Document Type
Journal Article
Publication Date
11-2014
Journal
GLIA
Volume
Volume 62, Issue 11
Inclusive Pages
1905-1915
Abstract
Amongst neurological diseases, multiple sclerosis (MS) presents an attractive target for regenerative medicine. This is because the primary pathology, the loss of myelin-forming oligodendrocytes, can be followed by a spontaneous and efficient regenerative process called remyelination. While cell transplantation approaches have been explored as a means of replacing lost oligodendrocytes, more recently therapeutic approaches that target the endogenous regenerative process have been favored. This is in large part due to our increasing understanding of (1) the cell types within the adult brain that are able to generate new oligodendrocytes, (2) the mechanisms and pathways by which this achieved, and (3) an emerging awareness of the reasons why remyelination efficiency eventually fails. Here we review some of these advances and also highlight areas where questions remain to be answered in both the biology and translational potential of this important regenerative process. GLIA 2014;62:1905–1915
Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.
APA Citation
Franklin, R.J.M., Gallo, V. (2014). The translational biology of remyelination: Past, present, and future. GLIA, 62(11), 1905-1915.
Peer Reviewed
1
Open Access
1
Comments
Reproduced with permission of Wiley Periodicals, Inc. GLIA.