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Dentinogenesis and Tooth-Alveolar Bone Complex Defects in BMP9/GDF2 Knockout Mice

机译:BMP9 / GDF2敲除小鼠中的牙本发生和牙齿肺泡骨复杂缺陷

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摘要

Tooth development is regulated by sequential and reciprocal epithelium-mesenchymal interactions and their related molecular signaling pathways, such as bone morphogenetic proteins (BMPs). Among the 14 types of BMPs, BMP9 (also known as growth differentiation factor 2) is one of the most potent BMPs to induce osteogenic differentiation of mesenchymal stem cells. The purpose of this study was to examine potential roles of BMP9 signaling in tooth development. First, we detected the expression pattern of BMP9 in tooth germ during postnatal tooth development, and we found that BMP9 was widely expressed in odontoblasts, ameloblasts, dental pulp cells, and osteoblasts in alveolar bones. Then, we established a BMP9-KO mouse model. Gross morphological examination revealed that the tooth cusps of BMP9-KO mice were significantly abraded with shorter roots. Micro-computed tomography and three-dimensional reconstruction analysis indicated that the first molars of the BMP9-KO mice exhibited a reduced thickness dentin, enlarged pulp canals, and shortened roots, resembling the phenotypes of the common hereditary dental disease dentinogenesis imperfecta. Further, the alveolar bone of the BMP9-KO mutants was found to be shorter and had a decreased mineral density and trabecular thickness and bone volume fraction compared with that of the wild-type control. Mechanistically, we demonstrated that both dentin sialophosphoprotein and dentin matrix protein 1 were induced in dental stem cells by BMP9, whereas their expression was reduced when BMP9 was silenced. Further studies are required to determine whether loss of or decreased BMP9 expression is clinically associated with dentinogenesis imperfecta. Collectively, our results strongly suggest that BMP9 may play an important role in regulating dentinogenesis and tooth development. Further research is recommended into the therapeutic uses of BMP9 to regenerate traumatized and diseased tissues and for the bioengineering of replacement teeth.
机译:通过顺序和互易上皮 - 间充质相互作用及其相关分子信号传导途径(如骨形态发生蛋白(BMP))调节牙齿发育。在14种类型的BMP中,BMP9(也称为生长分化因子2)是最有效的BMP之一,以诱导间充质干细胞的成骨分化。本研究的目的是检查BMP9信号传导在牙齿发育中的潜在作用。首先,我们在出生牙齿发育期间检测到牙胚中BMP9的表达模式,我们发现BMP9广泛表达在牙槽骨中的Odontoblasts,Ameloblasts,牙科纸浆细胞和成骨细胞中。然后,我们建立了BMP9-KO鼠标模型。总体形态学检查显示,BMP9-KO小鼠的牙齿尖端显着磨损,较短的根。微计算断层扫描和三维重建分析表明,第一个臼齿的BMP9-KO小鼠表现出厚度牙本质,扩大的纸浆运河和缩小根部,类似于常见的遗传性牙科疾病的表型牙本质生殖器牙型缺乏细胞。此外,发现BMP9-KO突变体的肺泡骨骼更短,与野生型对照相比,矿物质密度和骨质厚度和骨体积分数的降低。机械地,我们证明了BMP9在牙科干细胞中诱导了牙本质唾液酸磷蛋白和牙本质基质蛋白1,而当BMP9静音时,它们的表达降低。需要进一步的研究来确定BMP9表达的丧失或降低是否与牙本质生成不完全相关。统称,我们的结果强烈表明BMP9可能在调节牙本发生和牙齿发育方面发挥重要作用。建议进一步研究BMP9的治疗用途,以再生创伤和患病组织和替代牙齿的生物工程。

著录项

  • 来源
    《Stem cells and development》 |2019年第10期|共12页
  • 作者单位

    Chongqing Med Univ Affiliated Hosp Stomatol Chongqing Key Lab Oral Dis &

    Biomed Sci Chongqing;

    Chongqing Med Univ Affiliated Stomatol Hosp Dept Pediat Dent Chongqing Peoples R China;

    Chongqing Med Univ Affiliated Hosp 1 Dept Orthoped Surg Chongqing Peoples R China;

    Chongqing Med Univ Affiliated Hosp Stomatol Chongqing Key Lab Oral Dis &

    Biomed Sci Chongqing;

    Chongqing Med Univ Affiliated Hosp Stomatol Chongqing Key Lab Oral Dis &

    Biomed Sci Chongqing;

    Chongqing Med Univ Affiliated Hosp Stomatol Chongqing Key Lab Oral Dis &

    Biomed Sci Chongqing;

    Chongqing Med Univ Affiliated Hosp Stomatol Chongqing Key Lab Oral Dis &

    Biomed Sci Chongqing;

    Chongqing Med Univ Affiliated Hosp Stomatol Chongqing Key Lab Oral Dis &

    Biomed Sci Chongqing;

    Chongqing Med Univ Affiliated Hosp Stomatol Chongqing Key Lab Oral Dis &

    Biomed Sci Chongqing;

    Chongqing Med Univ Affiliated Hosp Stomatol Chongqing Key Lab Oral Dis &

    Biomed Sci Chongqing;

    Chongqing Med Univ Affiliated Hosp Stomatol Chongqing Key Lab Oral Dis &

    Biomed Sci Chongqing;

    Chongqing Med Univ Affiliated Hosp Stomatol Chongqing Key Lab Oral Dis &

    Biomed Sci Chongqing;

    Chongqing Med Univ Minist Educ Key Lab Diagnost Med Chongqing Peoples R China;

    Chongqing Med Univ Affiliated Hosp 1 Dept Orthoped Surg Chongqing Peoples R China;

    Chongqing Med Univ Affiliated Hosp 2 Dept Orthopaed Surg Chongqing Peoples R China;

    Chongqing Med Univ Affiliated Hosp Stomatol Chongqing Key Lab Oral Dis &

    Biomed Sci Chongqing;

    Chongqing Med Univ Affiliated Hosp Stomatol Chongqing Key Lab Oral Dis &

    Biomed Sci Chongqing;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 基础医学;
  • 关键词

    bone morphogenetic protein 9; dentinogenesis; tooth development; dental stem cells; odontoblastic differentiation; dentinogenesis imperfecta;

    机译:骨形态发生蛋白9;牙本发生;牙齿发育;牙科干细胞;Odontobolas弹性分化;牙本生成不完全;

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