{"title":"剪切应力预处理提高牙周韧带干细胞存活率","authors":"Ravipha Suwittayarak , Nuttha Klincumhom , Chaloemrit Phrueksotsai , Nuttapol Limjeerajarus , Chalida Nakalekha Limjeerajarus , Hiroshi Egusa , Thanaphum Osathanon","doi":"10.1016/j.archoralbio.2025.106232","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><div>The study investigated <em>in vitro</em> the influences of shear stress preconditioning on human periodontal ligament stem cells (hPDLSCs) under serum deprivation.</div></div><div><h3>Design</h3><div>hPDLSCs were subjected to shear stress at 0.5 and 5 dyn/cm², both with and without serum starvation. Cell viability and apoptosis were assessed using the Resazurin assay and flow cytometry analysis, respectively. Gene and protein expressions were analysed by real-time polymerase chain reaction, immunofluorescent staining, and Western blotting.</div></div><div><h3>Results</h3><div>Our results revealed that shear stress potentially mitigated serum derivation-induced cell death by inducing cell viability, enhancing colony formation, and inhibiting cell apoptosis. The addition of an ERK inhibitor inhibited the shear stress-induced cell apoptosis resistance. Shear stress treatment upregulated cell viability-related gene expression, including <em>SOX2</em>, <em>SOD1</em> and <em>BIRC5.</em> In particular, shear stress promoted the nuclear translocation of SOX2. Meanwhile, the expression of <em>BIRC5</em> was not inhibited by cycloheximide. Shear stress-induced <em>SOX2</em> and <em>BIRC5</em> expression was attenuated by PI3K and ERK inhibitors, respectively.</div></div><div><h3>Conclusions</h3><div>Shear stress contributes to promoting <em>SOX2</em> and <em>BIRC5</em> expression by hPDLSCs, implicating the promotion of stemness and cell survival under serum starvation.</div></div>","PeriodicalId":8288,"journal":{"name":"Archives of oral biology","volume":"173 ","pages":"Article 106232"},"PeriodicalIF":2.2000,"publicationDate":"2025-03-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Shear stress preconditioning enhances periodontal ligament stem cell survival\",\"authors\":\"Ravipha Suwittayarak , Nuttha Klincumhom , Chaloemrit Phrueksotsai , Nuttapol Limjeerajarus , Chalida Nakalekha Limjeerajarus , Hiroshi Egusa , Thanaphum Osathanon\",\"doi\":\"10.1016/j.archoralbio.2025.106232\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Objective</h3><div>The study investigated <em>in vitro</em> the influences of shear stress preconditioning on human periodontal ligament stem cells (hPDLSCs) under serum deprivation.</div></div><div><h3>Design</h3><div>hPDLSCs were subjected to shear stress at 0.5 and 5 dyn/cm², both with and without serum starvation. Cell viability and apoptosis were assessed using the Resazurin assay and flow cytometry analysis, respectively. Gene and protein expressions were analysed by real-time polymerase chain reaction, immunofluorescent staining, and Western blotting.</div></div><div><h3>Results</h3><div>Our results revealed that shear stress potentially mitigated serum derivation-induced cell death by inducing cell viability, enhancing colony formation, and inhibiting cell apoptosis. The addition of an ERK inhibitor inhibited the shear stress-induced cell apoptosis resistance. Shear stress treatment upregulated cell viability-related gene expression, including <em>SOX2</em>, <em>SOD1</em> and <em>BIRC5.</em> In particular, shear stress promoted the nuclear translocation of SOX2. Meanwhile, the expression of <em>BIRC5</em> was not inhibited by cycloheximide. Shear stress-induced <em>SOX2</em> and <em>BIRC5</em> expression was attenuated by PI3K and ERK inhibitors, respectively.</div></div><div><h3>Conclusions</h3><div>Shear stress contributes to promoting <em>SOX2</em> and <em>BIRC5</em> expression by hPDLSCs, implicating the promotion of stemness and cell survival under serum starvation.</div></div>\",\"PeriodicalId\":8288,\"journal\":{\"name\":\"Archives of oral biology\",\"volume\":\"173 \",\"pages\":\"Article 106232\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2025-03-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Archives of oral biology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0003996925000603\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"DENTISTRY, ORAL SURGERY & MEDICINE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Archives of oral biology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0003996925000603","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"DENTISTRY, ORAL SURGERY & MEDICINE","Score":null,"Total":0}
The study investigated in vitro the influences of shear stress preconditioning on human periodontal ligament stem cells (hPDLSCs) under serum deprivation.
Design
hPDLSCs were subjected to shear stress at 0.5 and 5 dyn/cm², both with and without serum starvation. Cell viability and apoptosis were assessed using the Resazurin assay and flow cytometry analysis, respectively. Gene and protein expressions were analysed by real-time polymerase chain reaction, immunofluorescent staining, and Western blotting.
Results
Our results revealed that shear stress potentially mitigated serum derivation-induced cell death by inducing cell viability, enhancing colony formation, and inhibiting cell apoptosis. The addition of an ERK inhibitor inhibited the shear stress-induced cell apoptosis resistance. Shear stress treatment upregulated cell viability-related gene expression, including SOX2, SOD1 and BIRC5. In particular, shear stress promoted the nuclear translocation of SOX2. Meanwhile, the expression of BIRC5 was not inhibited by cycloheximide. Shear stress-induced SOX2 and BIRC5 expression was attenuated by PI3K and ERK inhibitors, respectively.
Conclusions
Shear stress contributes to promoting SOX2 and BIRC5 expression by hPDLSCs, implicating the promotion of stemness and cell survival under serum starvation.
期刊介绍:
Archives of Oral Biology is an international journal which aims to publish papers of the highest scientific quality in the oral and craniofacial sciences. The journal is particularly interested in research which advances knowledge in the mechanisms of craniofacial development and disease, including:
Cell and molecular biology
Molecular genetics
Immunology
Pathogenesis
Cellular microbiology
Embryology
Syndromology
Forensic dentistry