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在基因靶向小鼠模型中研究釉质形成的挑战。

Challenges of Studying Amelogenesis in Gene-Targeted Mouse Models.

作者信息

Smith Charles E, Bartlett John D, Simmer James P, Hu Jan C-C

机构信息

Department of Anatomy & Cell Biology, Faculty of Medicine & Health Sciences, McGill University, 3640 University St., Montreal, QC H3A 0C7, Canada.

Department of Biologic and Materials Sciences, University of Michigan School of Dentistry, 1011 North University Ave., Ann Arbor, MI 48190, USA.

出版信息

Int J Mol Sci. 2025 May 20;26(10):4905. doi: 10.3390/ijms26104905.

Abstract

Research on how a stratified oral epithelium gained the capability to create the hardest hydroxyapatite-based mineralized tissue produced biologically to protect the surfaces of teeth has been ongoing for at least 175 years. Many advances have been made in unraveling some of the key factors that allowed the innermost undifferentiated epithelial cells sitting on a skin-type basement membrane to transform into highly polarized cells capable of forming and controlling the mineralization of the extracellular organic matrix that becomes enamel. Genetic manipulation of mice has proven to be a useful approach for studying specific events in the amelogenesis developmental sequence but there have been pitfalls in interpreting loss of function data caused in part by conflicting literature, technical problems in tissue preservation, and the total amount of time spent on tooth development between different species that have led to equivocal conclusions. This critical review attempts to discuss some of these issues and highlight the challenges of characterizing amelogenesis in gene-targeted mouse models.

摘要

关于分层口腔上皮如何获得能力,以产生生物学上生成的最坚硬的基于羟基磷灰石的矿化组织来保护牙齿表面的研究,至少已经进行了175年。在揭示一些关键因素方面已经取得了许多进展,这些因素使得位于皮肤型基底膜上的最内层未分化上皮细胞能够转变为高度极化的细胞,这些细胞能够形成并控制形成牙釉质的细胞外有机基质的矿化。事实证明,对小鼠进行基因操作是研究釉质形成发育序列中特定事件的一种有用方法,但在解释功能丧失数据时存在一些陷阱,部分原因是文献相互矛盾、组织保存中的技术问题,以及不同物种之间牙齿发育所花费的总时间,这些都导致了模棱两可的结论。这篇批判性综述试图讨论其中的一些问题,并强调在基因靶向小鼠模型中表征釉质形成的挑战。

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