Abstract

IntroductionIn the human demyelinating central nervous system (CNS) disease multiple sclerosis, remyelination promotes recovery and limits neurodegeneration, but this is inefficient and always ultimately fails. Furthermore, these regenerated myelin sheaths are thinner and shorter than the original, leaving the underlying axons potentially vulnerable. In rodent models, CNS remyelination is more efficient, so that in young animals (but not old) the number of myelinated axons is efficiently restored to normal, but in both young and old rodents, regenerated myelin sheaths are still short and thin. The reasons for these differences in remyelination efficiency, the thinner remyelinated myelin sheaths compared to developmental myelin and the subsequent effect on the underlying axon are unclear. We studied CNS remyelination in the highly regenerative adult zebrafish (Danio rerio), to better understand mechanisms of what we hypothesised would be highly efficient remyelination, and to identify differences to mammalian CNS remyelination, as larval zebrafish are increasingly used for high throughput screens to identify potential drug targets to improve myelination and remyelination.ResultsWe developed a novel method to induce a focal demyelinating lesion in adult zebrafish optic nerve with no discernible axonal damage, and describe the cellular changes over time. Remyelination is indeed efficient in both young and old adult zebrafish optic nerves, and at 4 weeks after demyelination, the number of myelinated axons is restored to normal, but internode lengths are short. However, unlike in rodents or in humans, in young zebrafish these regenerated myelin sheaths were of normal thickness, whereas in aged zebrafish, they were thin, and remained so even 3 months later. This inability to restore normal myelin thickness in remyelination with age was associated with a reduced macrophage/microglial response.ConclusionZebrafish are able to efficiently restore normal thickness myelin around optic nerve axons after demyelination, unlike in mammals. However, this fails with age, when only thin myelin is achieved. This gives us a novel model to try and dissect the mechanism for restoring myelin thickness in CNS remyelination.

Highlights

  • In the human demyelinating central nervous system (CNS) disease multiple sclerosis, remyelination promotes recovery and limits neurodegeneration, but this is inefficient and always fails

  • Lysophosphatidylcholine (LPC) treatment of the adult zebrafish optic nerve leads to a focal demyelinating lesion followed by remyelination within 4 weeks crush lesions of the optic nerve of zebrafish to study re-establishment of myelin on regenerated axons have been carried out previously [39,40], these studies do not assess remyelination, because myelination of a newly generated axonal sprout may show differences to remyelination of a demyelinated axon

  • We used the myelinotoxin LPC, as it has been used extensively in rodent models of demyelination. This was soaked onto a small piece of absorbent gelatin foam placed next to the adult zebrafish optic nerve to produce focal demyelination; the contralateral optic nerve served as an internal control

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Summary

Introduction

In the human demyelinating central nervous system (CNS) disease multiple sclerosis, remyelination promotes recovery and limits neurodegeneration, but this is inefficient and always fails. Remyelination in the rodent CNS after toxin mediated demyelinating injury is efficient, so that in young rodents the proportion of axons with a myelin sheath in lesions is restored to that seen in control animals, though this ability reduces with age, associated with impaired oligodendrocyte progenitor cell recruitment and differentiation into myelin forming oligodendrocytes in older animals [14,15]. In both young and old rodents, as in humans, regenerated myelin sheaths are thin and short [16,17]

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