Accumulation of the inhibitory receptor EphA4 may prevent regeneration of corticospinal tract axons following lesion

被引:70
作者
Fabes, J
Anderson, P
Yáñez-Muñoz, RJ
Thrasher, A
Brennan, C
Bolsover, S
机构
[1] UCL, Dept Physiol, London WC1E 6BT, England
[2] UCL, Dept Anat, London WC1E 6BT, England
[3] Queen Mary Univ London, St Bartholmews & London Sch Med & Dent, Inst Canc, Dept Med Oncol, London EC1M 6BQ, England
[4] Inst Child Hlth, Mol Immunol Unit, London WC1N 1EH, England
[5] Univ London Queen Mary Coll, Sch Biol Sci, London E1 4NS, England
关键词
axonal regeneration; ephrins; rat; spinal cord injury;
D O I
10.1111/j.1460-9568.2006.04704.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We have examined the expression of Eph receptors and their ephrin ligands in adult rat spinal cord before and after lesion. Neurons in adult motor cortex express EphA4 mRNA, but the protein is undetectable in uninjured corticospinal tract. In contrast, after dorsal column hemisection EphA4 protein accumulates in proximal axon stumps. One of the ligands for EphA4, ephrinB2, is normally present in the grey matter flanking the corticospinal tract but after injury is markedly up-regulated in astrocytes in the glial scar. The result is that, after a lesion, corticospinal tract axons bear high levels of EphA4 and are surrounded to front and sides by a continuous basket of cognate inhibitory ephrin ligand. We suggest that a combination of EphA4 accumulation in the injured axons and up-regulation of ephrinB2 in the surrounding astrocytes leads to retraction of corticospinal axons and inhibition of their regeneration in the weeks after a spinal lesion.
引用
收藏
页码:1721 / 1730
页数:10
相关论文
共 44 条
[1]  
BARTSCH S, 1992, J NEUROSCI, V12, P736
[2]   EphB receptors and ephrin-B ligands regulate spinal sensory connectivity and modulate pain processing [J].
Battaglia, AA ;
Sehayek, K ;
Grist, J ;
McMahon, SB ;
Gavazzi, I .
NATURE NEUROSCIENCE, 2003, 6 (04) :339-340
[3]   Ephrin-B3 is a myelin-based inhibitor of neurite outgrowth [J].
Benson, MD ;
Romero, MI ;
Lush, ME ;
Lu, QR ;
Henkemeyer, M ;
Parada, LF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (30) :10694-10699
[4]   Semiquantitative expression analysis of ephrine-receptor tyrosine kinase mRNA's in a rat model of traumatic brain injury [J].
Biervert, C ;
Horvath, E ;
Fahrig, T .
NEUROSCIENCE LETTERS, 2001, 315 (1-2) :25-28
[5]   Chondroitinase ABC promotes functional recovery after spinal cord injury [J].
Bradbury, EJ ;
Moon, LDF ;
Popat, RJ ;
King, VR ;
Bennett, GS ;
Patel, PN ;
Fawcett, JW ;
McMahon, SB .
NATURE, 2002, 416 (6881) :636-640
[6]   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
[7]  
Brösamle C, 2000, J NEUROSCI, V20, P8061
[8]  
Bundesen LQ, 2003, J NEUROSCI, V23, P7789
[9]   Ephrins in reverse, park and drive [J].
Cowan, CA ;
Henkemeyer, M .
TRENDS IN CELL BIOLOGY, 2002, 12 (07) :339-346
[10]   Metalloproteinase increases in the injured rat spinal cord [J].
de Castro, R ;
Burns, CL ;
McAdoo, DJ ;
Romanic, AM .
NEUROREPORT, 2000, 11 (16) :3551-3554