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预成膜:揭示牙齿发育中未被探索的方面。

Membrana preformativa: Unveiling the unexplored facets of dental development.

作者信息

Sikaria Sakshi, Selvam Suganya Panneer, Ramadoss Ramya, Sundar Sandhya

机构信息

Department of Oral Biology, Saveetha Dental College and Hospital, Saveetha Institute of Medical and Technical Sciences, Chennai, 600077, India.

出版信息

J Oral Biol Craniofac Res. 2025 Jan-Feb;15(1):84-87. doi: 10.1016/j.jobcr.2024.12.010. Epub 2024 Dec 21.


DOI:10.1016/j.jobcr.2024.12.010
PMID:39810838
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11731231/
Abstract

AIM: Odontogenesis is a complex and highly regulated biological process that involves a range of molecular mechanisms. Among these, Ki67 and Cyclin D1 are crucial cell cycle regulators that play pivotal roles in controlling cell proliferation during tooth development. This study aims to provide detailed insights into the expression patterns and functional significance of Ki67 and Cyclin D1 in tooth development. Through rigorous analysis, we seek to elucidate the intricate mechanisms underlying tooth development, helping to advance our understanding of this vital biological process. MATERIALS & METHODS: The procurement of rabbit tooth germ was performed only after obtaining the requisite ethical clearance. Subsequently, the tissues were processed and subjected to Hematoxylin and Eosin staining to facilitate enhanced visualization of the overall tissue architecture and organization & immunohistochemical staining of Ki-67 and Cyclin D1 was performed. RESULTS: In the tooth germ, cyclin D1 demonstrated intense staining in the dental papilla, especially in the membrana preformativa, with this intensity decreasing following predentin formation. Odontoblasts showed mild staining as they transitioned from pre-odontoblasts, which further diminished after dentin formation. Both the dental papilla and differentiating odontoblasts were positive for Ki67, though Ki67 staining in the odontoblasts reduced after dentin formation. CONCLUSION: In conclusion, the membrana preformativa plays a key role in odontogenesis, as indicated by its involvement in cellular proliferation and differentiation during tooth development.

摘要

目的:牙发生是一个复杂且受到高度调控的生物学过程,涉及一系列分子机制。其中,Ki67和细胞周期蛋白D1是关键的细胞周期调节因子,在牙齿发育过程中控制细胞增殖方面发挥着关键作用。本研究旨在深入了解Ki67和细胞周期蛋白D1在牙齿发育中的表达模式和功能意义。通过严谨分析,我们试图阐明牙齿发育背后的复杂机制,以增进我们对这一重要生物学过程的理解。 材料与方法:仅在获得必要的伦理许可后才进行兔牙胚的获取。随后,对组织进行处理并进行苏木精和伊红染色,以更清晰地观察整体组织结构,同时对Ki-67和细胞周期蛋白D1进行免疫组织化学染色。 结果:在牙胚中,细胞周期蛋白D1在牙乳头中显示出强烈染色,尤其是在牙本质形成前期的成釉器中,随着前期牙本质形成,这种染色强度降低。成牙本质细胞从前期成牙本质细胞转变时显示出轻度染色,在牙本质形成后进一步减弱。牙乳头和正在分化的成牙本质细胞Ki67均呈阳性,不过成牙本质细胞中的Ki67染色在牙本质形成后减少。 结论:总之,成釉器在牙发生中起关键作用,这体现在其在牙齿发育过程中参与细胞增殖和分化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbc8/11731231/016cb0c3950c/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbc8/11731231/7b6202f0c731/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbc8/11731231/016cb0c3950c/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbc8/11731231/7b6202f0c731/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbc8/11731231/016cb0c3950c/gr2.jpg

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[1]
Membrana preformativa: Unveiling the unexplored facets of dental development.

J Oral Biol Craniofac Res. 2025

[2]
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[4]
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[8]
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[10]
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本文引用的文献

[1]
Bone or Tooth dentin: The TGF-β signaling is the key.

Int J Biol Sci. 2024

[2]
D-Type Cyclins in Development and Disease.

Genes (Basel). 2023-7-14

[3]
BMP Signaling Pathway in Dentin Development and Diseases.

Cells. 2022-7-16

[4]
The BMP and FGF pathways reciprocally regulate odontoblast differentiation.

Connect Tissue Res. 2023-1

[5]
Malignant odontogenic tumors: epigenetics in disease and therapy.

Acta Odontol Scand. 2023-1

[6]
PCNA and Ki67: Prognostic proliferation markers for oral cancer.

Oral Oncol. 2022-7

[7]
Partial epithelial-mesenchymal transition during enamel development.

Clin Exp Dent Res. 2022-4

[8]
MSX1 Drives Tooth Morphogenesis Through Controlling Wnt Signaling Activity.

J Dent Res. 2022-7

[9]
To form and function: on the role of basement membrane mechanics in tissue development, homeostasis and disease.

Open Biol. 2021-2

[10]
Laminin-Modified Dental Pulp Extracellular Matrix for Dental Pulp Regeneration.

Front Bioeng Biotechnol. 2021-1-13

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