Authors
Malgorzata Zawadzka, Leanne E Rivers, Stephen PJ Fancy, Chao Zhao, Richa Tripathi, Francoise Jamen, Kaylene Young, Alexander Goncharevich, Hartmut Pohl, Matteo Rizzi, David H Rowitch, Nicoletta Kessaris, Ueli Suter, William D Richardson, Robin JM Franklin
Publication date
2010/6/4
Journal
Cell stem cell
Volume
6
Issue
6
Pages
578-590
Publisher
Elsevier
Description
After central nervous system (CNS) demyelination—such as occurs during multiple sclerosis—there is often spontaneous regeneration of myelin sheaths, mainly by oligodendrocytes but also by Schwann cells. The origins of the remyelinating cells have not previously been established. We have used Cre-lox fate mapping in transgenic mice to show that PDGFRA/NG2-expressing glia, a distributed population of stem/progenitor cells in the adult CNS, produce the remyelinating oligodendrocytes and almost all of the Schwann cells in chemically induced demyelinated lesions. In contrast, the great majority of reactive astrocytes in the vicinity of the lesions are derived from preexisting FGFR3-expressing cells, likely to be astrocytes. These data resolve a long-running debate about the origins of the main players in CNS remyelination and reveal a surprising capacity of CNS precursors to generate Schwann cells, which …
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