《Journal of Oral and Maxillofacial Surgery》

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The Osteogenesis and Cementogenic Capacities of Gli1+ Cells in Periodontal Membrane

LIU An-qi, ZHANG Li-shu, CHEN Ji, JIN Yan, HU Cheng-hu   

  1. 1. State Key Laboratory of Military Stomatology and National Clinical Research Center for Oral Diseases, Shaanxi International Joint Research Center for Oral Diseases, Department of Pathology, School of Stomatology, The Fourth Military Medical University, Xi'an 710061; 2. Xi'an Institute of Tissue Engineering and Regenerative Medicine, Xi'an 710032, Shaanxi Province, China
  • Online:2019-12-28 Published:2019-12-25

牙周膜中Gli1阳性细胞的成骨及成牙骨质能力研究

刘安琪,张立书,陈骥,金岩,胡成虎   

  1. 1. 军事口腔医学国家重点实验室,国家口腔疾病临床医学研究中心,陕西省口腔疾病国际联合研究中心,第四军医 大学口腔医院组织病理学教研室,陕西 西安 710061;2. 西安组织工程与再生医学研究所,陕西 西安 710032
  • 通讯作者: 胡成虎,副研究员. E-mail: chenghu@xiterm.com E-mail:chenghu@xiterm.com
  • 作者简介:刘安琪(1991—),女,安徽六安人,博士研究生. E-mail: 854282800@qq.com
  • 基金资助:
    国家自然科学基金重点项目(81930025)

Abstract: Objective: To investigate the osteogenesis and cementogenic capacities of Gli1+ cells in periodontal membrane. Methods: This study utilized Gli1-CreERT2 mice with B6.129(Cg)-Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/J mice to generate Gli1-mT/mG mice which specific label Gli1+ cells after tamoxifen treatment. Furthermore, immunofluorescent staining was applied to detect the co-localization of Gli1+ cells with Runx2 (runt-related transcription factor 2) or CAP (cementum attachment protein). Results: This study successfully established the Gli1-mT/mG mice with EGFP protein expression in Gli1 positive cells. In addition, Gli1+ cells were widely expressed in periodontal tissue, and most of them expressed Runx2 and CAP protein. Conclusions: Gli1+ cells were widely expressed in periodontal tissue and probably participated in the process of periodontal physiologic remodeling.

Key words: Gli1+ cells, stem cells, mT/mG mice, periodontal tissue

摘要: 目的:研究牙周膜中的Gli1阳性(Gli1+)细胞的成骨及成牙骨质能力。方法:通过构建特异性表达Gli1的转基因小鼠,观察Gli1阳性细胞在牙周组织中的分布情况,应用免疫荧光染色观察Gli1阳性细胞与runt相关转录因子2(runt-related transcription factor 2,Runx2)和牙骨质附着蛋白(cementum attachment protein,CAP)的共定位情况。结果:成功构建特异性表达Gli1的双基因型小鼠,并观察到Gli1阳性细胞在牙周膜中广泛表达,且大部分均表达Runx2和CAP。结论:Gli1阳性细胞在牙周膜中广泛表达,可能参与了牙周组织的成骨和成牙骨质等生理性改建过程。

关键词: Gli1阳性细胞, 干细胞, mT/mG小鼠, 牙周组织

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