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用于牙本质研究的动物模型及相关技术。

Animal models and related techniques for dentin study.

作者信息

Wang Shuai, Tu Yan, Yu Hao, Li Zhen, Feng Jinqiu, Liu Shangfeng

机构信息

Shanghai Key Laboratory of Craniomaxillofacial Development and Diseases, Shanghai Stomatological Hospital, Fudan University, 365 Beijing Road, Shanghai, 200001, People's Republic of China.

Department of Pediatrics, Shanghai Stomatological Hospital, Fudan University, Shanghai, 200001, People's Republic of China.

出版信息

Odontology. 2025 Jan;113(1):42-60. doi: 10.1007/s10266-024-00987-1. Epub 2024 Sep 3.

DOI:10.1007/s10266-024-00987-1
PMID:39225758
Abstract

The intricate and protracted process of dentin formation has been extensively explored, thanks to the significant advancements facilitated by the use of animal models and related techniques. Despite variations in their effectiveness, taking into account factors such as sensitivity, visibility, and reliability, these models or techniques are indispensable tools for investigating the complexities of dentin formation. This article focuses on the latest advances in animal models and related technologies, shedding light on the key molecular mechanisms that are essential in dentin formation. A deeper understanding of this phenomenon enables the careful selection of appropriate animal models, considering their suitability in unraveling the underlying molecular intricacies. These insights are crucial for the advancement of clinical drugs targeting dentin-related ailments and the development of comprehensive treatment strategies throughout the duration of the disease.

摘要

由于使用动物模型及相关技术带来了重大进展,牙本质形成这一复杂而漫长的过程已得到广泛研究。尽管这些模型或技术在敏感性、可视性和可靠性等方面存在效果差异,但它们都是研究牙本质形成复杂性不可或缺的工具。本文重点介绍动物模型和相关技术的最新进展,揭示牙本质形成中至关重要的关键分子机制。深入了解这一现象有助于谨慎选择合适的动物模型,考虑其在揭示潜在分子复杂性方面的适用性。这些见解对于开发针对牙本质相关疾病的临床药物以及制定贯穿疾病全程的综合治疗策略至关重要。

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In vivo dynamics of hard tissue-forming cell origins: Insights from Cre/loxP-based cell lineage tracing studies.硬组织形成细胞起源的体内动力学:基于Cre/loxP的细胞谱系追踪研究的见解
Jpn Dent Sci Rev. 2024 Dec;60:109-119. doi: 10.1016/j.jdsr.2024.01.003. Epub 2024 Feb 20.
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Nobody Is Perfect: Cre Drivers Deserve Careful Consideration.人无完人:Cre驱动子需要谨慎考虑。
Arterioscler Thromb Vasc Biol. 2023 Oct;43(10):2071-2074. doi: 10.1161/ATVBAHA.123.319683. Epub 2023 Aug 31.
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Biopolymers and Their Application in Bioprinting Processes for Dental Tissue Engineering.
生物聚合物及其在牙科组织工程生物打印过程中的应用。
Pharmaceutics. 2023 Aug 10;15(8):2118. doi: 10.3390/pharmaceutics15082118.
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The accuracy of quantifying the degree of hard tissue calcification using an electron probe micro analyzer, micro-focus X-ray computed tomography, and tissue sectioning methods.应用电子探针微分析仪、微焦点 X 射线计算机断层扫描和组织切片方法定量硬组织钙化程度的准确性。
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An improved method for preparing stained ground teeth sections.一种改良的染色地面牙齿切片制备方法。
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Loss of Stat3 in Osterix cells impairs dental hard tissues development.骨钙素细胞中Stat3的缺失会损害牙齿硬组织的发育。
Cell Biosci. 2023 Apr 23;13(1):75. doi: 10.1186/s13578-023-01027-1.
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In vitro, ex vivo, and in vivo models for dental pulp regeneration.牙髓再生的体外、离体和体内模型。
J Mater Sci Mater Med. 2023 Apr 1;34(4):15. doi: 10.1007/s10856-023-06718-2.
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Osteocyte Egln1/Phd2 links oxygen sensing and biomineralization via FGF23.骨细胞Egln1/Phd2通过成纤维细胞生长因子23(FGF23)连接氧感应与生物矿化。
Bone Res. 2023 Jan 18;11(1):7. doi: 10.1038/s41413-022-00241-w.
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J Biomech. 2023 Jan;147:111434. doi: 10.1016/j.jbiomech.2023.111434. Epub 2023 Jan 7.
10
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Cell Rep. 2022 Dec 6;41(10):111737. doi: 10.1016/j.celrep.2022.111737.