Cellular repair of CNS disorders: an immunological perspective

被引:48
作者
Chen, Zhiguo [1 ]
Palmer, Theo D. [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Neurosurg, Stanford, CA 94305 USA
关键词
D O I
10.1093/hmg/ddn104
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
Cellular repair is a promising strategy for treating central nervous system (CNS) disorders. Several strategies have been contemplated including replacement of neurons or glia that have been lost due to injury or disease, use of cellular grafts to modify or augment the functions of remaining neurons and/or use of cellular grafts to protect neural tissue by local delivery of growth or trophic factors. Depending on the specific disease target, there may be one or many cell types that could be considered for therapy. In each case, an additional variable must be considered-the role of the immune system in both the injury process itself and in the response to incoming cells. Cellular transplants can be roughly categorized into autografts, allografts and xenografts. Despite the immunological privilege of the CNS, allografts and xenografts can elicit activation of the innate and adaptive immune system. In this article, we evaluate the various effects that immune cells and signals may have on the survival, proliferation, differentiation and migration/integration of transplanted cells in therapeutic approaches to CNS injury and disease.
引用
收藏
页码:R84 / R92
页数:9
相关论文
共 73 条
[1]   Neuronal damage in autoimmune neuroinflammation mediated by the death ligand TRAIL [J].
Aktas, O ;
Smorodchenko, A ;
Brocke, S ;
Infante-Duarte, C ;
Topphoff, US ;
Vogt, J ;
Prozorovski, T ;
Meier, S ;
Osmanova, V ;
Pohl, E ;
Bechmann, I ;
Nitsch, R ;
Zipp, F .
NEURON, 2005, 46 (03) :421-432
[2]   Human neural progenitors deliver glial cell line-derived neurotrophic factor to parkinsonian rodents and aged primates [J].
Behrstock, S ;
Ebert, A ;
McHugh, J ;
Vosberg, S ;
Moore, J ;
Schneider, B ;
Capowski, E ;
Hei, D ;
Kordower, J ;
Aebischer, P ;
Svendsen, CN .
GENE THERAPY, 2006, 13 (05) :379-388
[3]   Skin-derived precursors generate myelinating Schwann cells that promote remyelination and functional recovery after contusion spinal cord injury [J].
Biernaskie, Jeff ;
Sparling, Joseph S. ;
Liu, Jie ;
Shannon, Casey P. ;
Plemel, Jason R. ;
Xie, Yuanyun ;
Miller, Freda D. ;
Tetzlaff, Wolfram .
JOURNAL OF NEUROSCIENCE, 2007, 27 (36) :9545-9559
[4]   Neural transplantation for the treatment of Parkinson's disease [J].
Björklund, A ;
Dunnett, SB ;
Brundin, P ;
Stoessl, AJ ;
Freed, CR ;
Breeze, RE ;
Levivier, M ;
Peschanski, M ;
Studer, L ;
Barker, R .
LANCET NEUROLOGY, 2003, 2 (07) :437-445
[5]   Embryonic stem cells develop into functional dopaminergic neurons after transplantation in a Parkinson rat model [J].
Björklund, LM ;
Sánchez-Pernaute, R ;
Chung, SM ;
Andersson, T ;
Chen, IYC ;
McNaught, KS ;
Brownell, AL ;
Jenkins, BG ;
Wahlestedt, C ;
Kim, KS ;
Isacson, O .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (04) :2344-2349
[6]   Immature and neurally differentiated mouse embryonic stem cells do not express a functional Fas/Fas ligand system [J].
Brunlid, Gabriella ;
Pruszak, Jan ;
Holmes, Benjamin ;
Isacson, Ole ;
Sonntag, Kai-Christian .
STEM CELLS, 2007, 25 (10) :2551-2558
[7]   Chronically increased transforming growth factor-β1 strongly inhibits hippocampal neurogenesis in aged mice [J].
Buckwalter, Marion S. ;
Yamane, Makiko ;
Coleman, Bronwen S. ;
Ormerod, Brandi K. ;
Chin, Jocelyn T. ;
Palmer, Theo ;
Wyss-Coray, Tony .
AMERICAN JOURNAL OF PATHOLOGY, 2006, 169 (01) :154-164
[8]   Induction and blockage of oligodendrogenesis by differently activated microglia in an animal model of multiple sclerosis [J].
Butovsky, O ;
Landa, G ;
Kunis, G ;
Ziv, Y ;
Avidan, H ;
Greenberg, N ;
Schwartz, A ;
Smirnov, I ;
Pollack, A ;
Jung, S ;
Schwartz, M .
JOURNAL OF CLINICAL INVESTIGATION, 2006, 116 (04) :905-915
[9]   Microglia activated by IL-4 or IFN-γ differentially induce neurogenesis and oligodendrogenesis from adult stem/progenitor cells [J].
Butovsky, O ;
Ziv, Y ;
Schwartz, A ;
Landa, G ;
Talpalar, AE ;
Pluchino, S ;
Martino, G ;
Schwartz, M .
MOLECULAR AND CELLULAR NEUROSCIENCE, 2006, 31 (01) :149-160
[10]   Producing primate embryonic stem cells by somatic cell nuclear transfer [J].
Byrne, J. A. ;
Pedersen, D. A. ;
Clepper, L. L. ;
Nelson, M. ;
Sanger, W. G. ;
Gokhale, S. ;
Wolf, D. P. ;
Mitalipov, S. M. .
NATURE, 2007, 450 (7169) :497-U3