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The expression of Netrin-1 in the MIA-induced osteoarthritic temporomandibular joint in mice

Subchondral bone degeneration is the main pathological change during temporomandibular joint (TMJ) osteoarthritis (OA) development. Netrin-1, an axon-guiding factor, might play roles in OA development and pain. The purpose of this study was to investigate the expression of Netrin-1 in TMJ OA and its...

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Autores principales: Xiao, Mian, Hu, Zhihui, Jiang, Henghua, Li, Cheng, Guo, Huilin, Fang, Wei, Long, Xing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8333414/
https://www.ncbi.nlm.nih.gov/pubmed/34344989
http://dx.doi.org/10.1038/s41598-021-95251-9
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author Xiao, Mian
Hu, Zhihui
Jiang, Henghua
Li, Cheng
Guo, Huilin
Fang, Wei
Long, Xing
author_facet Xiao, Mian
Hu, Zhihui
Jiang, Henghua
Li, Cheng
Guo, Huilin
Fang, Wei
Long, Xing
author_sort Xiao, Mian
collection PubMed
description Subchondral bone degeneration is the main pathological change during temporomandibular joint (TMJ) osteoarthritis (OA) development. Netrin-1, an axon-guiding factor, might play roles in OA development and pain. The purpose of this study was to investigate the expression of Netrin-1 in TMJ OA and its possible role in the progression of TMJ OA and pain. The synovial fluids of temporomandibular joint disorders (TMDs) patients were collected for Netrin-1 by enzyme linked immunosorbent assay (ELISA). TMJ OA model was built by MIA joint injection, and then the von Frey test, hematoxylin & eosin (H&E) staining, toluidine blue (TB) staining, immunohistochemical (IHC) staining and micro-CT were performed. After induction of osteoclast differentiation of raw264.7 cells, immunofluorescence (IF) was used to detect the Netrin-1 and its receptors on osteoclast membrane. The concentration of Netrin-1 increased in the synovial fluid of TMJ OA patients. After MIA injection to TMJ, the head withdrawal threshold (HWT) was significantly decreased. Microscopically, the structural disorder of subchondral bone was the most obvious at the 2nd week after MIA injection. In addition, Netrin-1 expression increased in the subchondral bone at the 2nd week after MIA injection. In vitro, the expressions of Netrin-1 and its receptor Unc5B were upregulated on the osteoclast membrane. Netrin-1 might be an important regulator during bone degeneration and pain in the process of TMJ OA.
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spelling pubmed-83334142021-08-05 The expression of Netrin-1 in the MIA-induced osteoarthritic temporomandibular joint in mice Xiao, Mian Hu, Zhihui Jiang, Henghua Li, Cheng Guo, Huilin Fang, Wei Long, Xing Sci Rep Article Subchondral bone degeneration is the main pathological change during temporomandibular joint (TMJ) osteoarthritis (OA) development. Netrin-1, an axon-guiding factor, might play roles in OA development and pain. The purpose of this study was to investigate the expression of Netrin-1 in TMJ OA and its possible role in the progression of TMJ OA and pain. The synovial fluids of temporomandibular joint disorders (TMDs) patients were collected for Netrin-1 by enzyme linked immunosorbent assay (ELISA). TMJ OA model was built by MIA joint injection, and then the von Frey test, hematoxylin & eosin (H&E) staining, toluidine blue (TB) staining, immunohistochemical (IHC) staining and micro-CT were performed. After induction of osteoclast differentiation of raw264.7 cells, immunofluorescence (IF) was used to detect the Netrin-1 and its receptors on osteoclast membrane. The concentration of Netrin-1 increased in the synovial fluid of TMJ OA patients. After MIA injection to TMJ, the head withdrawal threshold (HWT) was significantly decreased. Microscopically, the structural disorder of subchondral bone was the most obvious at the 2nd week after MIA injection. In addition, Netrin-1 expression increased in the subchondral bone at the 2nd week after MIA injection. In vitro, the expressions of Netrin-1 and its receptor Unc5B were upregulated on the osteoclast membrane. Netrin-1 might be an important regulator during bone degeneration and pain in the process of TMJ OA. Nature Publishing Group UK 2021-08-03 /pmc/articles/PMC8333414/ /pubmed/34344989 http://dx.doi.org/10.1038/s41598-021-95251-9 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
Xiao, Mian
Hu, Zhihui
Jiang, Henghua
Li, Cheng
Guo, Huilin
Fang, Wei
Long, Xing
The expression of Netrin-1 in the MIA-induced osteoarthritic temporomandibular joint in mice
title The expression of Netrin-1 in the MIA-induced osteoarthritic temporomandibular joint in mice
title_full The expression of Netrin-1 in the MIA-induced osteoarthritic temporomandibular joint in mice
title_fullStr The expression of Netrin-1 in the MIA-induced osteoarthritic temporomandibular joint in mice
title_full_unstemmed The expression of Netrin-1 in the MIA-induced osteoarthritic temporomandibular joint in mice
title_short The expression of Netrin-1 in the MIA-induced osteoarthritic temporomandibular joint in mice
title_sort expression of netrin-1 in the mia-induced osteoarthritic temporomandibular joint in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8333414/
https://www.ncbi.nlm.nih.gov/pubmed/34344989
http://dx.doi.org/10.1038/s41598-021-95251-9
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