›› 2017, Vol. 8 ›› Issue (3): 132-135.

• 论著 • 上一篇    下一篇

Acvr1敲除对牙本质形成的影响研究

张雪1,刘麒麟2,李媛3,赵欢1,刘苍维4,闫广兴4,胡月1,李道伟1,史册1,孙宏晨1   

  1. 1. 吉林大学口腔医学院病理科
    2. 吉林大学口腔医院 口腔颌面外科
    3. 吉林大学口腔医院
    4. 吉林大学口腔医学院 口腔病理科
  • 收稿日期:2017-06-27 修回日期:2017-08-31 出版日期:2017-09-25 发布日期:2017-10-24
  • 通讯作者: 孙宏晨 E-mail:hcsun@mail.jlu.edu.cn
  • 基金资助:
    国家重点研发专项“新型颌面软硬组织修复材料研发”;国家自然科学基金国际(地区)合作与交流项目;国家自然科学基金青年基金项目;中国博士后科学基金

The role of BMP type I receptor ACVR1 in regulating dentin formation

  • Received:2017-06-27 Revised:2017-08-31 Online:2017-09-25 Published:2017-10-24

摘要: 目的:探讨牙乳头细胞中Ⅰ型骨形成蛋白受体——活化蛋白A受体1基因(ACVR1)敲除对牙本质形成的影响。方法:以同窝Osterix-Cre; Acvr1fx/-基因型小鼠为实验组,Osterix-Cre; Acvr1fx/+小鼠为对照组,利用影像学方法和HE染色初步观察Acvr1条件性基因敲除后小鼠牙本质形成及成牙本质细胞形态;免疫组织化学染色检测成牙/成骨分化相关蛋白水平;实时定量RT-PCR技术检测成牙/成骨分化相关因子的表达。结果:micro-CT显示,实验组下颌骨表现为疏松多孔样结构,磨牙牙本质变薄,前期牙本质增厚,HE染色显示成牙本质细胞排列紊乱,而切牙出现骨样牙本质;实验组磨牙成牙本质细胞分化相关基因Dspp、Nestin表达有下调趋势(无统计学差异),切牙成牙齿分化相关基因Dspp表达有下调趋势(无统计学差异),免疫组织化学染色显示实验组磨牙DSPP表达减少。结论:ACVR1通过调控成牙本质细胞分化而影响牙本质形成,在调控成牙本质细胞成牙转化过程中具有重要作用。

Abstract: Objective:To explore the effect of knockout of Acvr1(activin A receptor type 1) on the formation of dentin. Methods: Acvr1 conditional knockout mice model was constructed using Cre-loxP system. The genotype Osterix-Cre; Acvr1fx/- was chosen as the experiment group and the genotype Osterix-Cre; Acvr1fx/+ was chosen as the control group in littermate. We observed the dentin formation and odontoblast morphology by imageology and HE staining. And we checked the expression of the odontoblast/osteoblast markers by immunohistochemical staining. Finally the expression of odontoblast/osteoblast genes was detected by qRT-PCR. Results:The mandibles of the experiment group showed more pores, the dentin of mandibular first molar was thinner, pre-dentin was thicker, and odontoblast looked irregular. The genes important for odontoblast differentiation such as Dspp, Nestin were downregulated. However, the incisor showed osteodentin, and the Dspp was down-regulated. IHC showed down-regulated DSPP in cKO molar. Conclusions:ACVR1 affected the formation of dentin by up-regulating odontoblast differentiation, and also had important role in odontoblast transition.