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Macroscopic detection of demyelinated lesions in mouse PNS with neutral red dye
Lysophosphatidylcholine (LPC)-induced demyelination is a versatile animal model that is frequently used to identify and examine molecular pathways of demyelination and remyelination in the central (CNS) and peripheral nervous system (PNS). However, identification of focally demyelinated lesion had b...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8377033/ https://www.ncbi.nlm.nih.gov/pubmed/34413421 http://dx.doi.org/10.1038/s41598-021-96395-4 |
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author | Yamazaki, Reiji Osanai, Yasuyuki Kouki, Tom Shinohara, Yoshiaki Huang, Jeffrey K. Ohno, Nobuhiko |
author_facet | Yamazaki, Reiji Osanai, Yasuyuki Kouki, Tom Shinohara, Yoshiaki Huang, Jeffrey K. Ohno, Nobuhiko |
author_sort | Yamazaki, Reiji |
collection | PubMed |
description | Lysophosphatidylcholine (LPC)-induced demyelination is a versatile animal model that is frequently used to identify and examine molecular pathways of demyelination and remyelination in the central (CNS) and peripheral nervous system (PNS). However, identification of focally demyelinated lesion had been difficult and usually required tissue fixation, sectioning and histological analysis. Recently, a method for labeling and identification of demyelinated lesions in the CNS by intraperitoneal injection of neutral red (NR) dye was developed. However, it remained unknown whether NR can be used to label demyelinated lesions in PNS. In this study, we generated LPC-induced demyelination in sciatic nerve of mice, and demonstrated that the demyelinated lesions at the site of LPC injection were readily detectable at 7 days postlesion (dpl) by macroscopic observation of NR labeling. Moreover, NR staining gradually decreased from 7 to 21 dpl over the course of remyelination. Electron microscopy analysis of NR-labeled sciatic nerves at 7 dpl confirmed demyelination and myelin debris in lesions. Furthermore, fluorescence microscopy showed NR co-labeling with activated macrophages and Schwann cells in the PNS lesions. Together, NR labeling is a straightforward method that allows the macroscopic detection of demyelinated lesions in sciatic nerves after LPC injection. |
format | Online Article Text |
id | pubmed-8377033 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-83770332021-08-27 Macroscopic detection of demyelinated lesions in mouse PNS with neutral red dye Yamazaki, Reiji Osanai, Yasuyuki Kouki, Tom Shinohara, Yoshiaki Huang, Jeffrey K. Ohno, Nobuhiko Sci Rep Article Lysophosphatidylcholine (LPC)-induced demyelination is a versatile animal model that is frequently used to identify and examine molecular pathways of demyelination and remyelination in the central (CNS) and peripheral nervous system (PNS). However, identification of focally demyelinated lesion had been difficult and usually required tissue fixation, sectioning and histological analysis. Recently, a method for labeling and identification of demyelinated lesions in the CNS by intraperitoneal injection of neutral red (NR) dye was developed. However, it remained unknown whether NR can be used to label demyelinated lesions in PNS. In this study, we generated LPC-induced demyelination in sciatic nerve of mice, and demonstrated that the demyelinated lesions at the site of LPC injection were readily detectable at 7 days postlesion (dpl) by macroscopic observation of NR labeling. Moreover, NR staining gradually decreased from 7 to 21 dpl over the course of remyelination. Electron microscopy analysis of NR-labeled sciatic nerves at 7 dpl confirmed demyelination and myelin debris in lesions. Furthermore, fluorescence microscopy showed NR co-labeling with activated macrophages and Schwann cells in the PNS lesions. Together, NR labeling is a straightforward method that allows the macroscopic detection of demyelinated lesions in sciatic nerves after LPC injection. Nature Publishing Group UK 2021-08-19 /pmc/articles/PMC8377033/ /pubmed/34413421 http://dx.doi.org/10.1038/s41598-021-96395-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Yamazaki, Reiji Osanai, Yasuyuki Kouki, Tom Shinohara, Yoshiaki Huang, Jeffrey K. Ohno, Nobuhiko Macroscopic detection of demyelinated lesions in mouse PNS with neutral red dye |
title | Macroscopic detection of demyelinated lesions in mouse PNS with neutral red dye |
title_full | Macroscopic detection of demyelinated lesions in mouse PNS with neutral red dye |
title_fullStr | Macroscopic detection of demyelinated lesions in mouse PNS with neutral red dye |
title_full_unstemmed | Macroscopic detection of demyelinated lesions in mouse PNS with neutral red dye |
title_short | Macroscopic detection of demyelinated lesions in mouse PNS with neutral red dye |
title_sort | macroscopic detection of demyelinated lesions in mouse pns with neutral red dye |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8377033/ https://www.ncbi.nlm.nih.gov/pubmed/34413421 http://dx.doi.org/10.1038/s41598-021-96395-4 |
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