Li Tang, Yangying Duan, Ke Yang, Dong Wang, Huan Yao
{"title":"LIPUS通过FOXO1保护PDLSCs免受氧化损伤并促进牙槽骨再生。","authors":"Li Tang, Yangying Duan, Ke Yang, Dong Wang, Huan Yao","doi":"10.1111/odi.70019","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>Oxidative stress is regarded as a significant element contributing to periodontal tissue destruction and impaired regeneration. Low-intensity pulsed ultrasound (LIPUS) has been shown to effectively protect periodontal ligament stem cells (PDLSCs) from oxidative damage. However, the potential molecular mechanism of LIPUS remains unclear.</p><p><strong>Methods: </strong>The experimental periodontitis model was established by ligation. The expression levels of oxidative stress and osteogenic markers in vivo were detected by immunohistochemistry. PDLSCs were incubated with H<sub>2</sub>O<sub>2</sub> to imitate oxidative stress. A reactive oxygen species assay kit was used to determine oxidative stress status. The expression of osteogenic differentiation protein, Forkhead transcription factor-1 (FOXO1) and antioxidant protein was observed by Western blotting. SiRNA technology and the small molecule inhibitor AS1842856 were used to evaluate the role of FOXO1 in LIPUS treatment.</p><p><strong>Results: </strong>The results demonstrated that LIPUS exerts a protective effect against oxidative damage in PDLSCs, reduces alveolar bone loss, and significantly inhibits the elevated phosphorylation levels of FOXO1 in the oxidative stress microenvironment. Moreover, the increased phosphorylation level of FOXO1 diminishes the protective effect of LIPUS.</p><p><strong>Conclusion: </strong>Thus, these results suggest that FOXO1 may be a critical target for LIPUS to attenuate oxidative stress and regulate alveolar bone homeostasis in periodontitis.</p>","PeriodicalId":19615,"journal":{"name":"Oral diseases","volume":" ","pages":""},"PeriodicalIF":2.9000,"publicationDate":"2025-07-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"LIPUS Protects PDLSCs From Oxidative Damage and Promotes Alveolar Bone Regeneration via FOXO1.\",\"authors\":\"Li Tang, Yangying Duan, Ke Yang, Dong Wang, Huan Yao\",\"doi\":\"10.1111/odi.70019\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>Oxidative stress is regarded as a significant element contributing to periodontal tissue destruction and impaired regeneration. Low-intensity pulsed ultrasound (LIPUS) has been shown to effectively protect periodontal ligament stem cells (PDLSCs) from oxidative damage. However, the potential molecular mechanism of LIPUS remains unclear.</p><p><strong>Methods: </strong>The experimental periodontitis model was established by ligation. The expression levels of oxidative stress and osteogenic markers in vivo were detected by immunohistochemistry. PDLSCs were incubated with H<sub>2</sub>O<sub>2</sub> to imitate oxidative stress. A reactive oxygen species assay kit was used to determine oxidative stress status. The expression of osteogenic differentiation protein, Forkhead transcription factor-1 (FOXO1) and antioxidant protein was observed by Western blotting. SiRNA technology and the small molecule inhibitor AS1842856 were used to evaluate the role of FOXO1 in LIPUS treatment.</p><p><strong>Results: </strong>The results demonstrated that LIPUS exerts a protective effect against oxidative damage in PDLSCs, reduces alveolar bone loss, and significantly inhibits the elevated phosphorylation levels of FOXO1 in the oxidative stress microenvironment. Moreover, the increased phosphorylation level of FOXO1 diminishes the protective effect of LIPUS.</p><p><strong>Conclusion: </strong>Thus, these results suggest that FOXO1 may be a critical target for LIPUS to attenuate oxidative stress and regulate alveolar bone homeostasis in periodontitis.</p>\",\"PeriodicalId\":19615,\"journal\":{\"name\":\"Oral diseases\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":2.9000,\"publicationDate\":\"2025-07-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Oral diseases\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1111/odi.70019\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"DENTISTRY, ORAL SURGERY & MEDICINE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Oral diseases","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1111/odi.70019","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"DENTISTRY, ORAL SURGERY & MEDICINE","Score":null,"Total":0}
LIPUS Protects PDLSCs From Oxidative Damage and Promotes Alveolar Bone Regeneration via FOXO1.
Objective: Oxidative stress is regarded as a significant element contributing to periodontal tissue destruction and impaired regeneration. Low-intensity pulsed ultrasound (LIPUS) has been shown to effectively protect periodontal ligament stem cells (PDLSCs) from oxidative damage. However, the potential molecular mechanism of LIPUS remains unclear.
Methods: The experimental periodontitis model was established by ligation. The expression levels of oxidative stress and osteogenic markers in vivo were detected by immunohistochemistry. PDLSCs were incubated with H2O2 to imitate oxidative stress. A reactive oxygen species assay kit was used to determine oxidative stress status. The expression of osteogenic differentiation protein, Forkhead transcription factor-1 (FOXO1) and antioxidant protein was observed by Western blotting. SiRNA technology and the small molecule inhibitor AS1842856 were used to evaluate the role of FOXO1 in LIPUS treatment.
Results: The results demonstrated that LIPUS exerts a protective effect against oxidative damage in PDLSCs, reduces alveolar bone loss, and significantly inhibits the elevated phosphorylation levels of FOXO1 in the oxidative stress microenvironment. Moreover, the increased phosphorylation level of FOXO1 diminishes the protective effect of LIPUS.
Conclusion: Thus, these results suggest that FOXO1 may be a critical target for LIPUS to attenuate oxidative stress and regulate alveolar bone homeostasis in periodontitis.
期刊介绍:
Oral Diseases is a multidisciplinary and international journal with a focus on head and neck disorders, edited by leaders in the field, Professor Giovanni Lodi (Editor-in-Chief, Milan, Italy), Professor Stefano Petti (Deputy Editor, Rome, Italy) and Associate Professor Gulshan Sunavala-Dossabhoy (Deputy Editor, Shreveport, LA, USA). The journal is pre-eminent in oral medicine. Oral Diseases specifically strives to link often-isolated areas of dentistry and medicine through broad-based scholarship that includes well-designed and controlled clinical research, analytical epidemiology, and the translation of basic science in pre-clinical studies. The journal typically publishes articles relevant to many related medical specialties including especially dermatology, gastroenterology, hematology, immunology, infectious diseases, neuropsychiatry, oncology and otolaryngology. The essential requirement is that all submitted research is hypothesis-driven, with significant positive and negative results both welcomed. Equal publication emphasis is placed on etiology, pathogenesis, diagnosis, prevention and treatment.