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牙源性再生中牙囊干细胞的表观遗传调控

Epigenetic Regulation of Dental Follicle Stem Cells in Odontogenic Regeneration.

作者信息

Gultekin Sibel Elif, Arslan Bozdag Leyla, Odenthal Margarete, Dienes Hans-Peter

机构信息

Department of Oral Pathology, Dental Faculty, Gazi University, Ankara, Turkey.

Department of Biology, Faculty of Science, Gazi University, Ankara, Turkey.

出版信息

J Cell Mol Med. 2025 May;29(9):e70541. doi: 10.1111/jcmm.70541.

Abstract

MicroRNAs (miRNAs) are short non-coding RNAs essential for biological functions that control the process of translation of mRNA into protein. The discovery of miRNAs in mesenchymal stem cells (MSCs), especially in odontogenic tissues and dental follicles, has not been fully characterised. This study focused on characterising dental follicle stem cells (DFSCs) in terms of their ability to proliferate and differentiate into osteoblasts using qRT-PCR (miR-203, miR-125 and miR-21) and immunohistochemistry (OCT4 and CD133). Dental follicles are essential for tooth eruption as they envelop the enamel organ and dental papilla and control the development and breakdown of the alveolar bone. Dental follicle progenitor cells (DFPCs) are stem cells located in dental follicles that differentiate into several cell types that are essential for tooth development and eruption. We observed that miR-125 was upregulated in fibromyxoid and myxoid tissues during odonto/osteogenic differentiation of hDFPCs (fold change values, respectively, 1.75 ± 0.98 and 2.17 ± 1.03). miR-203 and miR-21 significantly downregulated odonto/osteogenic differentiation in myxoid, fibromyxoid and fibroid tissues (fold change values, respectively: miR-203: 0.57 ± 0.25, 0.38 ± 0.11, 0.21 ± 0.18; miR-21: 0.21 ± 0.14, 0.21 ± 0.13, 0.082 ± 0.14). Ultimately, utilising miRNA signatures in humans as a predictive tool will help us understand the molecular processes involved in DFSCs.

摘要

微小RNA(miRNA)是短链非编码RNA,对控制mRNA转化为蛋白质的翻译过程的生物学功能至关重要。间充质干细胞(MSC)中,尤其是在牙源性组织和牙囊中,miRNA的发现尚未得到充分表征。本研究聚焦于使用qRT-PCR(miR-203、miR-125和miR-21)和免疫组织化学(OCT4和CD133)对牙囊干细胞(DFSC)增殖和分化为成骨细胞的能力进行表征。牙囊对于牙齿萌出至关重要,因为它们包裹着牙釉质器官和牙乳头,并控制牙槽骨的发育和分解。牙囊祖细胞(DFPC)是位于牙囊中的干细胞,可分化为几种对牙齿发育和萌出至关重要的细胞类型。我们观察到,在人DFPC的成牙本质/成骨分化过程中,miR-125在纤维黏液样和黏液样组织中上调(倍数变化值分别为1.75±0.98和2.17±1.03)。miR-203和miR-21在黏液样、纤维黏液样和纤维样组织中显著下调成牙本质/成骨分化(倍数变化值分别为:miR-203:0.57±0.25、0.38±0.11、0.21±0.18;miR-21:0.21±0.14、0.21±0.13、0.082±0.14)。最终,将人类中的miRNA特征用作预测工具将有助于我们了解DFSC中涉及的分子过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4638/12037698/3a9841f2f5d7/JCMM-29-e70541-g005.jpg

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