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维甲酸信号负向调节牙髓干细胞的成骨/成牙分化。

Retinoic Acid Signal Negatively Regulates Osteo/Odontogenic Differentiation of Dental Pulp Stem Cells.

作者信息

Wang Jiangyi, Li Guoqing, Hu Lei, Yan Fei, Zhao Bin, Wu Xiaoshan, Zhang Chunmei, Wang Jinsong, Du Juan, Wang Songlin

机构信息

Laboratory of Molecular Signaling and Stem Cell Therapy, Beijing Key Laboratory of Tooth Regeneration and Function Reconstruction, Capital Medical University School of Stomatology, Beijing, China.

Molecular Laboratory for Gene Therapy and Tooth Regeneration, Beijing Key Laboratory of Tooth Regeneration and Function Reconstruction, Capital Medical University School of Stomatology, Beijing, China.

出版信息

Stem Cells Int. 2020 Jun 27;2020:5891783. doi: 10.1155/2020/5891783. eCollection 2020.

Abstract

Retinoic acid (RA) signal is involved in tooth development and osteogenic differentiation of mesenchymal stem cells (MSCs). Dental pulp stem cells (DPSCs) are one of the useful MSCs in tissue regeneration. However, the function of RA in osteo/odontogenic differentiation of DPSCs remains unclear. Here, we investigated the expression pattern of RA in miniature pig tooth germ and intervened in the RA signal during osteo/odontogenic differentiation of human DPSCs. Deciduous canine (DC) germs of miniature pigs were observed morphologically, and the expression patterns of RA were studied by hybridization (ISH). Human DPSCs were isolated and cultured in osteogenic induction medium with or without RA or BMS 493, an inverse agonist of the pan-retinoic acid receptors (pan-RARs). Alkaline phosphatase (ALP) activity assays, alizarin red staining, quantitative calcium analysis, CCK8 assay, osteogenesis-related gene expression, and transplantation were conducted to determine the osteo/odontogenic differentiation potential and proliferation potential of DPSCs. We found that the expression of and decreased during crown calcification of DCs of miniature pigs. Activation of RA signal inhibited ALP activities and mineralization of human DPSCs and decreased the mRNA expression of , , , and a transcription factor, . With BMS 493 treatment, the results were opposite. Interference in RA signal decreased the proliferation of DPSCs. transplantation experiments suggested that osteo/odontogenic differentiation potential of DPSCs was enhanced by inversing RA signal. Our results demonstrated that downregulation of RA signal promoted osteo/odontogenic differentiation of DPSCs and indicated a potential target pathway to improve tissue regeneration.

摘要

维甲酸(RA)信号参与牙齿发育和间充质干细胞(MSC)的成骨分化。牙髓干细胞(DPSC)是组织再生中有用的间充质干细胞之一。然而,RA在DPSC的骨/牙源性分化中的功能仍不清楚。在此,我们研究了RA在小型猪牙胚中的表达模式,并在人DPSC的骨/牙源性分化过程中干预RA信号。对小型猪的乳牙犬齿(DC)牙胚进行形态学观察,并通过原位杂交(ISH)研究RA的表达模式。分离人DPSC,并在含有或不含有RA或全反式维甲酸受体(pan-RARs)反向激动剂BMS 493的成骨诱导培养基中培养。进行碱性磷酸酶(ALP)活性测定、茜素红染色、定量钙分析、CCK8测定、成骨相关基因表达和体内移植,以确定DPSC的骨/牙源性分化潜能和增殖潜能。我们发现,在小型猪DC的冠部钙化过程中,RA和RAR的表达降低。RA信号的激活抑制了人DPSC的ALP活性和矿化,并降低了Runx2、Osx、Col1a1和转录因子Osterix的mRNA表达。用BMS 493处理后,结果相反。对RA信号的干扰降低了DPSC的增殖。体内移植实验表明,通过逆转RA信号可增强DPSC的骨/牙源性分化潜能。我们的结果表明,RA信号的下调促进了DPSC的骨/牙源性分化,并表明了一条改善组织再生的潜在靶标途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c571/7336240/99d0a67ecfc0/SCI2020-5891783.001.jpg

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