Huang Xiaoyao, Sui Bingdong, Liu Anqi, Guo Hao, Zheng Chenxi, Liu Peisheng, Cai Xinyue, Fu Fei, Bai Shengfeng, Jin Fang, Chen Ji, Wei Changze, Jin Yan, Xuan Kun
State Key Laboratory of Oral & Maxillofacial Reconstruction and Regeneration, National Clinical Research Center for Oral Diseases, Shaanxi International Joint Research Center for Oral Disease, Center for Tissue Engineering, School of Stomatology, The Fourth Military Medical University, Xi'an, Shaanxi, 710032, China.
State Key Laboratory of Oral & Maxillofacial Reconstruction and Regeneration, National Clinical Research Center for Oral Diseases, Shaanxi Clinical Research Center for Oral Disease, Department of Preventive Dentistry, School of Stomatology, The Fourth Military Medical University, Xi'an, Shaanxi, 710032, China.
Small. 2024 Oct;20(42):e2400260. doi: 10.1002/smll.202400260. Epub 2024 Jun 11.
Harnessing the developmental events of mesenchymal condensation to direct postnatal dental stem cell aggregation represents a cutting-edge and promising approach to tooth regeneration. Tooth avulsion is among the most prevalent and serious dental injuries, and odontogenic aggregates assembled by stem cells from human exfoliated deciduous teeth (SHED) have proven effective in revitalizing avulsed teeth after replantation in the clinical trial. However, whether and how SHED aggregates (SA) communicate with recipient components and promote synergistic tissue regeneration to support replanted teeth remains elusive. Here, it is shown that SA-mediated avulsed tooth regeneration involves periodontal restoration and recovery of recipient Gli1 stem cells, which are mobilized and necessarily contribute to the reestablishment of the tooth-periodontal ligament-bone interface. Mechanistically, the release of extracellular vesicles (EVs) is revealed indispensable for the implanted SA to mobilize recipient Gli1 cells and regenerate avulsed teeth. Furthermore, SHED aggregates-released EVs (SA-EVs) are featured with odontogenic properties linked to tissue regeneration, which enhance migration, proliferation, and differentiation of Gli1 cells. Importantly, local application of SA-EVs per se empowers recipient Gli1 cells and safeguards regeneration of avulsed teeth. Collectively, the findings establish a paradigm in which odontogenesis-featured EVs govern donor-recipient stem cell interplay to achieve tooth regeneration, inspiring cell-free translational regenerative strategies.
利用间充质凝聚的发育事件来引导出生后牙齿干细胞聚集,是一种前沿且有前景的牙齿再生方法。牙齿脱臼是最常见且严重的牙齿损伤之一,在临床试验中,由人脱落乳牙干细胞(SHED)组装而成的牙源性聚集体已被证明在牙齿再植后使脱臼牙齿恢复活力方面有效。然而,SHED聚集体(SA)是否以及如何与受体成分相互作用并促进协同组织再生以支持再植牙齿,仍不清楚。在此研究中表明,SA介导的脱臼牙齿再生涉及牙周修复和受体Gli1干细胞的恢复,这些干细胞被动员起来并必然有助于牙齿 - 牙周韧带 - 骨界面的重建。从机制上讲,细胞外囊泡(EVs)的释放对于植入的SA动员受体Gli1细胞和再生脱臼牙齿是不可或缺的。此外,SHED聚集体释放的EVs(SA - EVs)具有与组织再生相关的牙源性特性,可增强Gli1细胞的迁移、增殖和分化。重要的是,局部应用SA - EVs本身就能增强受体Gli1细胞的功能并保障脱臼牙齿的再生。总体而言,这些发现建立了一种模式,即具有牙源性特征的EVs控制供体 - 受体干细胞相互作用以实现牙齿再生,为无细胞的转化性再生策略提供了启示。