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Inflammation produced by senescent osteocytes mediates age-related bone loss

PURPOSE: The molecular mechanisms of age-related bone loss are unclear and without valid drugs yet. The aims of this study were to explore the molecular changes that occur in bone tissue during age-related bone loss, to further clarify the changes in function, and to predict potential therapeutic dr...

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Autores principales: Wang, Zixuan, Zhang, Xiaofei, Cheng, Xing, Ren, Tianxing, Xu, Weihua, Li, Jin, Wang, Hui, Zhang, Jinxiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9940315/
https://www.ncbi.nlm.nih.gov/pubmed/36814916
http://dx.doi.org/10.3389/fimmu.2023.1114006
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author Wang, Zixuan
Zhang, Xiaofei
Cheng, Xing
Ren, Tianxing
Xu, Weihua
Li, Jin
Wang, Hui
Zhang, Jinxiang
author_facet Wang, Zixuan
Zhang, Xiaofei
Cheng, Xing
Ren, Tianxing
Xu, Weihua
Li, Jin
Wang, Hui
Zhang, Jinxiang
author_sort Wang, Zixuan
collection PubMed
description PURPOSE: The molecular mechanisms of age-related bone loss are unclear and without valid drugs yet. The aims of this study were to explore the molecular changes that occur in bone tissue during age-related bone loss, to further clarify the changes in function, and to predict potential therapeutic drugs. METHODS: We collected bone tissues from children, middle-aged individuals, and elderly people for protein sequencing and compared the three groups of proteins pairwise, and the differentially expressed proteins (DEPs) in each group were analyzed by Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG). K-means cluster analysis was then used to screen out proteins that continuously increased/decreased with age. Canonical signaling pathways that were activated or inhibited in bone tissue along with increasing age were identified by Ingenuity Pathway Analysis (IPA). Prediction of potential drugs was performed using the Connectivity Map (CMap). Finally, DEPs from sequencing were verified by Western blot, and the drug treatment effect was verified by quantitative real-time PCR. RESULTS: The GO and KEGG analyses show that the DEPs were associated with inflammation and bone formation with aging, and the IPA analysis shows that pathways such as IL-8 signaling and acute-phase response signaling were activated, while glycolysis I and EIF2 signaling were inhibited. A total of nine potential drugs were predicted, with rapamycin ranking the highest. In cellular experiments, rapamycin reduced the senescence phenotype produced by the H(2)O(2)-stimulated osteocyte-like cell MLO-Y4. CONCLUSION: With age, inflammatory pathways are activated in bone tissue, and signals that promote bone formation are inhibited. This study contributes to the understanding of the molecular changes that occur in bone tissue during age-related bone loss and provides evidence that rapamycin is a drug of potential clinical value for this disease. The therapeutic effects of the drug are to be further studied in animals.
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spelling pubmed-99403152023-02-21 Inflammation produced by senescent osteocytes mediates age-related bone loss Wang, Zixuan Zhang, Xiaofei Cheng, Xing Ren, Tianxing Xu, Weihua Li, Jin Wang, Hui Zhang, Jinxiang Front Immunol Immunology PURPOSE: The molecular mechanisms of age-related bone loss are unclear and without valid drugs yet. The aims of this study were to explore the molecular changes that occur in bone tissue during age-related bone loss, to further clarify the changes in function, and to predict potential therapeutic drugs. METHODS: We collected bone tissues from children, middle-aged individuals, and elderly people for protein sequencing and compared the three groups of proteins pairwise, and the differentially expressed proteins (DEPs) in each group were analyzed by Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG). K-means cluster analysis was then used to screen out proteins that continuously increased/decreased with age. Canonical signaling pathways that were activated or inhibited in bone tissue along with increasing age were identified by Ingenuity Pathway Analysis (IPA). Prediction of potential drugs was performed using the Connectivity Map (CMap). Finally, DEPs from sequencing were verified by Western blot, and the drug treatment effect was verified by quantitative real-time PCR. RESULTS: The GO and KEGG analyses show that the DEPs were associated with inflammation and bone formation with aging, and the IPA analysis shows that pathways such as IL-8 signaling and acute-phase response signaling were activated, while glycolysis I and EIF2 signaling were inhibited. A total of nine potential drugs were predicted, with rapamycin ranking the highest. In cellular experiments, rapamycin reduced the senescence phenotype produced by the H(2)O(2)-stimulated osteocyte-like cell MLO-Y4. CONCLUSION: With age, inflammatory pathways are activated in bone tissue, and signals that promote bone formation are inhibited. This study contributes to the understanding of the molecular changes that occur in bone tissue during age-related bone loss and provides evidence that rapamycin is a drug of potential clinical value for this disease. The therapeutic effects of the drug are to be further studied in animals. Frontiers Media S.A. 2023-02-06 /pmc/articles/PMC9940315/ /pubmed/36814916 http://dx.doi.org/10.3389/fimmu.2023.1114006 Text en Copyright © 2023 Wang, Zhang, Cheng, Ren, Xu, Li, Wang and Zhang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Wang, Zixuan
Zhang, Xiaofei
Cheng, Xing
Ren, Tianxing
Xu, Weihua
Li, Jin
Wang, Hui
Zhang, Jinxiang
Inflammation produced by senescent osteocytes mediates age-related bone loss
title Inflammation produced by senescent osteocytes mediates age-related bone loss
title_full Inflammation produced by senescent osteocytes mediates age-related bone loss
title_fullStr Inflammation produced by senescent osteocytes mediates age-related bone loss
title_full_unstemmed Inflammation produced by senescent osteocytes mediates age-related bone loss
title_short Inflammation produced by senescent osteocytes mediates age-related bone loss
title_sort inflammation produced by senescent osteocytes mediates age-related bone loss
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9940315/
https://www.ncbi.nlm.nih.gov/pubmed/36814916
http://dx.doi.org/10.3389/fimmu.2023.1114006
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