AI Article Synopsis

  • Myelination increases the speed and efficiency of action potentials around neuronal axons, but neuronal somata and dendrites do not get myelinated despite the ability of oligodendrocytes to do so.
  • Disrupting neuron-oligodendrocyte communication leads to unexpected myelination in the somatodendritic area, indicating the presence of inhibitory signals needed to prevent this.
  • The study identifies neuronal junction adhesion molecule 2 (JAM2) as a key molecule that inhibits non-axonal myelination, suggesting a model where myelination is carefully regulated by local signals.

Article Abstract

Myelination occurs selectively around neuronal axons to increase the efficiency and velocity of action potentials. While oligodendrocytes are capable of myelinating permissive structures in the absence of molecular cues, structurally permissive neuronal somata and dendrites remain unmyelinated. Utilizing a purified spinal cord neuron-oligodendrocyte myelinating co-culture system, we demonstrate that disruption of dynamic neuron-oligodendrocyte signaling by chemical cross-linking results in aberrant myelination of the somatodendritic compartment of neurons. We hypothesize that an inhibitory somatodendritic cue is necessary to prevent non-axonal myelination. Using next-generation sequencing and candidate profiling, we identify neuronal junction adhesion molecule 2 (JAM2) as an inhibitory myelin-guidance molecule. Taken together, our results demonstrate that the somatodendritic compartment directly inhibits myelination and suggest a model in which broadly indiscriminate myelination is tailored by inhibitory signaling to meet local myelination requirements.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4990461PMC
http://dx.doi.org/10.1016/j.neuron.2016.07.021DOI Listing

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