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PMID: 10811401 Published · ppublish English Journal Article Review

Transplantation options for therapeutic central nervous system remyelination.

Cell transplantation ·Vol. 9 ·No. 2 ·2000-00-00 ·Pages 289-94

Blakemore WF, Franklin RJ

Abstract

Persistent demyelination, in addition to being the major pathology of multiple sclerosis and the leucodystrophies, is also a feature of spinal cord trauma where there is evidence that it contributes to the functional deficit. In experimental animals it is possible to remyelinate demyelinated CNS axons by transplanting cultures containing central or peripheral myelinogenic cells. Using functional testing we have been able to show that transplant-mediated remyelination results in restoration of function lost as a consequence of demyelination. Glial cell transplantation may therefore provide a therapeutic strategy for remyelinating areas of chronic demyelination. This article reviews issues that have to be addressed before glial transplantation can be undertaken in humans. These include: what cells to use, where would the cells come from, and can we predict how much remyelination will be achieved? It concludes that the most promising approach will be to use neural multipotential stem cells isolated from embryonic CNS, expanded in vitro as neurospheres and then committed to oligodendrocyte lineage differentiation prior to implantation. However, even with such preparations, which have considerable myelinating potential, the extent of remyelination that will be achieved cannot currently be predicted with any degree of certainty.

MeSH Terms
Animals Brain Tissue Transplantation Demyelinating Diseases/physiopathology,surgery Fetal Tissue Transplantation Humans Myelin Sheath/physiology Neuroglia/physiology,transplantation Oligodendroglia/transplantation Safety Schwann Cells/transplantation
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Blakemore W F
Department of Clinical Veterinary Medicine, Cambridge, UK.
Franklin R J
Article Info
Journal
Cell transplantation
Abbr.
Cell Transplant
ISSN
0963-6897
Published
2000-00-00
Pages
289-94
Language
English
Region
United States
NLM ID
9208854
Subset
IM
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