4.6 Article

Large-scale electron microscopic volume imaging of interfascicular oligodendrocytes in the mouse corpus callosum

Journal

GLIA
Volume 69, Issue 10, Pages 2488-2502

Publisher

WILEY
DOI: 10.1002/glia.24055

Keywords

axon; corpus callosum; myelin; oligodendrocyte; SBF-SEM

Categories

Funding

  1. Cooperative Study Programs of the National Institute for Physiological Sciences
  2. KAKENHI [JP17H05774]
  3. Osaka Foundation for Promotion of Fundamental Medical Research
  4. National Center of Neurology and Psychiatry [3-5, 30-5]
  5. [JP16H06280]

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Single oligodendrocytes in the central nervous system produce myelin sheaths around multiple axons, and interfascicular oligodendrocytes (IOs) in the corpus callosum of adult mice have morphologically polarized cell bodies with processes of different thicknesses for myelinating axons. The myelin sheaths originating from specific IOs have biased thicknesses and are associated with axonal diameter. Despite potential axonal regulation of myelin sheath thickness, a single axon may also independently influence myelin thickness.
Single oligodendrocytes produce myelin sheaths around multiple axons in the central nervous system. Interfascicular oligodendrocytes (IOs) facilitate nerve conduction, but their detailed morphologies remain largely unknown. In the present study, we three-dimensionally reconstructed IOs in the corpus callosum of adult mouse using serial block face scanning electron microscopy. The cell bodies of IOs were morphologically polarized and extended thick processes from the cytoplasm-rich part of the cell. Processes originating from the cell body of each IO can be classified into two types: one myelinates an axon without branching, while the other type branches and each branch myelinates a distinct axon. Myelin sheaths originating from a particular IO have biased thicknesses, wrapping axons of a limited range of diameters. Consistent with this finding, IOs transduced and visualized with a rabies viral vector expressing GFP showed statistically significant variation in their myelination patterns. We further reconstructed the sheath immediately adjacent to that derived from each of the analyzed IOs; the thicknesses of the pair of sheaths were significantly correlated despite emanating from different IOs. These results suggest that a single axon could regulate myelin sheath thicknesses, even if the sheaths are derived from distinct IOs. Collectively, our results indicate that the IOs have their own myelin profiles defined by myelin thickness and axonal diameter although axons may regulate thickness of myelin sheath.

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