Therapeutical Strategies for Spinal Cord Injury and a Promising Autologous Astrocyte-Based Therapy Using Efficient Reprogramming Techniques
Molecular Neurobiology, ISSN: 1559-1182, Vol: 53, Issue: 5, Page: 2826-2842
2016
- 21Citations
- 73Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations21
- Citation Indexes21
- 21
- CrossRef16
- Captures73
- Readers73
- 73
Review Description
Spinal cord injury (SCI) is a traumatic event resulting in disturbances to normal sensory, motor, or autonomic functions, which ultimately impacts a patient’s physical, psychological, and social well-being. Until now, no available therapy for SCI can effectively slow down or halt the disease progression. Compared to traditional treatments, e.g., medication, surgery, and functional electrical stimulation, stem cell replacement therapy shows high potential for repair and functional plasticity. Thus, stem cell therapy may provide a promising strategy in curative treatment of SCI, specifically when considering the requirement of neuron replenishment in the spinal cord after distinct acute injuries. However, the therapeutic application of neural stem cells (NSCs) still faces enormous challenges, such as ethical issues, possible inflammatory reactions, graft rejection, and tumor formation. Therefore, it is of vital interest to identify more suitable sources of cells with stem cell potential, which might potentially be harnessed for local neural repair. Due to abovementioned possible drawbacks, these cells should be autologous. Reprogramming of astrocytes to generate the desired neuronal cell types would open the door to autologous cell transplantation and treatment of SCI without possible severe side effects. In this paper, we review the relevant therapeutic strategies for SCI, and conversion of astrocyte into NSCs, suggesting this procedure as a possible treatment option.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84927553692&origin=inward; http://dx.doi.org/10.1007/s12035-015-9157-7; http://www.ncbi.nlm.nih.gov/pubmed/25863960; http://link.springer.com/10.1007/s12035-015-9157-7; https://dx.doi.org/10.1007/s12035-015-9157-7; https://link.springer.com/article/10.1007/s12035-015-9157-7; http://link.springer.com/content/pdf/10.1007/s12035-015-9157-7.pdf; https://link.springer.com/content/pdf/10.1007/s12035-015-9157-7.pdf; https://link.springer.com/content/pdf/10.1007%2Fs12035-015-9157-7.pdf; http://link.springer.com/article/10.1007/s12035-015-9157-7/fulltext.html; http://link.springer.com/article/10.1007%2Fs12035-015-9157-7; http://link.springer.com/content/pdf/10.1007/s12035-015-9157-7
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