4.8 Article

Myelination induces axonal hotspots of synaptic vesicle fusion that promote sheath growth

期刊

CURRENT BIOLOGY
卷 31, 期 17, 页码 3743-+

出版社

CELL PRESS
DOI: 10.1016/j.cub.2021.06.036

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资金

  1. Medical Research Council (MRC) [MR/P006272/1]
  2. Wellcome Trust [102836/Z/13/Z, 214244/Z/18/Z, 108906/Z/15/Z, 101195/Z/13/Z]
  3. University of Edinburgh PhD Tissue Repair Studentship Award [MR/K501293/1]
  4. Royal Society
  5. UCL Excellence Fellowship
  6. MRC [MR/P006272/1] Funding Source: UKRI
  7. Wellcome Trust [101195/Z/13/Z, 214244/Z/18/Z] Funding Source: Wellcome Trust

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The research indicates that synaptic vesicle fusion plays a crucial role in the process of myelination, promoting the activity-regulated signal in neurons and consolidating sheath growth on specific axons. Axonal vesicular fusion increases significantly during myelination, impacting the formation and growth of myelin sheaths.
Myelination of axons by oligodendrocytes enables fast saltatory conduction. Oligodendrocytes are responsive to neuronal activity, which has been shown to induce changes to myelin sheaths, potentially to optimize conduction and neural circuit function. However, the cellular bases of activity-regulated myelination in vivo are unclear, partly due to the difficulty of analyzing individual myelinated axons over time. Activity-regulated myelination occurs in specific neuronal subtypes and can be mediated by synaptic vesicle fusion, but several questions remain: it is unclear whether vesicular fusion occurs stochastically along axons or in discrete hotspots during myelination and whether vesicular fusion regulates myelin targeting, formation, and/or growth. It is also unclear why some neurons, but not others, exhibit activity regulated myelination. Here, we imaged synaptic vesicle fusion in individual neurons in living zebrafish and documented robust vesicular fusion along axons during myelination. Surprisingly, we found that axonal vesicular fusion increased upon and required myelination. We found that axonal vesicular fusion was enriched in hotspots, namely the heminodal non-myelinated domains into which sheaths grew. Blocking vesicular fusion reduced the stable formation and growth of myelin sheaths, and chemogenetically stimulating neuronal activity promoted sheath growth. Finally, we observed high levels of axonal vesicular fusion only in neuronal subtypes that exhibit activity-regulated myelination. Our results identify a novel feedforwardmechanism whereby the process of myelination promotes the neuronal activity regulated signal, vesicular fusion that, in turn, consolidates sheath growth along specific axons selected for myelination.

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