Myelination generates aberrant ultrastructure that is resolved by microglia

Author:

Djannatian Minou1234ORCID,Radha Swathi12ORCID,Weikert Ulrich5ORCID,Safaiyan Shima12ORCID,Wrede Christoph6ORCID,Deichsel Cassandra12ORCID,Kislinger Georg12ORCID,Rhomberg Agata12ORCID,Ruhwedel Torben5ORCID,Campbell Douglas S.12ORCID,van Ham Tjakko7ORCID,Schmid Bettina2ORCID,Hegermann Jan6ORCID,Möbius Wiebke5ORCID,Schifferer Martina24ORCID,Simons Mikael1248ORCID

Affiliation:

1. Institute of Neuronal Cell Biology, Technical University Munich 1 , Munich, Germany

2. German Center for Neurodegenerative Diseases 2 , Munich, Germany

3. 3Department of Neurology, Klinikum rechts der Isar, TUM School of Medicine, Technical University of Munich, Munich, Germany

4. Munich Cluster of Systems Neurology (SyNergy) 4 , Munich, Germany

5. Max-Planck Institute of Experimental Medicine 5 , Göttingen, Germany

6. Institute of Functional and Applied Anatomy, Research Core Unit Electron Microscopy, Hannover Medical School 6 , Hannover, Germany

7. Department of Clinical Genetics, Erasmus University Medical Center, University Medical Center Rotterdam 7 , Rotterdam, Netherlands

8. Institute for Stroke and Dementia Research, University Hospital of Munich, Ludwig Maximilian University of Munich 8 , Munich, Germany

Abstract

To enable rapid propagation of action potentials, axons are ensheathed by myelin, a multilayered insulating membrane formed by oligodendrocytes. Most of the myelin is generated early in development, resulting in the generation of long-lasting stable membrane structures. Here, we explored structural and dynamic changes in central nervous system myelin during development. To achieve this, we performed an ultrastructural analysis of mouse optic nerves by serial block face scanning electron microscopy (SBF-SEM) and confocal time-lapse imaging in the zebrafish spinal cord. We found that myelin undergoes extensive ultrastructural changes during early postnatal development. Myelin degeneration profiles were engulfed and phagocytosed by microglia using exposed phosphatidylserine as one “eat me” signal. In contrast, retractions of entire myelin sheaths occurred independently of microglia and involved uptake of myelin by the oligodendrocyte itself. Our findings show that the generation of myelin early in development is an inaccurate process associated with aberrant ultrastructural features that require substantial refinement.

Funder

German Research Foundation

Human Frontier Science Program

Dr. Miriam and Sheldon G. Adelson Medical Research Foundation

European Research Council

Publisher

Rockefeller University Press

Subject

Cell Biology

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