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Immunolocalization of gene products responsible for amelogensis imperfecta and dentinogenesis imperfecta in mice

机译:小鼠阿米洛不全和牙本质生成不全的基因产物的免疫定位

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摘要

Healthy tooth formation is crucially dependent on normal development of enamel and dentin. Any deviation from norm could lead to serious effects on the teeth function.;Amelogensis Imperfecta (AI) and Dentinogensis Imperfecta (DGI) are genetically inherited conditions that affect the teeth formation. Thus is imperative to investigate the genes and proteins that contribute to these conditions. Some of the known proteins that play a role in amelogenesis include AMELOGENIN (AMLEX), KALLIKREIN 4(KLK4), FAMILY WITH SEQUENCE SIMILARITY 83H (FAM83H), WD REPEAT-CONTAINING PROTEIN 72 (WDR72) and DENTIN SIALOPHSOPHPROTEIN (DSPP).;The purpose of this research project was to investigate the expression/localization pattern of gene products which are known to be causative for Amelogensis Imperfecta and Dentinogensis Imperfecta. The study was carried out using mouse heads which were fixed, demineralized and paraffin-embedded. Samples were then sectioned and immunohistochemical analysis was performed with various enamel/dentin protein antibodies.;The data showed the following results: KLK4 showed immunoreactivity mainly in ameloblasts and in the pulp, DSPP showed immunoreactivity in dentin, in the pulp and in the epithelial cells on one location as indicated by the arrow in figure 3 of the tooth cross section, FAM83H has a faint immunoreactivity identified in the ameloblasts, WDR72 showed weak immunoreactivity in the ameloblasts and AMELX showed immunoreactivity on the enamel and the ameloblasts.;In conclusion these findings were supported by previous studies and conveyed the validity of IHC experiments in locating these proteins in odontogenic tissues.
机译:健康的牙齿形成至关重要地取决于牙釉质和牙本质的正常发育。任何偏离规范的行为都会严重影响牙齿的功能。;阿米洛不完善(AI)和牙本质不完整(DGI)是遗传性疾病,会影响牙齿的形成。因此,必须研究有助于这些条件的基因和蛋白质。 ;一些已知的在牙釉质形成中起作用的蛋白质包括AMELOGENIN(AMLEX),KALLIKREIN 4(KLK4),具有序列相似性83H(FAM83H)的家族,WD REPEAT-CONTAINING Protein 72(WDR72)和DENTIN SIALOPHSOPHPROTEIN(DSPP)。该研究项目的目的是研究已知对Amelogensis Imperfecta和Dentinogensis Imperfecta有致病性的基因产物的表达/定位模式。该研究是使用固定,去矿质和石蜡包埋的小鼠头部进行的。然后将样品切片并用各种牙釉质/牙本质蛋白抗体进行免疫组化分析;数据显示以下结果:KLK4主要在成釉细胞和牙髓中显示免疫反应性,DSPP在牙本质,牙髓和上皮细胞中显示免疫反应性在牙齿横截面图3中箭头所示的一个位置上,FAM83H在成釉细胞中鉴定出微弱的免疫反应性,WDR72在成釉细胞中显示出弱的免疫反应性,而AMELX在釉质和成釉细胞上显示出免疫反应性。得到先前研究的支持,并传达了IHC实验在牙源性组织中定位这些蛋白质的有效性。

著录项

  • 作者

    Alkhouly, Waddah M.;

  • 作者单位

    Boston University.;

  • 授予单位 Boston University.;
  • 学科 Molecular biology.
  • 学位 M.S.D.
  • 年度 2016
  • 页码 60 p.
  • 总页数 60
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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