4.6 Article

Pre-Existing Mature Oligodendrocytes Do Not Contribute to Remyelination following Toxin-Induced Spinal Cord Demyelination

Journal

AMERICAN JOURNAL OF PATHOLOGY
Volume 186, Issue 3, Pages 511-516

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.ajpath.2015.11.005

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Funding

  1. European Research Council [293544]
  2. Wellcome Trust [WT100269AIA]
  3. Medical Research Council [G0800575]
  4. Royal Society-USA/Canada Exchange Fellowship
  5. UK Multiple Sclerosis Society
  6. Wellcome Trust
  7. European Research Council (ERC) [293544] Funding Source: European Research Council (ERC)
  8. Medical Research Council [G0800575, MC_PC_12009] Funding Source: researchfish
  9. Rosetrees Trust [M144] Funding Source: researchfish
  10. Wellcome Trust [100269/Z/12/Z] Funding Source: researchfish
  11. MRC [G0800575] Funding Source: UKRI

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Remyelination is the regenerative response to demyelination. Although the oligodendrocyte progenitor is established as the major source of remyelinating cells, there is no conclusive evidence on whether mature, differentiated oligodendrocytes can also contribute to remyelination. Using two different inducible myelin-CreER mouse strains in which mature oligodendrocytes were prelabeled by the expression of membrane-bound Green fluorescent protein, we found that after focal spinal cord demyelination, the surrounding surviving labeled oligodendrocytes did not proliferate but remained at a consistent density. Furthermore, existing (prelabeled) oligodendrocytes showed no evidence of incorporation or migration into the lesioned area, or of process extension from the peripheral margins into the lesion. Thus, mature oligodendrocytes do not normally contribute to remyelination and are therefore not a promising target for regenerative therapy.

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