Nkx2-3同源盒基因在口腔面部分化后期发挥重要作用

Annals of pediatrics & child health Pub Date : 2025-01-01 Epub Date: 2025-01-29 DOI:10.47739/pediatrics.1347
Intan Ruspita, Pragnya Das, Sarah Kelangi, Richard P Harvey, Marianna Bei
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引用次数: 0

摘要

Nkx2-3基因属于NK2类同源盒基因,在脊椎动物发育中起重要作用,具有重叠的表达模式。NK2s参与了导致细胞分化、迁移和成熟的几个途径,表明它们在生物体的形成和稳态中起着重要作用。在这里,我们报告了Nkx2-3lacZ∆HD/lacZ∆HD小鼠突变体具有影响其他结构和发育中的牙齿的口面部表型。具体来说,我们证实,虽然门牙和上磨牙是正常的,但突变体的下颌磨牙有异常的冠形。其次,我们首次提供证据表明,Nkx2-3的缺失会影响两种最重要的牙细胞群,即成釉细胞和成牙细胞的分化过程。Nkx2-3lacZDHD/lacZDHD小鼠突变体的下磨牙的宏观、组织学和3D显微ct显示,在Nkx2-3缺陷的分泌性成釉细胞和成牙本质细胞中,釉素(Enam)和牙本质唾液蛋白(DSPP)基因的表达分别选择性降低,从而表现出牙釉质和牙本质表型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nkx2-3 Homeobox Gene Plays an Essential Role in Later Stages of Orofacial Differentiation.

The Nkx2-3 gene belongs to the NK2 class of homeobox genes that play important role in vertebrate development and share overlapping expression patterns. NK2s 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 Nkx2-3lacZ∆HD/lacZ∆HD 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 Nkx2-3 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 Nkx2-3lacZDHD/lacZDHD mouse mutants exhibit enamel and dentin phenotypes with the expression of the Enamelin (Enam) and Dentin Sialophosphoprotein (DSPP) genes to be selectively reduced in Nkx2-3 deficient secretory ameloblasts and dentinoblasts, respectively.

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