Ruspita Intan, Das Pragnya, Kelangi Sarah, Harvey Richard P, Bei Marianna
Center for Regenerative and Developmental Biology, The Forsyth Institute, Cambridge, USA.
Universitas Gadjah Mada, Yogyakarta, Indonesia.
Ann Pediatr Child Health. 2025;13(1). doi: 10.47739/pediatrics.1347. Epub 2025 Jan 29.
The gene belongs to the NK2 class of homeobox genes that play important role in vertebrate development and share overlapping expression patterns. are involved in several pathways that lead to cell differentiation, migration, and maturation of the cells, indicating their essential role in the formation and homeostasis of the organism. Here we report that the mouse mutants have an orofacial phenotype affecting among other structures and the developing teeth. Specifically, we confirm that while incisors and upper molars are normal, the mandibular molars of the mutants have abnormal crown shape. Second, we provide for the first time evidence that the absence of affects the differentiation process of the two most essential dental cell populations, namely the ameloblasts and the odontoblasts. Macroscopic, histological, 3D micro-CT of the lower molars of mouse mutants exhibit enamel and dentin phenotypes with the expression of the and genes to be selectively reduced in deficient secretory ameloblasts and dentinoblasts, respectively.
该基因属于同源盒基因的NK2类,在脊椎动物发育中起重要作用,并具有重叠的表达模式。它参与了导致细胞分化、迁移和成熟的多种途径,表明其在生物体形成和体内平衡中的重要作用。在这里我们报告,该小鼠突变体具有口面部表型,影响其他结构和正在发育的牙齿。具体而言,我们证实,虽然门牙和上颌磨牙正常,但突变体的下颌磨牙冠形状异常。其次,我们首次提供证据表明,该基因的缺失影响了两个最基本的牙细胞群体,即成釉细胞和成牙本质细胞的分化过程。对该小鼠突变体下颌磨牙进行宏观、组织学、三维显微CT检查,发现釉质和牙本质表型,且该基因和另一基因的表达分别在该基因缺陷的分泌性成釉细胞和成牙本质细胞中选择性降低。