State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Disease, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Department of Oral Implantology, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
J Cell Mol Med. 2020 Oct;24(19):11457-11464. doi: 10.1111/jcmm.15754. Epub 2020 Aug 26.
Dental stem cell-based tooth regeneration is the futuristic treatment for missing teeth. Growth differentiation factor 11 (GDF11), a novel member of the TGF-beta superfamily, has been reported to play a critical role in regulating stem cell differentiation. However, the role of endogenous GDF11 during dental stem cell differentiation remains unknown. Here, we have shown that GDF11 was highly expressed in dental pulp tissues in both mouse and human. Knockdown of endogenous GDF11 in human dental pulp stem cells (hDPSCs) led to comparable proliferation and migration but attenuated odontogenic differentiation as evidenced by alkaline phosphatase and Alizarin Red S staining. In addition, transcriptional levels of odontogenic-related genes were significantly down-regulated according to real-time polymerase chain reaction. Mechanistically, we performed RNA sequencing analysis and found that silencing of endogenous GDF11 compromised the process of ossification and osteoblast differentiation, especially down-regulated transcription expression of Wnt pathway-specific genes. Immunofluorescence staining also showed diminished β-catenin expression and nuclei accumulation after knockdown of endogenous GDF11 in hDPSCs. In summary, our results suggested that endogenous GDF11 positively regulate odontogenic differentiation of hDPSCs through canonical Wnt/β-catenin signalling pathway.
基于牙干细胞的牙齿再生是治疗缺失牙齿的未来疗法。生长分化因子 11(GDF11)是 TGF-β超家族的一个新成员,据报道它在调节干细胞分化中起着关键作用。然而,内源性 GDF11 在牙干细胞分化过程中的作用尚不清楚。在这里,我们已经表明 GDF11 在人和小鼠的牙髓组织中高度表达。在人牙髓干细胞(hDPSCs)中敲低内源性 GDF11 导致相似的增殖和迁移,但牙向分化减弱,碱性磷酸酶和茜素红 S 染色证实了这一点。此外,根据实时聚合酶链反应,牙向相关基因的转录水平显著下调。从机制上讲,我们进行了 RNA 测序分析,发现内源性 GDF11 的沉默会损害成骨和成骨细胞分化的过程,特别是下调 Wnt 通路特异性基因的转录表达。免疫荧光染色也显示在 hDPSCs 中敲低内源性 GDF11 后 β-连环蛋白表达和核积累减少。总之,我们的结果表明内源性 GDF11 通过经典的 Wnt/β-连环蛋白信号通路正向调节 hDPSCs 的牙向分化。
J Cell Mol Med. 2020-10
BMC Oral Health. 2023-4-6
Hua Xi Kou Qiang Yi Xue Za Zhi. 2022-1-25
Int J Mol Sci. 2023-4-22
J Dent Res. 2019-3-20
J Dent Res. 2017-12-1
J Dent Res. 2017-11-29
J Dent Res. 2018-1