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有和无矿化不全型釉质缺陷的龋损乳磨牙中牙本质细胞和成牙本质细胞的标记物和牙本质反应。

Odontoblast markers and dentine reactions in carious primary molars with and without hypomineralised enamel defects.

机构信息

Paediatric Dentistry, Melbourne Dental School, The University of Melbourne, Melbourne, Vic., Australia.

Oral Health Services, Health Care Agency, Mahé, Republic of Seychelles.

出版信息

Int J Paediatr Dent. 2021 Jul;31(4):451-458. doi: 10.1111/ipd.12750. Epub 2020 Dec 11.

Abstract

BACKGROUND

Wnt/β-Catenin signalling and DMP1 have key roles in tertiary dentinogenesis.

AIM

To compare the relationship between remaining dentine thickness (RDT), tertiary dentine thickness (TDT), β-catenin and dentine matrix protein 1 (DMP1) in carious second primary molar teeth with normal (SPM) and hypomineralised enamel (HSPM).

DESIGN

Extracted carious SPM and HSPM were fixed, sectioned (5 μm) and stained with haematoxylin and eosin or with indirect immunofluorescence for β-catenin and DMP1. Image analysis was performed to determine RDT, TDT, β-catenin and DMP1 intensity in the odontoblast layer and dentine-pulp complex.

RESULTS

Carious SPM (n = 11; mean RDT = 1536.1 μm) and HSPM (n = 12; mean RDT = 1179.9 μm) had mean TDT 248.6 μm and 518.1 μm, respectively (P = .02). There were no significant differences in intensity values in the odontoblast layer and dentine-pulp complex for β-catenin and DMP1 for both groups.

CONCLUSION

There was no observable variation in Wnt/β-catenin and DMP1 expression between HSPM and SPM despite a statistically significant twofold increased TDT in HSPM compared with SPM that had similar RDT. Thus, the observed increased TDT in HSPM is more likely due to an earlier onset of repair processes rather than an amplified response to caries.

摘要

背景

Wnt/β-连环蛋白信号和 DMP1 在第三期牙本质生成中具有关键作用。

目的

比较龋坏第二恒磨牙(SPM)和低矿化釉质(HSPM)中剩余牙本质厚度(RDT)、第三期牙本质厚度(TDT)、β-连环蛋白和牙本质基质蛋白 1(DMP1)之间的关系。

设计

固定提取的龋坏 SPM 和 HSPM,进行切片(5μm),并进行苏木精和曙红或间接免疫荧光染色,以检测β-连环蛋白和 DMP1。通过图像分析确定成牙本质细胞层和牙髓复合体中的 RDT、TDT、β-连环蛋白和 DMP1 强度。

结果

龋坏 SPM(n=11;平均 RDT=1536.1μm)和 HSPM(n=12;平均 RDT=1179.9μm)的平均 TDT 分别为 248.6μm 和 518.1μm(P=0.02)。两组的β-连环蛋白和 DMP1 在成牙本质细胞层和牙髓复合体中的强度值均无显著差异。

结论

尽管 HSPM 的 TDT 统计学上显著增加了两倍,但与 SPM 相比,其 RDT 相似,HSPM 中 Wnt/β-连环蛋白和 DMP1 的表达没有观察到明显变化。因此,HSPM 中观察到的 TDT 增加更可能是由于修复过程的早期开始,而不是对龋病的放大反应。

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