Axonal regeneration and functional recovery after complete spinal cord transection in rats by delayed treatment with transplants and neurotrophins

被引:296
作者
Coumans, JV [1 ]
Lin, TTS [1 ]
Dai, HN [1 ]
MacArthur, L [1 ]
McAtee, M [1 ]
Nash, C [1 ]
Bregman, BS [1 ]
机构
[1] Georgetown Univ, Med Ctr, Dept Neurosci, Washington, DC 20007 USA
关键词
spinal cord injury; CNS regeneration; functional recovery; neurotrophins; fetal transplants; chronic injury;
D O I
10.1523/JNEUROSCI.21-23-09334.2001
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Little axonal regeneration occurs after spinal cord injury in adult mammals. Regrowth of mature CNS axons can be induced, however, by altering the intrinsic capacity of the neurons for growth or by providing a permissive environment at the injury site. Fetal spinal cord transplants and neurotrophins were used to influence axonal regeneration in the adult rat after complete spinal cord transection at a midthoracic level. Transplants were placed into the lesion cavity either immediately after transection (acute injury) or after a 2-4 week delay (delayed or chronic transplants), and either vehicle or neurotrophic factors were administered exogenously via an implanted minipump. Host axons grew into the transplant in all groups. Surprisingly, regeneration from supraspinal pathways and recovery of motor function were dramatically increased when transplants and neurotrophins were delayed until 2-4 weeks after transection rather than applied acutely. Axonal growth back into the spinal cord below the lesion and transplants was seen only in the presence of neurotrophic factors. Furthermore, the restoration of anatomical connections across the injury site was associated with recovery of function with animals exhibiting plantar foot placement and weight-supported stepping. These findings suggest that the opportunity for intervention after spinal cord injury may be greater than originally envisioned and that CNS neurons with long-standing injuries can reinitiate growth, leading to improvement in motor function.
引用
收藏
页码:9334 / 9344
页数:11
相关论文
共 66 条
[51]  
Ribotta MGY, 2000, J NEUROSCI, V20, P5144
[52]   AXONS FROM CNS NEURONS REGENERATE INTO PNS GRAFTS [J].
RICHARDSON, PM ;
MCGUINNESS, UM ;
AGUAYO, AJ .
NATURE, 1980, 284 (5753) :264-265
[53]   REGENERATION OF LONG SPINAL AXONS IN THE RAT [J].
RICHARDSON, PM ;
ISSA, VMK ;
AGUAYO, AJ .
JOURNAL OF NEUROCYTOLOGY, 1984, 13 (01) :165-182
[54]   PERIPHERAL INJURY ENHANCES CENTRAL REGENERATION OF PRIMARY SENSORY NEURONS [J].
RICHARDSON, PM ;
ISSA, VMK .
NATURE, 1984, 309 (5971) :791-793
[55]   LESIONED CORTICOSPINAL TRACT AXONS REGENERATE IN MYELIN-FREE RAT SPINAL-CORD [J].
SAVIO, T ;
SCHWAB, ME .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (11) :4130-4133
[56]   AXONAL REGENERATION IN THE RAT SPINAL-CORD PRODUCED BY AN ANTIBODY AGAINST MYELIN-ASSOCIATED NEURITE GROWTH-INHIBITORS [J].
SCHNELL, L ;
SCHWAB, ME .
NATURE, 1990, 343 (6255) :269-272
[57]   SPROUTING AND REGENERATION OF LESIONED CORTICOSPINAL TRACT FIBERS IN THE ADULT-RAT SPINAL-CORD [J].
SCHNELL, L ;
SCHWAB, ME .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1993, 5 (09) :1156-1171
[58]  
SCHWAB ME, 1991, J NEUROSCI, V11, P709
[59]   INHIBITORS OF NEURITE GROWTH [J].
SCHWAB, ME ;
KAPFHAMMER, JP ;
BANDTLOW, CE .
ANNUAL REVIEW OF NEUROSCIENCE, 1993, 16 :565-595
[60]   Neurite growth inhibitors restrict plasticity and functional recovery following corticospinal tract lesions [J].
Thallmair, M ;
Metz, GAS ;
Z'Graggen, WJ ;
Raineteau, O ;
Kartje, GL ;
Schwab, ME .
NATURE NEUROSCIENCE, 1998, 1 (02) :124-131