Spinal cord injury: Emerging beneficial role of reactive astrocytes' migration

被引:91
作者
Renault-Mihara, Francois [1 ,2 ]
Okada, Seiji [1 ,3 ]
Shibata, Shinsuke [1 ]
Nakamura, Masaya [2 ]
Toyama, Yoshiaki [2 ]
Okano, Hideyuki [1 ]
机构
[1] Keio Univ, Sch Med, Dept Physiol, Shinjuku Ku, Tokyo 1608582, Japan
[2] Keio Univ, Sch Med, Dept Orthoped Surg, Tokyo 1608582, Japan
[3] Kyushu Univ, Grad Sch Med Sci, SSP Stem Cell Unit, Higashi Ku, Fukuoka 8128582, Japan
关键词
spinal cord injury; reactive astrocyte; migration; therapeutic;
D O I
10.1016/j.biocel.2008.03.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Spinal cord injury (SCI), despite considerable progress in palliative care, has currently no satisfying therapeutic leading to functional recovery. Inability of central nervous system severed axons to regenerate after injury is considered to originate from both limited intrinsic capabilities of neurons and inhibitory effect of the local environment. Precisely, the so-called "glial scar" formed by reactive astrocytes in response to injury exerts a well-known axon-outgrowth inhibitory effect. However, recent studies revealed that role of reactive astrocytes after SCI is more complex. During the first weeks after injury, reactive astrocytes indeed protect the tissue and contribute to a spontaneous relative functional recovery. Compaction of the lesion center and seclusion of inflammatory cells by migrating reactive astrocytes seem to underlie this beneficial effect. Stimulation of reactive astrocytes migration in the sub-acute phase of SCI might thus represent a new approach to improve the functional outcome of patients. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1649 / 1653
页数:5
相关论文
共 18 条
[1]  
Bundesen LQ, 2003, J NEUROSCI, V23, P7789
[2]   Functional axonal regeneration through astrocytic scar genetically modified to digest chondroitin sulfate proteoglycans [J].
Cafferty, William B. J. ;
Yang, Shih-Hung ;
Duffy, Philip J. ;
Li, Shuxin ;
Strittmatter, Stephen M. .
JOURNAL OF NEUROSCIENCE, 2007, 27 (09) :2176-2185
[3]  
Cajal SRY., 1928, DEGENERATION REGENER, DOI [10.1093/acprof:oso/9780195065169.001.0001, DOI 10.1093/ACPROF:OSO/9780195065169.001.0001]
[4]   AXONAL ELONGATION INTO PERIPHERAL NERVOUS-SYSTEM BRIDGES AFTER CENTRAL NERVOUS-SYSTEM INJURY IN ADULT-RATS [J].
DAVID, S ;
AGUAYO, AJ .
SCIENCE, 1981, 214 (4523) :931-933
[5]   Reactive astrocytes protect tissue and preserve function after spinal cord injury [J].
Faulkner, JR ;
Herrmann, JE ;
Woo, MJ ;
Tansey, KE ;
Doan, NB ;
Sofroniew, MV .
JOURNAL OF NEUROSCIENCE, 2004, 24 (09) :2143-2155
[6]   Slit and glypican-1 mRNAs are coexpressed in the reactive astrocytes of the injured adult brain [J].
Hagino, S ;
Iseki, K ;
Mori, T ;
Zhang, YX ;
Hikake, T ;
Yokoya, S ;
Takeuchi, M ;
Hasimoto, H ;
Kikuchi, S ;
Wanaka, A .
GLIA, 2003, 42 (02) :130-138
[7]   Astrocytic control of glutamatergic activity: astrocytes as stars of the show [J].
Hertz, L ;
Zielke, HR .
TRENDS IN NEUROSCIENCES, 2004, 27 (12) :735-743
[8]   Chondroitinase ABC combined with neural stem progenitor cell transplantation enhances graft cell migration and outgrowth of growth-associated protein-43-positive fibers after rat spinal cord injury [J].
Ikegami, T ;
Nakamura, M ;
Yamane, J ;
Katoh, H ;
Okada, S ;
Iwanami, A ;
Watanabe, K ;
Ishii, K ;
Kato, F ;
Fujita, H ;
Takahashi, T ;
Okano, HJ ;
Toyama, Y ;
Okano, H .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2005, 22 (12) :3036-3046
[9]   A demographic profile of new traumatic spinal cord injuries: Change and stability over 30 years [J].
Jackson, AB ;
Dijkers, M ;
DeVivo, MJ ;
Poczatek, RB .
ARCHIVES OF PHYSICAL MEDICINE AND REHABILITATION, 2004, 85 (11) :1740-1748
[10]   REGENERATION IN THE VERTEBRATE CENTRAL-NERVOUS-SYSTEM - PHYLOGENY, ONTOGENY, AND MECHANISMS [J].
LARNER, AJ ;
JOHNSON, AR ;
KEYNES, RJ .
BIOLOGICAL REVIEWS OF THE CAMBRIDGE PHILOSOPHICAL SOCIETY, 1995, 70 (04) :597-619