
Smith, George M. [1 ]
机构
[1] Univ Kentucky, Spinal Cord & Brain Injury Res Ctr, Dept Physiol, Lexington, KY 40536 USA
关键词
Femoral transection; Axon reinnervation; Recombinant adenovirus; Nerve growth factor; Axon guidance; Axon targeting; Triple retrograde tracing; GROWTH CONE GUIDANCE; SPINAL-CORD; LONG-TERM; PREFERENTIAL REINNERVATION; MOTOR AXONS; REGENERATION; PATHWAYS; AFFERENTS; NEURONS; FLUOROGOLD;
D O I
10.1016/j.expneurol.2009.08.025
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Even though peripheral nerves regenerate well, axons are often misrouted and reinnervate inappropriate distal pathways post-injury. Misrouting most likely occurs at branch points where regenerating axons make choices. Here, we show that the accuracy of sensory axon reinnervation is enhanced by overexpression of the guidance molecule nerve growth factor (NGF) distal to the bifurcation. We used the femoral nerve as a model, which contains both sensory and motor axons that intermingle in the parent trunk and distally segregate into the saphenous (SB) and motor branches (MB). Transection of the parent trunk resulted in misrouting of axon reinnervation to SB and MB. To enhance sensory axon targeting, recombinant adenovirus encoding NGF was injected along the SB close to the bifurcation 1 week post-injury. The accuracy of axon reinnervation was assessed by retrograde tracing at 3 or 8 weeks after nerve injury. NGF overexpression significantly increased the accuracy of SB axon reinnervation to the appropriate nerve branch, in a manner independent of enhancing axon regeneration. This novel finding provides in vivo evidence that gradient expression of neurotrophin can be used to enhance targeting of distal peripheral pathways to increase axon regeneration into the appropriate nerve branch. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:153 / 165
页数:13
相关论文
共 46 条
[1]   One hour electrical stimulation accelerates functional recovery after femoral nerve repair [J].
Ahlborn, Peter ;
Schachner, Melitta ;
Irintchev, Andrey .
EXPERIMENTAL NEUROLOGY, 2007, 208 (01) :137-144
[2]   Improved detection of fluorogold-labeled neurons in long-term studies [J].
Akhavan, M ;
Hoang, TX ;
Havton, LA .
JOURNAL OF NEUROSCIENCE METHODS, 2006, 152 (1-2) :156-162
[3]   Regulation of NGF-family ligands and receptors in adulthood and senescence: correlation to degenerative and regenerative changes in cutaneous innervation [J].
Bergman, E ;
Ulfhake, B ;
Fundin, BT .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2000, 12 (08) :2694-2706
[4]   Electrical stimulation restores the specificity of sensory axon regeneration [J].
Brushart, TM ;
Jari, R ;
Verge, V ;
Rohde, C ;
Gordon, T .
EXPERIMENTAL NEUROLOGY, 2005, 194 (01) :221-229
[5]  
Brushart TM, 2002, J NEUROSCI, V22, P6631
[6]  
BRUSHART TME, 1988, J NEUROSCI, V8, P1026
[7]   MOTOR AXONS PREFERENTIALLY REINNERVATE MOTOR PATHWAYS [J].
BRUSHART, TME .
JOURNAL OF NEUROSCIENCE, 1993, 13 (06) :2730-2738
[8]  
Cajal RY., 1928, DEGENERATION REGENER
[9]   Genetic manipulation of intraspinal plasticity after spinal cord injury alters the severity of autonomic dysreflexia [J].
Cameron, AA ;
Smith, GM ;
Randall, DC ;
Brown, DR ;
Rabchevsky, AG .
JOURNAL OF NEUROSCIENCE, 2006, 26 (11) :2923-2932
[10]   The Hedgehog, TGF-β/BMP and Wnt families of morphogens in axon guidance [J].
Charron, Frederic ;
Tessier-Lavigne, Marc .
AXON GROWTH AND GUIDANCE, 2007, 621 :116-133