Huihui Ren , Qingxuan Zhao , Nan Wang , Xiaojing Yuan , Rui Song , Quan Wen , Yuming Zhao
{"title":"黑色素瘤抑制活性可促进根尖乳头干细胞的迁移和牙骨质分化。","authors":"Huihui Ren , Qingxuan Zhao , Nan Wang , Xiaojing Yuan , Rui Song , Quan Wen , Yuming Zhao","doi":"10.1016/j.archoralbio.2024.106109","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><div>Melanoma Inhibitory Activity (MIA) has been predominantly studied in the context of melanoma and cartilage development. However, its role in dental pulp development and stem cell behavior remains largely unexplored. This study investigates the expression pattern of MIA in dental pulp tissues and its potential role in the proliferation, migration, and odontoblastic differentiation of stem cells from the apical papilla (SCAPs).</div></div><div><h3>Design</h3><div>MIA expression in human pulp tissue was demonstrated by immunohistochemistry. SCAPs were cultured in normal and mineralization induction media, with MIA levels monitored via RT-qPCR and Western blot. Cell proliferation was evaluated using the CCK8 assay, while transwell and cell scratch assays were conducted to examine cell migration. The effect of MIA on odontoblastic differentiation was examined by qRT-PCR, Alkaline phosphatase activity assay, and Western blot. siRNA was used to knock down MIA to investigate its effect. A mouse subcutaneous implantation model was used to assess whether MIA promotes odontoblastic differentiation <em>in vivo</em>.</div></div><div><h3>Results</h3><div>MIA expression was observed in the papilla and odontoblasts layer of the developing pulp. <em>In vitro</em>, MIA expression increased during SCAPs differentiation and was found to significantly enhance migration, and odontoblastic differentiation but not proliferation. Gene knockdown experiments confirmed MIA’s pivotal role in promoting SCAPs migration and differentiation. <em>In vivo</em>, MIA facilitated the formation of dentin-like structures and enhanced pulp-dentin complex regeneration.</div></div><div><h3>Conclusion</h3><div>MIA plays a crucial role in SCAPs’ migration and differentiation, suggesting its potential application in pulp-dentin regeneration therapies. Further studies are required to fully elucidate the underlying mechanisms.</div></div>","PeriodicalId":8288,"journal":{"name":"Archives of oral biology","volume":"169 ","pages":"Article 106109"},"PeriodicalIF":2.2000,"publicationDate":"2024-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Melanoma-inhibiting activity promotes the migration and odontoblastic differentiation of stem cells of apical papilla\",\"authors\":\"Huihui Ren , Qingxuan Zhao , Nan Wang , Xiaojing Yuan , Rui Song , Quan Wen , Yuming Zhao\",\"doi\":\"10.1016/j.archoralbio.2024.106109\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Objective</h3><div>Melanoma Inhibitory Activity (MIA) has been predominantly studied in the context of melanoma and cartilage development. However, its role in dental pulp development and stem cell behavior remains largely unexplored. This study investigates the expression pattern of MIA in dental pulp tissues and its potential role in the proliferation, migration, and odontoblastic differentiation of stem cells from the apical papilla (SCAPs).</div></div><div><h3>Design</h3><div>MIA expression in human pulp tissue was demonstrated by immunohistochemistry. SCAPs were cultured in normal and mineralization induction media, with MIA levels monitored via RT-qPCR and Western blot. Cell proliferation was evaluated using the CCK8 assay, while transwell and cell scratch assays were conducted to examine cell migration. The effect of MIA on odontoblastic differentiation was examined by qRT-PCR, Alkaline phosphatase activity assay, and Western blot. siRNA was used to knock down MIA to investigate its effect. A mouse subcutaneous implantation model was used to assess whether MIA promotes odontoblastic differentiation <em>in vivo</em>.