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体外模拟人类牙齿发育的早期阶段。

Emulating the early phases of human tooth development in vitro.

机构信息

Technische Universität Berlin, Institute of Biotechnology, Department Medical Biotechnology, Gustav-Meyer-Allee 25, 13355, Berlin, Germany.

Institute of Experimental Pediatric Endocrinology, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany.

出版信息

Sci Rep. 2019 May 7;9(1):7057. doi: 10.1038/s41598-019-43468-0.

Abstract

Functional in vitro models emulating the physiological processes of human organ formation are invaluable for future research and the development of regenerative therapies. Here, a developmentally inspired approach is pursued to reproduce fundamental steps of human tooth organogenesis in vitro using human dental pulp cells. Similar to the in vivo situation of tooth initiating mesenchymal condensation, a 3D self-organizing culture was pursued resulting in an organoid of the size of a human tooth germ with odontogenic marker expression. Furthermore, the model is capable of epithelial invagination into the condensed mesenchyme, mimicking the reciprocal tissue interactions of human tooth development. Comprehensive transcriptome analysis revealed activation of well-studied as well as rather less investigated signaling pathways implicated in human tooth organogenesis, such as the Notch signaling. Early condensation in vitro revealed a shift to the TGFß signal transduction pathway and a decreased RhoA small GTPase activity, connected to the remodeling of the cytoskeleton and actin-mediated mechanotransduction. Therefore, this in vitro model of tooth development provides a valuable model to study basic human developmental mechanisms.

摘要

体外功能性模型模拟人类器官形成的生理过程,对于未来的研究和再生疗法的发展非常宝贵。在这里,我们采用一种受发育启发的方法,使用人牙髓细胞在体外再现人类牙齿器官发生的基本步骤。类似于牙齿起始间充质凝聚的体内情况,我们进行了 3D 自组织培养,导致形成具有成牙本质标志物表达的人类牙胚大小的类器官。此外,该模型能够使上皮细胞向内陷入凝聚的间充质,模拟人类牙齿发育中相互作用的组织。全面的转录组分析揭示了激活了在人类牙齿发生中具有良好研究基础的信号通路以及研究较少的信号通路,如 Notch 信号通路。体外早期凝聚显示 TGFβ信号转导途径的转变和 RhoA 小 GTPase 活性的降低,与细胞骨架的重塑和肌动蛋白介导的机械转导有关。因此,这种牙齿发育的体外模型为研究基本的人类发育机制提供了一个有价值的模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/957c/6505527/2924e4210aa7/41598_2019_43468_Fig1_HTML.jpg

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