Transplant therapy: Recovery of function after spinal cord injury

被引:50
作者
Zompa, EA
Cain, LD
Everhart, AW
Moyer, MP
Hulsebosch, CE
机构
[1] UNIV TEXAS, MED BRANCH, DEPT ANAT & NEUROSCI, GALVESTON, TX 77555 USA
[2] UNIV TEXAS, HLTH SCI CTR, DEPT SURG, SAN ANTONIO, TX 78284 USA
关键词
spinal cord injury; transplants; human fetal tissue; human fetal spinal cord cells; behavior; human progenitor cells; CNS; review;
D O I
10.1089/neu.1997.14.479
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Spinal cord injuries (SCI) result in devastating loss of function and altered sensation. Presently, victims of SCI have few remedies for the loss of motor function and the altered sensation often experienced subsequent to the injury. A goal in SCI research is to improve function in both acute and chronic injuries. Among the most successful interventions is the utilization of transplanted tissues toward improved recovery. The theory is that the transplanted tissue could (1) bridge the spinal lesion and provide chemical and/or mechanical guidance for host neurons to grow across the lesion, (2) bridge the spinal lesion and provide additional cellular elements to repair the damaged circuitry, (3) provide factors that would rescue neurons that would otherwise die and/or modulate neural circuits to improve function. A variety of tissues and cells have been added to the adult mammalian spinal cord to encourage restoration of function. These include Schwann cells, motor neurons, dorsal root ganglia, adrenal tissue, hybridomas, peripheral nerves, and fetal spinal cord (FSC) tissue en bloc or as disassociated cells. It is postulated that these tissues would rescue or replace injured adult neurons, which would then integrate or promote the regeneration of the spinal cord circuitry and restore function. In some instances, host-appropriate circuitry is supplied by the transplant and functional improvement is demonstrated. In this presentation, specific examples of recent work with transplanted tissue and cells that demonstrate improved behavioral outcome are presented. New recent work describing the in vitro propagation and characterization of human fetal spinal cord multipotential progenitor cells are also described in the context of a potential resource for transplantable cells. Additionally, data from transplantation experiments of human FSC cells into nonimmunosuppressed rat spinal cord are described, and the resultant improvements in behavioral outcome reported. Lastly, directions for future SCI research are proposed.
引用
收藏
页码:479 / 506
页数:28
相关论文
共 159 条
[1]  
Aguayo A.J., 1985, SYNAPTIC PLASTICITY, P457
[2]   DEVELOPMENTAL APPEARANCE, ANTIGENIC PROFILE, AND PROLIFERATION OF GLIAL-CELLS OF THE HUMAN EMBRYONIC SPINAL-CORD - AN IMMUNOCYTOCHEMICAL STUDY USING DISSOCIATED CULTURED-CELLS [J].
ALOISI, F ;
GIAMPAOLO, A ;
RUSSO, G ;
PESCHLE, C ;
LEVI, G .
GLIA, 1992, 5 (03) :171-181
[3]   FETAL NEURAL GRAFTS AND REPAIR OF THE INJURED SPINAL-CORD [J].
ANDERSON, DK ;
HOWLAND, DR ;
REIER, PJ .
BRAIN PATHOLOGY, 1995, 5 (04) :451-457
[4]   CELLULAR EVENTS ASSOCIATED WITH PERIPHERALLY INDUCED REJECTION OF MATURE NEURAL XENOGRAFTS PLACED INTO NEONATAL RAT BRAINS [J].
BACKES, MG ;
LUND, RD ;
LAGENAUR, CF ;
KUNZ, HW ;
GILL, TJ .
JOURNAL OF COMPARATIVE NEUROLOGY, 1990, 295 (03) :428-437
[5]   RECOVERY OF LOCOMOTION AFTER CHRONIC SPINALIZATION IN THE ADULT CAT [J].
BARBEAU, H ;
ROSSIGNOL, S .
BRAIN RESEARCH, 1987, 412 (01) :84-95
[6]   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
[7]  
Berkowitz M, 1992, EC CONSEQUENCES TRAU
[8]   DENDRITIC ALTERATION OF RAT SPINAL MOTONEURONS AFTER DORSAL HORN MINCE - COMPUTER RECONSTRUCTION OF DENDRITIC FIELDS [J].
BERNSTEIN, JJ ;
STANDLER, NA .
EXPERIMENTAL NEUROLOGY, 1983, 82 (03) :532-540
[9]   SPINAL MOTONEURON DENDRITIC ALTERATION AFTER SPINAL-CORD HEMISECTION IN THE RAT [J].
BERNSTEIN, JJ ;
WACKER, W ;
STANDLER, N .
EXPERIMENTAL NEUROLOGY, 1984, 83 (03) :548-554
[10]  
BJORKLUND A, 1983, ACTA PHYSIOL SCAND, P9