Axonal responses to cellularly delivered NT=4/5 after spinal cord injury

被引:54
作者
Blesch, A
Yang, H
Weidner, N
Hoang, A
Otero, D
机构
[1] Univ Calif San Diego, Dept Neurosci 0626, La Jolla, CA 92093 USA
[2] Univ Regensburg, Dept Neurol, D-93053 Regensburg, Germany
关键词
D O I
10.1016/j.mcn.2004.06.007
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neurotrophic factors delivered to the injured spinal cord have been shown to enhance axonal growth, prevent neuronal degeneration and partially improve sensorimotor function. The present study examined the effects of NT-4/5 on growth of spinal and supraspinal axons, glia, and functional outcome after spinal cord injury. Adult Fischer 344 rats received spinal cord dorsal hemisections or complete transections at the midthoracic level. Fibroblasts modified to secrete NT-4/5 or green fluorescent protein as controls were immediately grafted to the lesion site. Axonal growth responses were determined between 3 and 6 months postinjury by retrograde and anterograde tracing and immunohistochemistry. Motor axons, coerulospinal, reticulospinal, and propriospinal axons responded to NT-4/5 delivery after thoracic spinal cord injury with significantly increased axonal penetration into NT-4/5 secreting grafts compared to C.FP-expressing control grafts. Axonal growth beyond NT-4/5-producing grafts and functional recovery were not observed. Numerous Schwann cells, but not oligodendrocytes, were present within NT-4/5-secreting grafts and remyelinated axons inside the graft. Thus, NT-4/5 and BDNF appear to be interchangeable to elicit substantial axonal growth in the injured spinal cord. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:190 / 201
页数:12
相关论文
共 34 条
[1]   A SENSITIVE AND RELIABLE LOCOMOTOR RATING-SCALE FOR OPEN-FIELD TESTING IN RATS [J].
BASSO, DM ;
BEATTIE, MS ;
BRESNAHAN, JC .
JOURNAL OF NEUROTRAUMA, 1995, 12 (01) :1-21
[2]  
Blesch A, 1999, J NEUROSCI, V19, P3556
[3]   Cellular GDNF delivery promotes growth of motor and dorsal column sensory axons after partial and complete spinal cord transections and induces remyelination [J].
Blesch, A ;
Tuszynski, MH .
JOURNAL OF COMPARATIVE NEUROLOGY, 2003, 467 (03) :403-417
[4]  
Blesch A, 1998, PROG BRAIN RES, V117, P473
[5]  
Blesch A, 2000, J NEUROSCI RES, V59, P402, DOI 10.1002/(SICI)1097-4547(20000201)59:3<402::AID-JNR14>3.3.CO
[6]  
2-H
[7]   NT-3, but not BDNF, prevents atrophy and death of axotomized spinal cord projection neurons [J].
Bradbury, EJ ;
King, V ;
Simmons, LJ ;
Priestley, JV ;
McMahon, SB .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1998, 10 (10) :3058-3068
[8]   Knocking the NT4 gene into the BDNF locus rescues BDNF deficient mice and reveals distinct NT4 and BDNF activities [J].
Fan, G ;
Egles, C ;
Sun, Y ;
Minichiello, L ;
Renger, JJ ;
Klein, R ;
Liu, GS ;
Jaenisch, R .
NATURE NEUROSCIENCE, 2000, 3 (04) :350-357
[9]   INSITU DEMONSTRATION OF MATURE OLIGODENDROCYTES AND THEIR PROCESSES - AN IMMUNOCYTOCHEMICAL STUDY WITH A NEW MONOCLONAL-ANTIBODY, RIP [J].
FRIEDMAN, B ;
HOCKFIELD, S ;
BLACK, JA ;
WOODRUFF, KA ;
WAXMAN, SG .
GLIA, 1989, 2 (05) :380-390
[10]  
Giehl KM, 1998, J NEUROSCI, V18, P7351