State Key Laboratory of Oral Disease, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
National Engineering Laboratory for Oral Regenerative Medicine, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
J Cell Physiol. 2020 Mar;235(3):2698-2709. doi: 10.1002/jcp.29174. Epub 2019 Sep 12.
Hertwig's epithelial root sheath (HERS) is critical for epithelial-mesenchymal interaction (EMI) during tooth root formation. However, the exact roles of HERS in odontogenic differentiation by EMI have not been well characterized, because primary HERS cells are difficult to obtain. Immortalized cell lines constitute crucial scientific tools, while there are few HERS cell lines available. Our previous study has successfully established immortalized HERS cell lines. Here, we confirmed the phenotype of our HERS-H1 by verifying its characteristics and functions in odontogenic differentiation through EMI. The HERS-H1-conditioned medium (CM-H1) effectively enhanced odontogenic differentiation of dental papilla cells (DPCs) in vitro. Furthermore, Smad4 and p-Smad1/5/8 were significantly activated in DPCs treated with CM-H1, and this activation was attenuated by noggin. In vivo, our implanted recombinants of HERS-H1 and DPCs exhibited mineralized tissue formation and expression of Smad4, p-Smad1/5/8, and odontogenic differentiation markers. Our results indicated that HERS-H1 promoted DPCs odontoblastic differentiation via bone morphogenetic protein/Smad signaling. HERS-H1 exhibits relevant key molecular characteristics and constitutes a new biological model for basic research on HERS and the dental EMI during root development and regeneration.
赫特维希上皮根鞘(HERS)在牙齿根部形成过程中的上皮-间充质相互作用(EMI)中至关重要。然而,HERS 在 EMI 诱导的牙源性分化中的确切作用尚未得到很好的描述,因为原代 HERS 细胞难以获得。永生化细胞系构成了重要的科学工具,而 HERS 细胞系却很少。我们之前的研究已经成功建立了永生化的 HERS 细胞系。在这里,我们通过 EMI 验证了 HERS-H1 在牙源性分化中的特性和功能,从而证实了 HERS-H1 的表型。HERS-H1 条件培养基(CM-H1)可有效增强体外牙乳头细胞(DPC)的牙源性分化。此外,CM-H1 处理的 DPC 中 Smad4 和 p-Smad1/5/8 明显被激活,而 noggin 则减弱了这种激活。在体内,我们植入的 HERS-H1 和 DPC 的重组体表现出矿化组织形成和 Smad4、p-Smad1/5/8 以及牙源性分化标志物的表达。我们的结果表明,HERS-H1 通过骨形态发生蛋白/Smad 信号促进 DPC 成牙本质细胞分化。HERS-H1 表现出相关的关键分子特征,并构成了 HERS 及其在根发育和再生过程中牙齿 EMI 的基础研究的新生物学模型。
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