Biology Faculty Articles
Document Type
Article
Publication Date
4-26-2014
Publication Title
World Journal of Stem Cells
Keywords
Mesenchymal stem cells, Stem cell therapy, Central nervous system, Retina, Clinical trial
ISSN
1948-0210
Volume
6
Issue/No.
2
First Page
111
Last Page
119
Abstract
Complex circuitry and limited regenerative power make central nervous system (CNS) disorders the most challenging and difficult for functional repair. With elusive disease mechanisms, traditional surgical and medical interventions merely slow down the progression of the neurodegenerative diseases. However, the number of neurons still diminishes in many patients. Recently, stem cell therapy has been proposed as a viable option. Mesenchymal stem cells (MSCs), a widely-studied human adult stem cell population, have been discovered for more than 20 years. MSCs have been found all over the body and can be conveniently obtained from different accessible tissues: bone marrow, blood, and adipose and dental tissue. MSCs have high proliferative and differentiation abilities, providing an inexhaustible source of neurons and glia for cell replacement therapy. Moreover, MSCs also show neuroprotective effects without any genetic modification or reprogramming. In addition, the extraordinary immunomodulatory properties of MSCs enable autologous and heterologous transplantation. These qualities heighten the clinical applicability of MSCs when dealing with the pathologies of CNS disorders. Here, we summarize the latest progress of MSC experimental research as well as human clinical trials for neural and retinal diseases. This review article will focus on multiple sclerosis, spinal cord injury, autism, glaucoma, retinitis pigmentosa and age-related macular degeneration.
Creative Commons License
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License
NSUWorks Citation
Ng, Tsz Kin; Veronica R. Fortino; Daniel Pelaez; and Herman S. Cheung. 2014. "Progress of Mesenchymal Stem Cell Therapy for Neural and Retinal Diseases." World Journal of Stem Cells 6, (2): 111-119. doi:10.4252/wjsc.v6.i2.111.
DOI
10.4252/wjsc.v6.i2.111
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