Schwann cell transplantation for repair of the adult spinal cord

被引:182
作者
Oudega, M
Xu, XM
机构
[1] Johns Hopkins Univ, Sch Med, Dept Neurol, Kennedy Krieger Inst,Int Ctr Spinal Cord Injury, Baltimore, MD 21205 USA
[2] Univ Miami, Sch Med, Miami Project Cure Paralysis, Miami, FL 33152 USA
[3] Univ Miami, Sch Med, Dept Neurol Surg, Miami, FL 33152 USA
[4] Univ Louisville, Kentucky Spinal Cord Injury Res Ctr, Dept Neurol Surg, Sch Med, Louisville, KY 40292 USA
[5] Univ Louisville, Kentucky Spinal Cord Injury Res Ctr, Dept Anat Sci & Neurobiol, Sch Med, Louisville, KY 40292 USA
关键词
cAMP; central nervous system; endogenous repair; glial scar; neurotrophins; olfactory ensheathing glia; peripheral nerve; Schwann cell culture; spinal cord injury;
D O I
10.1089/neu.2006.23.453
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
The Schwann cell is one of the most widely studied cell types for repair of the spinal cord. These cells play a crucial role in endogenous repair of peripheral nerves due to their ability to dedifferentiate, migrate, proliferate, express growth promoting factors, and myelinate regenerating axons. Following trauma to the spinal cord, Schwann cells migrate from the periphery into the injury site, where they apparently participate in endogenous repair processes. For transplantation into the spinal cord, large numbers of Schwann cells are necessary to fill injury-induced cystic cavities. Several culture systems have been developed that provide large, highly purified populations of Schwann cells. Importantly, the development of in vitro systems to harvest human Schwann cells presents a unique opportunity for autologous transplantation in the clinic. In animal models of spinal cord injury (SCI), grafting Schwann cells or peripheral nerve into the lesion site has been shown to promote axonal regeneration and myelination. However, axons do not regenerate beyond the transplant due to the inhibitory nature of the glial scar surrounding the injury. To overcome the glial scar inhibition, additional approaches such as increasing the intrinsic capacity of axons to regenerate and/or removal of the inhibitory molecules associated with reactive astrocytes and/or oligodendrocyte myelin should be incorporated. Clearly, Schwann cells have great potential for repair of the injured spinal cord, but they need to be combined with other interventions to maximize axonal regeneration and functional recovery.
引用
收藏
页码:453 / 467
页数:15
相关论文
共 124 条
[1]   DETECTION OF BRAIN-DERIVED NEUROTROPHIC FACTOR-LIKE ACTIVITY IN FIBROBLASTS AND SCHWANN-CELLS - INHIBITION BY ANTIBODIES TO NGF [J].
ACHESON, A ;
BARKER, PA ;
ALDERSON, RF ;
MILLER, FD ;
MURPHY, RA .
NEURON, 1991, 7 (02) :265-275
[2]   MULTIPOTENTIALITY OF SCHWANN-CELLS IN CROSS-ANASTOMOSED AND GRAFTED MYELINATED AND UNMYELINATED NERVES - QUANTITATIVE MICROSCOPY AND AUTORADIOGRAPHY [J].
AGUAYO, AJ ;
EPPS, J ;
CHARRON, L ;
BRAY, GM .
BRAIN RESEARCH, 1976, 104 (01) :1-20
[3]   NODE OF RANVIER IN EXPERIMENTAL ALLERGIC NEURITIS - ELECTRON-MICROSCOPE STUDY [J].
ALLT, G .
JOURNAL OF NEUROCYTOLOGY, 1975, 4 (01) :63-76
[4]   COMPARISON OF THE SCHWANN-CELL SURFACE AND SCHWANN-CELL EXTRACELLULAR-MATRIX AS PROMOTERS OF NEURITE GROWTH [J].
ARD, MD ;
BUNGE, RP ;
BUNGE, MB .
JOURNAL OF NEUROCYTOLOGY, 1987, 16 (04) :539-555
[5]   NEUROTROPHIN-3 PREVENTS THE DEATH OF ADULT CENTRAL NORADRENERGIC NEURONS IN-VIVO [J].
ARENAS, E ;
PERSSON, H .
NATURE, 1994, 367 (6461) :368-371
[6]   HUMAN SCHWANN-CELLS IN TISSUE-CULTURE - HISTOCHEMICAL AND ULTRASTRUCTURAL STUDIES [J].
ASKANAS, V ;
ENGEL, WK ;
DALAKAS, MC ;
LAWRENCE, JV ;
CARTER, LS .
ARCHIVES OF NEUROLOGY, 1980, 37 (06) :329-337
[7]   MACROPHAGE-MEDIATED MYELIN-RELATED MITOGENIC FACTOR FOR CULTURED SCHWANN-CELLS [J].
BAICHWAL, RR ;
BIGBEE, JW ;
DEVRIES, GH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (05) :1701-1705
[8]   Neurotrophins BDNF and NT-3 promote axonal re-entry into the distal host spinal cord through Schwann cell-seeded mini-channels [J].
Bamber, NI ;
Li, HY ;
Lu, XB ;
Oudega, M ;
Aebischer, P ;
Xu, XM .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2001, 13 (02) :257-268
[9]   Olfactory ensheathing cells: Unique glial cell types? [J].
Barnett, SC .
JOURNAL OF NEUROTRAUMA, 2004, 21 (04) :375-382
[10]   GENETIC-LINKAGE AND MENTAL-DISORDERS - AN UPDATE ON ANALYTIC METHODOLOGIES [J].
BARON, M .
BIOLOGICAL PSYCHIATRY, 1994, 36 (01) :1-4