Why does the central nervous system not regenerate after injury?

被引:20
作者
Nicholls, JG [1 ]
Adams, WB [1 ]
Eugenin, J [1 ]
Geiser, R [1 ]
Lepre, M [1 ]
Luque, JM [1 ]
Wintzer, M [1 ]
机构
[1] Univ Basel, Biozentrum, Dept Pharmacol, Basel, Switzerland
关键词
injury; Monodelphis domestica; neuroglia; opossum; spinal cord;
D O I
10.1016/S0039-6257(99)00008-9
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Spinal cord injuries in humans and in other mammals ale never followed by regrowth. In recent years, considerable progress has been made in analyzing mechanisms that promote and inhibit regeneration. The focus of this review is changes that occur in the transition period in development when the central nervous system (CNS) changes from being able to regenerate to the adult state of failure. In our experiments we have used the neonatal opossum (Monodelphis domestica), which corresponds to a 14-day embryonic rat or mouse. The CNS isolated from an opossum pup and maintained in culture shows dramatic regeneration. Fibers grow through and beyond lesions and reform synaptic connections with their targets. Similarly, anesthetized neonatal. pups attached to tilt: mother recover the ability to walk after complete spinal cord transection. Although the CNS isolated from a 9-day-old animal will regenerate in vitro, CNS from a 12-day-old will not. This is the stage wt which glial cells in the CNS develop. Present research is devoted toward molecular screening to determine which growth-promoting molecules decrease during development, which inhibitory molecules increase, and which receptors on growing axons become altered. Despite progress in many laboratories, major hurdles must be overcome before patients can hope to be treated. Nevertheless, the picture today is not as discouraging as it was: one can think of strategies for research on spinal cord injury so as to promote regeneration and restore function. (C) 1999 by Elsevier Science Inc. All rights reserved.
引用
收藏
页码:S136 / S141
页数:6
相关论文
共 22 条
[1]   DEGENERATIVE AND REGENERATIVE RESPONSES OF INJURED NEURONS IN THE CENTRAL-NERVOUS-SYSTEM OF ADULT MAMMALS [J].
AGUAYO, AJ ;
RASMINSKY, M ;
BRAY, GM ;
CARBONETTO, S ;
MCKERRACHER, L ;
VILLEGASPEREZ, MP ;
VIDALSANZ, M ;
CARTER, DA .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 1991, 331 (1261) :337-343
[2]   Spinal cord repair in adult paraplegic rats: Partial restoration of hind limb function [J].
Cheng, H ;
Cao, YH ;
Olson, L .
SCIENCE, 1996, 273 (5274) :510-513
[3]   CHARACTERIZATION OF THE SPROUTING RESPONSE OF AXON-LIKE PROCESSES FROM RETINAL GANGLION-CELLS AFTER AXOTOMY IN ADULT HAMSTERS - A MODEL USING INTRAVITREAL IMPLANTATION OF A PERIPHERAL-NERVE [J].
CHO, EYP ;
SO, KF .
JOURNAL OF NEUROCYTOLOGY, 1992, 21 (08) :589-603
[4]   Restoration of dopamine transporter density in the striatum of fetal ventral mesencephalon-grafted, but not sham-grafted, MPTP-treated Parkinsonian monkeys [J].
Elsworth, JD ;
Brittan, MS ;
Taylor, JR ;
Sladek, JR ;
AlTikriti, MS ;
ZeaPonce, Y ;
Innis, RB ;
Redmond, DE ;
Roth, RH .
CELL TRANSPLANTATION, 1996, 5 (02) :315-325
[5]  
HASAN SJ, 1993, J NEUROSCI, V13, P492
[6]   RESTORATION OF FUNCTION BY REPLACEMENT OF SPINAL-CORD SEGMENTS IN THE RAT [J].
IWASHITA, Y ;
KAWAGUCHI, S ;
MURATA, M .
NATURE, 1994, 367 (6459) :167-170
[7]   Repair of adult rat corticospinal tract by transplants of olfactory ensheathing cells [J].
Li, Y ;
Field, PM ;
Raisman, G .
SCIENCE, 1997, 277 (5334) :2000-2002
[8]  
Luque JM, 1998, J COMP NEUROL, V390, P427, DOI 10.1002/(SICI)1096-9861(19980119)390:3<427::AID-CNE9>3.0.CO
[9]  
2-3
[10]   Chiasmatic specificity in the regenerating mammalian optic nerve [J].
MacLaren, RE ;
Taylor, JSH .
EXPERIMENTAL NEUROLOGY, 1997, 147 (02) :279-286