{"title":"移植到正常和无菌动物体内修复牙本质形成。","authors":"T Inoue, M Shimono","doi":"","DOIUrl":null,"url":null,"abstract":"<p><strong>Unlabelled: </strong>The purpose of this study was to investigate the dentinogenesis of dental pulp tissue following transplantation and during regeneration in normal and germ free animals, as well as in vitro experiments.</p><p><strong>Experiments: </strong>(1) Partial and complete exposure of dental pulp in germ free rats by removing the enamel and dentin of molars. (2) The central portion of rat incisor which consisted of pulp and pulp chamber were autografted into various tissues. (3) Explants of rat pulp tissue were cultured on dentin matrix. (4) Resin bonding agent, 4-META/MMA-TBB-O (Superbond), was placed directly on surgically-exposed dental pulp.</p><p><strong>Results: </strong>(1) Dentin bridge formation was recognized at 5 days after operation in germ free rat. (2) The cut surface of the transplant exhibited dentin bridge at 7 days after implantation, and the thickness of the newly formed dentin increased gradually thereafter up to 30 days. (3) Cultured pulp cells had high alkaline phosphatase activity and bone- or dentin-like hard tissue was synthesized on the dentin matrix in vitro. (4) Dentin bridge formation was evident on the surgically-exposed dental pulp even after application of Superbond. From these results, it is suggested that pulp tissue has a high activity of dentinogenesis both in vivo and in vitro and 3 days is enough for pulp cells to express the odontoblast phenotype when inflammatory factors are not present.</p>","PeriodicalId":76355,"journal":{"name":"Proceedings of the Finnish Dental Society. Suomen Hammaslaakariseuran toimituksia","volume":"88 Suppl 1 ","pages":"183-94"},"PeriodicalIF":0.0000,"publicationDate":"1992-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Repair dentinogenesis following transplantation into normal and germ-free animals.\",\"authors\":\"T Inoue, M Shimono\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Unlabelled: </strong>The purpose of this study was to investigate the dentinogenesis of dental pulp tissue following transplantation and during regeneration in normal and germ free animals, as well as in vitro experiments.</p><p><strong>Experiments: </strong>(1) Partial and complete exposure of dental pulp in germ free rats by removing the enamel and dentin of molars. (2) The central portion of rat incisor which consisted of pulp and pulp chamber were autografted into various tissues. (3) Explants of rat pulp tissue were cultured on dentin matrix. (4) Resin bonding agent, 4-META/MMA-TBB-O (Superbond), was placed directly on surgically-exposed dental pulp.</p><p><strong>Results: </strong>(1) Dentin bridge formation was recognized at 5 days after operation in germ free rat. (2) The cut surface of the transplant exhibited dentin bridge at 7 days after implantation, and the thickness of the newly formed dentin increased gradually thereafter up to 30 days. (3) Cultured pulp cells had high alkaline phosphatase activity and bone- or dentin-like hard tissue was synthesized on the dentin matrix in vitro. (4) Dentin bridge formation was evident on the surgically-exposed dental pulp even after application of Superbond. From these results, it is suggested that pulp tissue has a high activity of dentinogenesis both in vivo and in vitro and 3 days is enough for pulp cells to express the odontoblast phenotype when inflammatory factors are not present.</p>\",\"PeriodicalId\":76355,\"journal\":{\"name\":\"Proceedings of the Finnish Dental Society. Suomen Hammaslaakariseuran toimituksia\",\"volume\":\"88 Suppl 1 \",\"pages\":\"183-94\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1992-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Proceedings of the Finnish Dental Society. Suomen Hammaslaakariseuran toimituksia\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Proceedings of the Finnish Dental Society. Suomen Hammaslaakariseuran toimituksia","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
未标记:本研究的目的是研究正常和无菌动物牙髓移植后和再生过程中牙本质组织的形成,以及体外实验。实验:(1)通过去除磨牙的牙釉质和牙本质,部分和完全暴露无菌大鼠的牙髓。(2)将大鼠切牙中央部分由牙髓和牙髓腔组成,自体移植到不同的组织中。(3)在牙本质基质上培养大鼠牙髓组织。(4)将树脂粘接剂4- meta /MMA-TBB-O (Superbond)直接放置在手术暴露的牙髓上。结果:(1)无菌大鼠术后5 d牙本质桥形成。(2)移植体的切口表面在种植后第7天出现牙本质桥,此后至第30天新形成的牙本质厚度逐渐增加。(3)培养的牙髓细胞具有较高的碱性磷酸酶活性,在体外牙本质基质上合成了骨或牙本质样硬组织。(4)应用Superbond后,牙本质桥的形成在手术暴露的牙髓上仍很明显。这些结果表明,牙髓组织在体内和体外都具有较高的牙本质形成活性,在没有炎症因子存在的情况下,3天足够牙髓细胞表达成牙本质表型。
Repair dentinogenesis following transplantation into normal and germ-free animals.
Unlabelled: The purpose of this study was to investigate the dentinogenesis of dental pulp tissue following transplantation and during regeneration in normal and germ free animals, as well as in vitro experiments.
Experiments: (1) Partial and complete exposure of dental pulp in germ free rats by removing the enamel and dentin of molars. (2) The central portion of rat incisor which consisted of pulp and pulp chamber were autografted into various tissues. (3) Explants of rat pulp tissue were cultured on dentin matrix. (4) Resin bonding agent, 4-META/MMA-TBB-O (Superbond), was placed directly on surgically-exposed dental pulp.
Results: (1) Dentin bridge formation was recognized at 5 days after operation in germ free rat. (2) The cut surface of the transplant exhibited dentin bridge at 7 days after implantation, and the thickness of the newly formed dentin increased gradually thereafter up to 30 days. (3) Cultured pulp cells had high alkaline phosphatase activity and bone- or dentin-like hard tissue was synthesized on the dentin matrix in vitro. (4) Dentin bridge formation was evident on the surgically-exposed dental pulp even after application of Superbond. From these results, it is suggested that pulp tissue has a high activity of dentinogenesis both in vivo and in vitro and 3 days is enough for pulp cells to express the odontoblast phenotype when inflammatory factors are not present.