Reflective imaging of myelin integrity in the human and mouse central nervous systems

Front Cell Neurosci. 2024 Jul 10:18:1408182. doi: 10.3389/fncel.2024.1408182. eCollection 2024.

Abstract

The structural integrity of myelin sheaths in the central nervous system (CNS) is crucial for the maintenance of its function. Electron microscopy (EM) is the gold standard for visualizing individual myelin sheaths. However, the tissue processing involved can induce artifacts such as shearing of myelin, which can be difficult to distinguish from true myelin abnormalities. Spectral confocal reflectance (SCoRe) microscopy is an imaging technique that leverages the differential refractive indices of compacted CNS myelin in comparison to surrounding parenchyma to detect individual compact myelin internodes with reflected light, positioning SCoRe as a possible complementary method to EM to assess myelin integrity. Whether SCoRe is sensitive enough to detect losses in myelin compaction when myelin quantity is otherwise unaffected has not yet been directly tested. Here, we assess the capacity of SCoRe to detect differences in myelin compaction in two mouse models that exhibit a loss of myelin compaction without demyelination: microglia-deficient mice (Csf1r-FIRE Δ) and wild-type mice fed with the CSF1R inhibitor PLX5622. In addition, we compare the ability to detect compact myelin sheaths using SCoRe in fixed-frozen versus paraffin-embedded mouse tissue. Finally, we show that SCoRe can successfully detect individual sheaths in aged human paraffin-embedded samples of deep white matter regions. As such, we find SCoRe to be an attractive technique to investigate myelin integrity, with sufficient sensitivity to detect myelin ultrastructural abnormalities and the ability to perform equally well in tissue preserved using different methods.

Keywords: compaction; imaging; myelin; oligodendrocyte; reflectance.

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This study was funded by the John David Eaton Chair in Multiple Sclerosis Research and the Hall-Sloan Multiple Sclerosis Basic Research Fund (to VM), and a Medical Research Council Senior Non-Clinical Fellowship (to VM). The Lothian Birth Cohort 1936 was supported by the BBSRC and ESRC [BB/W008793/1], Age UK (Disconnected Mind Project), the Milton Damerel Trust, the MRC (MR/M01311/1; MR/R024065/1), and the University of Edinburgh. SC was supported by a Sir Henry Dale Fellowship jointly funded by the Wellcome Trust and the Royal Society [221890/Z/20/Z]. AH holds a Walter Benjamin postdoctoral fellowship from the German Research Foundation (Deutsche Forschungsgemeinschaft (DFG) – 498972649).