KLF4 和 KLF5 在小鼠牙齿发育过程中的时空表达。

Spatial and temporal expression of KLF4 and KLF5 during murine tooth development.

机构信息

Key Laboratory for Oral Biomedical Engineering of Ministry of Education, School and Hospital of Stomatology, Wuhan University, Wuhan, Hubei 430079, PR China.

出版信息

Arch Oral Biol. 2009 May;54(5):403-11. doi: 10.1016/j.archoralbio.2009.02.003. Epub 2009 Mar 6.

Abstract

OBJECTIVE

KLF4 and KLF5, members of the Krüppel-like factor (KLF) family, play key roles in proliferation, differentiation and apoptosis during development. In order to determine if these transcription factors are associated with tooth development, we examined the expression pattern of KLF4 and KLF5 during murine tooth development.

DESIGN

In situ hybridization and immunohistochemistry were performed to detect the expression pattern of KLF4 and KLF5 from E12.5 to PN3 during murine tooth development.

RESULTS

In situ hybridization analysis revealed that Klf4 was specifically expressed in polarizing odontoblasts from E16.5 (incisor) or E18.5 (first molar) to PN3. Immunohistochemistry staining showed that KLF4 was specifically expressed in both polarizing odontoblasts and ameloblasts at the same stages. KLF5 was mainly expressed from E18.5 to PN3 in secretory ameloblasts when enamel mineralization occurs and in secretory odontoblasts. However, an expression of KLF5 was also observed at earlier stages (E14.5 and E16.5) mainly in proliferating epithelial cells.

CONCLUSIONS

These results suggest that the expression of KLF4 is closely correlated to the growth-arrest and the first step of odontoblast and ameloblast differentiation. Furthermore, KLF5 maybe involved in proliferation at the early stages of tooth development and related to mineralization of both enamel and dentin matrices at later stages.

摘要

目的

Krüppel 样因子(KLF)家族的成员 KLF4 和 KLF5 在发育过程中的增殖、分化和凋亡中发挥关键作用。为了确定这些转录因子是否与牙齿发育有关,我们研究了 KLF4 和 KLF5 在小鼠牙齿发育过程中的表达模式。

设计

在原位杂交和免疫组织化学检测中,检测了 KLF4 和 KLF5 在小鼠牙齿发育过程中从 E12.5 到 PN3 的表达模式。

结果

原位杂交分析显示,Klf4 特异性表达于从 E16.5(切牙)或 E18.5(第一磨牙)到 PN3 的极化成牙本质细胞中。免疫组织化学染色显示,KLF4 特异性表达于同一阶段的极化成牙本质细胞和成釉细胞中。KLF5 主要在 E18.5 到 PN3 的分泌期成釉细胞中表达,此时牙釉质发生矿化,也在分泌期成牙本质细胞中表达。然而,在早期阶段(E14.5 和 E16.5)也观察到 KLF5 的表达,主要在增殖的上皮细胞中。

结论

这些结果表明,KLF4 的表达与成牙本质细胞的生长停滞和第一阶段分化密切相关。此外,KLF5 可能参与牙齿发育早期的增殖,并与牙釉质和牙本质基质的矿化有关。

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