Present situation and future aspects of spinal cord regeneration

被引:22
作者
Enomoto, M [1 ]
Wakabayashi, Y [1 ]
Qi, ML [1 ]
Shinomiya, K [1 ]
机构
[1] Tokyo Med & Dent Univ, Dept Orthopaed & Spinal Surg, Bunkyo Ku, Tokyo 1138519, Japan
关键词
axonal regeneration; neurotrophic factors; chondroitin sulfate proteoglycans; neural stem cells; transplantation;
D O I
10.1007/s00776-003-0740-9
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
The central nervous system (CNS) has a limited capacity for regeneration after injury. In spinal cord injury (SCI) patients, total loss of all motor and sensory function occurs below the level of injury. Advances in treatment are expected for orthopedic and spinal surgeons. Recently, evidence of axonal regeneration and functional recovery has been reported in animal spinal cord injury models. Our studies on the roles of inhibitory molecules with a comparison between neonatal and adult animals may help serve as therapeutic targets to enhance axonal regeneration for the injured spinal cord. Also, our cell replacement study indicates the possibility of transplanting neural stem cells to supply the cell source for immature oligodendrocytes, which are thought to be essential for both the myelination and trophic support of regenerating axons in the spinal cord. Administration of neurotrophic factors, prevention of inhibitory factors, and stem cell technology have clinical applications in SCI patients. However, spinal cord regeneration involves a multistep process, and several factors have to be controlled after injury. A combination of several treatments could overcome a nonpermissive environment for spinal cord regeneration. Further understanding of the mechanisms and finding optimal targets of spinal cord regeneration are necessary to obtain successful therapies for SCI patients.
引用
收藏
页码:108 / 112
页数:5
相关论文
共 28 条
[1]   RECOVERY FROM SPINAL-CORD INJURY MEDIATED BY ANTIBODIES TO NEURITE GROWTH-INHIBITORS [J].
BREGMAN, BS ;
KUNKELBAGDEN, E ;
SCHNELL, L ;
DAI, HN ;
GAO, D ;
SCHWAB, ME .
NATURE, 1995, 378 (6556) :498-501
[2]   Stem cell repair of central nervous system injury [J].
Cao, QL ;
Benton, RL ;
Whittemore, SR .
JOURNAL OF NEUROSCIENCE RESEARCH, 2002, 68 (05) :501-510
[3]   Nogo-A is a myelin-associated neurite outgrowth inhibitor and an antigen for monoclonal antibody IN-1 [J].
Chen, MS ;
Huber, AB ;
van der Haar, ME ;
Frank, M ;
Schnell, L ;
Spillmann, AA ;
Christ, F ;
Schwab, ME .
NATURE, 2000, 403 (6768) :434-439
[4]   Regeneration of adult axons in white matter tracts of the central nervous system [J].
Davies, SJA ;
Fitch, MT ;
Memberg, SP ;
Hall, AK ;
Raisman, G ;
Silver, J .
NATURE, 1997, 390 (6661) :680-683
[5]   Sciatic nerve regeneration in rats induced by transplantation of in vitro differentiated bone-marrow stromal cells [J].
Dezawa, M ;
Takahashi, I ;
Esaki, M ;
Takano, M ;
Sawada, H .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2001, 14 (11) :1771-1776
[6]   Migration and differentiation of neural progenitor cells from two different regions of embryonic central nervous system after transplantation into the intact spinal cord [J].
Enomoto, M ;
Shinomiya, K ;
Okabe, S .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2003, 17 (06) :1223-1232
[7]   SURVIVAL AND DIFFERENTIATION OF ADULT NEURONAL PROGENITOR CELLS TRANSPLANTED TO THE ADULT BRAIN [J].
GAGE, FH ;
COATES, PW ;
PALMER, TD ;
KUHN, HG ;
FISHER, LJ ;
SUHONEN, JO ;
PETERSON, DA ;
SUHR, ST ;
RAY, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (25) :11879-11883
[8]   Nogo-66 receptor antagonist peptide promotes axonal regeneration [J].
GrandPré, T ;
Li, SX ;
Strittmatter, SM .
NATURE, 2002, 417 (6888) :547-551
[9]   Marrow stromal cells form guiding strands in the injured spinal cord and promote recovery [J].
Hofstetter, CP ;
Schwarz, EJ ;
Hess, D ;
Widenfalk, J ;
El Manira, A ;
Prockop, DJ ;
Olson, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (04) :2199-2204
[10]   Spontaneous regeneration of the pyramidal tract after transection in young rats [J].
Inoue, T ;
Kawaguchi, S ;
Kurisu, K .
NEUROSCIENCE LETTERS, 1998, 247 (2-3) :151-154