@article{74139cc90a904d0480eded8a180fac85,
title = "Nile Red fluorescence spectroscopy reports early physicochemical changes in myelin with high sensitivity",
abstract = "The molecular composition of myelin membranes determines their structure and function. Even minute changes to the biochemical balance can have profound consequences for axonal conduction and the synchronicity of neural networks. Hypothesizing that the earliest indication of myelin injury involves changes in the composition and/or polarity of its constituent lipids, we developed a sensitive spectroscopic technique for defining the chemical polarity of myelin lipids in fixed frozen tissue sections from rodent and human. The method uses a simple staining procedure involving the lipophilic dye Nile Red, whose fluorescence spectrum varies according to the chemical polarity of the microenvironment into which the dye embeds. Nile Red spectroscopy identified histologically intact yet biochemically altered myelin in prelesioned tissues, including mouse white matter following subdemyelinating cuprizone intoxication, as well as normal-appearing white matter in multiple sclerosis brain. Nile Red spectroscopy offers a relatively simple yet highly sensitive technique for detecting subtle myelin changes.",
keywords = "Cuprizone, Fluorescence spectroscopy, Lipids, Multiple sclerosis, Spectral confocal microscopy",
author = "Wulin Teo and Caprariello, {Andrew V.} and Morgan, {Megan L.} and Antonio Luchicchi and Schenk, {Geert J.} and Joseph, {Jeffrey T.} and Geurts, {Jeroen J.G.} and Stys, {Peter K.}",
note = "Funding Information: ACKNOWLEDGMENTS. This work was supported by grants from Canadian Institutes for Health Research, the MS Society of Canada, Canada Research Chairs, and Canada Foundation for Innovation to P.K.S.; Stichting MS Research/ Stichting Klimmen tegen MS (MoveS) (pilot project number 16‐954a/b MS), and Ammodo KNAW award (2017) to J.J.G.G.; and Stichting MS Research (Monique Blom‐de Wagt grant, 18‐997 MS) to A.L. We acknowledge the Hotchkiss Brain Institute Advanced Microscopy Platform and the Cumming School of Medicine for support and use of the Nikon A1RMP spectral confocal microscope; and the slide scanning equipment at the Live Cell Imaging Resource Laboratory, Snyder Institute for Chronic Disease, Cumming School of Medicine. We thank Dr. C. Brideau for assistance with construction of the GUV-generating apparatus and Dr. Y. Hernandez for assistance with culturing MO3.13 cells. Publisher Copyright: {\textcopyright} 2021 National Academy of Sciences. All rights reserved. Copyright: Copyright 2021 Elsevier B.V., All rights reserved.",
year = "2021",
month = feb,
day = "23",
doi = "https://doi.org/10.1073/pnas.2016897118",
language = "English",
volume = "118",
journal = "PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA",
issn = "0027-8424",
publisher = "National Acad Sciences",
number = "8",
}