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Circulating Exosomes from Mice with LPS-Induced Bone Loss Inhibit Osteoblast Differentiation
Osteoimmunology focuses on the intermodulation between bone and the immune system. Lipopolysaccharide (LPS)-induced bone loss models are commonly used to investigate the interface between inflammation and osteoporosis. Circulating exosomes can regulate physiological and pathological processes throug...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9300544/ https://www.ncbi.nlm.nih.gov/pubmed/35435443 http://dx.doi.org/10.1007/s00223-022-00977-x |
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author | Wang, Yixuan Zhang, Lijun Wang, Ke Zhou, Hua Li, Gaozhi Xu, Liqun Hu, Zebing Cao, Xinsheng Shi, Fei Zhang, Shu |
author_facet | Wang, Yixuan Zhang, Lijun Wang, Ke Zhou, Hua Li, Gaozhi Xu, Liqun Hu, Zebing Cao, Xinsheng Shi, Fei Zhang, Shu |
author_sort | Wang, Yixuan |
collection | PubMed |
description | Osteoimmunology focuses on the intermodulation between bone and the immune system. Lipopolysaccharide (LPS)-induced bone loss models are commonly used to investigate the interface between inflammation and osteoporosis. Circulating exosomes can regulate physiological and pathological processes through exosomal microRNAs and proteins. In this study, we observed reduced osteoblast number and bone formation in LPS-induced bone loss mice (LPS mice). Levels of circulating exosomes were increased by ~ twofold in LPS mice, and the expression of exosomal miRNAs was significantly changed. miRNAs (miRNA-125b-5p, miRNA-132-3p, and miRNA-214-3p) that were reported to inhibit osteoblast activity were significantly increased in the serum exosomes and bone tissues of LPS mice. Additionally, LPS-induced increases in exosomes significantly inhibited the osteogenic differentiation of MC3T3-E1 cells. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00223-022-00977-x. |
format | Online Article Text |
id | pubmed-9300544 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-93005442022-07-22 Circulating Exosomes from Mice with LPS-Induced Bone Loss Inhibit Osteoblast Differentiation Wang, Yixuan Zhang, Lijun Wang, Ke Zhou, Hua Li, Gaozhi Xu, Liqun Hu, Zebing Cao, Xinsheng Shi, Fei Zhang, Shu Calcif Tissue Int Original Research Osteoimmunology focuses on the intermodulation between bone and the immune system. Lipopolysaccharide (LPS)-induced bone loss models are commonly used to investigate the interface between inflammation and osteoporosis. Circulating exosomes can regulate physiological and pathological processes through exosomal microRNAs and proteins. In this study, we observed reduced osteoblast number and bone formation in LPS-induced bone loss mice (LPS mice). Levels of circulating exosomes were increased by ~ twofold in LPS mice, and the expression of exosomal miRNAs was significantly changed. miRNAs (miRNA-125b-5p, miRNA-132-3p, and miRNA-214-3p) that were reported to inhibit osteoblast activity were significantly increased in the serum exosomes and bone tissues of LPS mice. Additionally, LPS-induced increases in exosomes significantly inhibited the osteogenic differentiation of MC3T3-E1 cells. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00223-022-00977-x. Springer US 2022-04-18 2022 /pmc/articles/PMC9300544/ /pubmed/35435443 http://dx.doi.org/10.1007/s00223-022-00977-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 | Original Research Wang, Yixuan Zhang, Lijun Wang, Ke Zhou, Hua Li, Gaozhi Xu, Liqun Hu, Zebing Cao, Xinsheng Shi, Fei Zhang, Shu Circulating Exosomes from Mice with LPS-Induced Bone Loss Inhibit Osteoblast Differentiation |
title | Circulating Exosomes from Mice with LPS-Induced Bone Loss Inhibit Osteoblast Differentiation |
title_full | Circulating Exosomes from Mice with LPS-Induced Bone Loss Inhibit Osteoblast Differentiation |
title_fullStr | Circulating Exosomes from Mice with LPS-Induced Bone Loss Inhibit Osteoblast Differentiation |
title_full_unstemmed | Circulating Exosomes from Mice with LPS-Induced Bone Loss Inhibit Osteoblast Differentiation |
title_short | Circulating Exosomes from Mice with LPS-Induced Bone Loss Inhibit Osteoblast Differentiation |
title_sort | circulating exosomes from mice with lps-induced bone loss inhibit osteoblast differentiation |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9300544/ https://www.ncbi.nlm.nih.gov/pubmed/35435443 http://dx.doi.org/10.1007/s00223-022-00977-x |
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