Current status of experimental cell replacement approaches to spinal cord injury

被引:86
作者
Eftekharpour, Eftekhar [1 ,2 ]
Karimi-Abdolrezaee, Soheila [1 ,2 ,4 ]
Fehlings, Michael G. [1 ,2 ,3 ,4 ]
机构
[1] Univ Toronto, Toronto Western Hosp, Dept Neurosurg, Univ Hlth Network,Krembil Neurosci Ctr,Spinal Pro, Toronto, ON M5T 2S8, Canada
[2] Toronto Western Res Inst, Div Genet & Dev, Toronto, ON, Canada
[3] Univ Toronto, Inst Med Sci, Toronto, ON M5S 1A1, Canada
[4] Univ Toronto, Dept Surg, Toronto, ON M5S 1A1, Canada
关键词
axonal regeneration; spinal cord injury; stem cell therapy;
D O I
10.3171/FOC/2008/24/3-4/E18
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Despite advances in medical and surgical care, the current clinical therapies for spinal cord injury (SCI) are largely ineffective. During the last 2 decades, the search for new therapies has been revolutionized by the discovery of stem cells, which has inspired scientists and clinicians to search for a stem cell-based reparative approaches to many diseases, including neurotrauma. In the present study, the authors briefly summarize current knowledge related to the pathophysiology of SCI, including the concepts of primary and secondary injury and the importance of posttraumatic demyelination. Key inhibitory obstacles that impede axonal regeneration include the glial scar and a number of myelin inhibitory molecules including Nogo. Recent advancements in cell replacement therapy as a therapeutic strategy for SCI are summarized. The strategies include the use of pluripotent human stem cells, embryonic stem cells, and a number of adult-derived stem and progenitor cells such as mesenchymal stem cells, Schwann cells, olfactory ensheathing cells, and adult-derived neural precursor cells. Although current strategies to repair the subacutely injured cord appear promising, many obstacles continue to render the treatment of chronic injuries challenging. Nonetheless, the future for stem cell-based reparative strategies for treating SCI appears bright.
引用
收藏
页数:13
相关论文
共 115 条
[1]   DETECTION OF BRAIN-DERIVED NEUROTROPHIC FACTOR-LIKE ACTIVITY IN FIBROBLASTS AND SCHWANN-CELLS - INHIBITION BY ANTIBODIES TO NGF [J].
ACHESON, A ;
BARKER, PA ;
ALDERSON, RF ;
MILLER, FD ;
MURPHY, RA .
NEURON, 1991, 7 (02) :265-275
[2]   Role of L- and N-type calcium channels in the pathophysiology of traumatic spinal cord white matter injury [J].
Agrawal, SK ;
Nashmi, R ;
Fehlings, MG .
NEUROSCIENCE, 2000, 99 (01) :179-188
[3]  
Alvarez-Buylla A, 1998, J NEUROBIOL, V36, P105, DOI 10.1002/(SICI)1097-4695(199808)36:2<105::AID-NEU1>3.0.CO
[4]  
2-5
[5]   Genetic dysmyelination alters the molecular architecture of the nodal region [J].
Arroyo, EJ ;
Xu, T ;
Grinspan, J ;
Lambert, S ;
Levinson, SR ;
Brophy, PJ ;
Peles, E ;
Scherer, SS .
JOURNAL OF NEUROSCIENCE, 2002, 22 (05) :1726-1737
[6]   Update on the treatment of spinal cord injury [J].
Baptiste, Darryl C. ;
Fehlings, Michael G. .
NEUROTRAUMA: NEW INSIGHTS INTO PATHOLOGY AND TREATMENT, 2007, 161 :217-233
[7]   Survival, integration, and axon growth support of glia transplanted into the chronically contused spinal cord [J].
Barakat, DJ ;
Gaglani, SM ;
Neravetla, SR ;
Sanchez, AR ;
Andrade, CM ;
Pressman, Y ;
Puzis, R ;
Garg, MS ;
Bunge, MB ;
Pearse, DD .
CELL TRANSPLANTATION, 2005, 14 (04) :225-240
[8]   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
[9]  
Blits B, 2005, RESTOR NEUROL NEUROS, V23, P313
[10]   Proteomic evaluation reveals that olfactory ensheathing cells but not Schwann cells express calponin [J].
Boyd, JG ;
Jahed, A ;
McDonald, TG ;
Krol, KM ;
Van Eyk, JE ;
Doucette, R ;
Kawaja, MD .
GLIA, 2006, 53 (04) :434-440