Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2015 Jan 20:8:454.
doi: 10.3389/fnins.2014.00454. eCollection 2014.

Activation of endogenous neural stem cells for multiple sclerosis therapy

Affiliations

Activation of endogenous neural stem cells for multiple sclerosis therapy

Iliana Michailidou et al. Front Neurosci. .

Abstract

Multiple sclerosis (MS) is a chronic inflammatory disorder of the central nervous system, leading to severe neurological deficits. Current MS treatment regimens, consist of immunomodulatory agents aiming to reduce the rate of relapses. However, these agents are usually insufficient to treat chronic neurological disability. A promising perspective for future therapy of MS is the regeneration of lesions with replacement of the damaged oligodendrocytes or neurons. Therapies targeting to the enhancement of endogenous remyelination, aim to promote the activation of either the parenchymal oligodendrocyte progenitor cells or the subventricular zone-derived neural stem cells (NSCs). Less studied but highly potent, is the strategy of neuronal regeneration with endogenous NSCs that although being linked to numerous limitations, is anticipated to ameliorate cognitive disability in MS. Focusing on the forebrain, this review highlights the role of NSCs in the regeneration of MS lesions.

Keywords: gliogenesis; multiple sclerosis; neural stem cells; neurogenesis; therapy.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Model strategy for regeneration of MS lesions via activation of adult SVZ-derived NSCs. Stimulation of neural stem cells (NSCs) via intracerebroventricular administration of, e.g., growth factors may lead to the regeneration of newly formed lesions which are located in white matter (WM) or gray matter (GM) areas nearby the subventricular zone (SVZ) of the multiple sclerosis (MS) brain (A) such as the adjacent corpus callosum (CC) (B) and the cingulate gyrus (C).

Similar articles

Cited by

References

    1. Aloe L., Micera A. (1998). A role of nerve growth factor in oligodendrocyte growth and differentiation of EAE affected rats. Arch. Ital. Biol. 136, 247–256. - PubMed
    1. Andersson P. B., Waubant E., Gee L., Goodkin D. E. (1999). Multiple sclerosis that is progressive from the time of onset: clinical characteristics and progression of disability. Arch. Neurol. 56, 1138–1142. 10.1001/archneur.56.9.1138 - DOI - PubMed
    1. Armstrong R. C., Le T. Q., Frost E. E., Borke R. C., Vana A. C. (2002). Absence of fibroblast growth factor 2 promotes oligodendroglial repopulation of demyelinated white matter. J. Neurosci. Off. J. Soc. Neurosci. 22, 8574–8585. - PMC - PubMed
    1. Baer A. S., Syed Y. A., Kang S. U., Mitteregger D., Vig R., Ffrench-Constant C., et al. . (2009). Myelin-mediated inhibition of oligodendrocyte precursor differentiation can be overcome by pharmacological modulation of Fyn-RhoA and protein kinase C signalling. Brain J. Neurol. 132, 465–481. 10.1093/brain/awn334 - DOI - PMC - PubMed
    1. Barak Y., Achiron A. (2002). Effect of interferon-beta-1b on cognitive functions in multiple sclerosis. Eur. Neurol. 47, 11–14. 10.1159/000047940 - DOI - PubMed

LinkOut - more resources