Neural stem cells protect against glutamate-induced excitotoxicity and promote survival of injured motor neurons through the secretion of neurotrophic factors

被引:178
作者
Lladó, J
Haenggeli, C
Maragakis, NJ
Snyder, EY
Rothstein, JD
机构
[1] Johns Hopkins Univ, Dept Neurol & Neurosci, Baltimore, MD 21287 USA
[2] Burnham Inst, La Jolla, CA 92037 USA
[3] Harvard Univ, Sch Med, Dept Neurol, Boston, MA 02114 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.mcn.2004.07.010
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Besides their capacity to give rise to neurons and/or glia, neural stem cells (NSCs) appear to inherently secrete neurotrophic factors beneficial to injured neurons. To test this potential, we have implanted NSCs onto or adjacent to spinal cord cultures. When NSCs were placed adjacent to the spinal cord sections, motor neuron axons grew toward the NSCs. Furthermore, conditioned medium from NSCs cultures was also able to induce similar axonal outgrowth, suggesting that these NSCs secrete soluble factors that have tropic and/or trophic properties. ELISA revealed that the NSCs secrete glial cell-line-derived factor (GDNF) and nerve growth factor (NGF). Interestingly, preincubation of the conditioned medium with GDNF-blocking antibodies abolished axonal outgrowth. We also showed that NSCs can protect spinal cord cultures from experimentally induced excitotoxic damage. The neuroprotective potential of NSCs was further confirmed in vivo by their ability to protect against motor neuron cell death. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:322 / 331
页数:10
相关论文
共 43 条
  • [1] Neural stem cells display extensive tropism for pathology in adult brain: Evidence from intracranial gliomas
    Aboody, KS
    Brown, A
    Rainov, NG
    Bower, KA
    Liu, SX
    Yang, W
    Small, JE
    Herrlinger, U
    Ourednik, V
    Black, PM
    Breakefield, XO
    Snyder, EY
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (23) : 12846 - 12851
  • [2] The GDNF family: Signalling, biological functions and therapeutic value
    Airaksinen, MS
    Saarma, M
    [J]. NATURE REVIEWS NEUROSCIENCE, 2002, 3 (05) : 383 - 394
  • [3] Neuroprotection through delivery of glial cell line-derived neurotrophic factor by neural stem cells in a mouse model of Parkinson's disease
    Åkerud, P
    Canals, JM
    Snyder, EY
    Arenas, E
    [J]. JOURNAL OF NEUROSCIENCE, 2001, 21 (20) : 8108 - 8118
  • [4] Glial cell line-derived neurotrophic factor released by synthetic guidance channels promotes facial nerve regeneration in the rat
    Barras, FM
    Pasche, P
    Bouche, N
    Aebischer, P
    Zurn, AD
    [J]. JOURNAL OF NEUROSCIENCE RESEARCH, 2002, 70 (06) : 746 - 755
  • [5] Baumgartner BJ, 1998, J NEUROSCI RES, V54, P766, DOI 10.1002/(SICI)1097-4547(19981215)54:6<766::AID-JNR4>3.0.CO
  • [6] 2-A
  • [7] NEURAL GRAFTING IN ANIMAL-MODELS OF NEURODEGENERATIVE DISEASES
    BJORKLUND, A
    GAGE, FH
    [J]. ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1985, 457 : 53 - 81
  • [8] GDNF gene delivery to injured adult CNS motor neurons promotes axonal growth, expression of the trophic neuropeptide CGRP, and cellular protection
    Blesch, A
    Tuszynski, MH
    [J]. JOURNAL OF COMPARATIVE NEUROLOGY, 2001, 436 (04) : 399 - 410
  • [9] ALS-linked SOD1 mutant G85R mediates damage to astrocytes and promotes rapidly progressive disease with SOD1-containing inclusions
    Bruijn, LI
    Becher, MW
    Lee, MK
    Anderson, KL
    Jenkins, NA
    Copeland, NG
    Sisodia, SS
    Rothstein, JD
    Borchelt, DR
    Price, DL
    Cleveland, DW
    [J]. NEURON, 1997, 18 (02) : 327 - 338
  • [10] COCCIA C, 1999, ABSTR SOC NEUROSCI, V25, P425