</div></div><div><h3>Results</h3><div>MIA expression was observed in the papilla and odontoblasts layer of the developing pulp. <em>In vitro</em>, MIA expression increased during SCAPs differentiation and was found to significantly enhance migration, and odontoblastic differentiation but not proliferation. Gene knockdown experiments confirmed MIA’s pivotal role in promoting SCAPs migration and differentiation. <em>In vivo</em>, MIA facilitated the formation of dentin-like structures and enhanced pulp-dentin complex regeneration.</div></div><div><h3>Conclusion</h3><div>MIA plays a crucial role in SCAPs’ migration and differentiation, suggesting its potential application in pulp-dentin regeneration therapies. Further studies are required to fully elucidate the underlying mechanisms.</div></div>\",\"PeriodicalId\":8288,\"journal\":{\"name\":\"Archives of oral biology\",\"volume\":\"169 \",\"pages\":\"Article 106109\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2024-10-16\",\"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/S0003996924002309\",\"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/S0003996924002309","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}
引用次数: 0
摘要
目的:黑色素瘤抑制活性(MIA)主要是在黑色素瘤和软骨发育的背景下进行研究的。然而,它在牙髓发育和干细胞行为中的作用在很大程度上仍未得到探索。本研究调查了MIA在牙髓组织中的表达模式及其在牙髓根尖乳头干细胞(SCAPs)的增殖、迁移和牙髓分化中的潜在作用:设计:通过免疫组化方法证实 MIA 在人类牙髓组织中的表达。在正常培养基和矿化诱导培养基中培养SCAPs,通过RT-qPCR和Western印迹监测MIA水平。细胞增殖采用 CCK8 试验进行评估,细胞迁移则采用跨孔试验和细胞划痕试验进行检测。通过 qRT-PCR、碱性磷酸酶活性检测和 Western 印迹检测了 MIA 对骨骺分化的影响。用小鼠皮下植入模型评估MIA是否促进了体内颌骨的分化:结果:在发育中的牙髓乳头和牙本质层观察到了MIA的表达。在体外,MIA的表达在SCAPs分化过程中增加,并被发现能显著促进迁移和牙本质分化,但不能促进增殖。基因敲除实验证实了 MIA 在促进 SCAPs 迁移和分化中的关键作用。在体内,MIA 促进了牙本质样结构的形成,并增强了牙髓-牙本质复合体的再生能力:结论:MIA 在 SCAPs 的迁移和分化中起着关键作用,这表明它有可能应用于牙髓-牙本质再生疗法。结论:MIA 对 SCAPs 的迁移和分化起着关键作用,这表明它有可能应用于牙髓-牙本质再生疗法。
Melanoma-inhibiting activity promotes the migration and odontoblastic differentiation of stem cells of apical papilla
Objective
Melanoma Inhibitory Activity (MIA) has been predominantly studied in the context of melanoma and cartilage development. However, its role in dental pulp development and stem cell behavior remains largely unexplored. This study investigates the expression pattern of MIA in dental pulp tissues and its potential role in the proliferation, migration, and odontoblastic differentiation of stem cells from the apical papilla (SCAPs).
Design
MIA expression in human pulp tissue was demonstrated by immunohistochemistry. SCAPs were cultured in normal and mineralization induction media, with MIA levels monitored via RT-qPCR and Western blot. Cell proliferation was evaluated using the CCK8 assay, while transwell and cell scratch assays were conducted to examine cell migration. The effect of MIA on odontoblastic differentiation was examined by qRT-PCR, Alkaline phosphatase activity assay, and Western blot. siRNA was used to knock down MIA to investigate its effect. A mouse subcutaneous implantation model was used to assess whether MIA promotes odontoblastic differentiation in vivo.
Results
MIA expression was observed in the papilla and odontoblasts layer of the developing pulp. In vitro, MIA expression increased during SCAPs differentiation and was found to significantly enhance migration, and odontoblastic differentiation but not proliferation. Gene knockdown experiments confirmed MIA’s pivotal role in promoting SCAPs migration and differentiation. In vivo, MIA facilitated the formation of dentin-like structures and enhanced pulp-dentin complex regeneration.
Conclusion
MIA plays a crucial role in SCAPs’ migration and differentiation, suggesting its potential application in pulp-dentin regeneration therapies. Further studies are required to fully elucidate the underlying mechanisms.
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