Yang Xue, Han Chuyi, Yu Changhao, Zhou Bin, Ye Ling, Li Feifei, Yu Fanyuan
State Key Laboratory of Oral Diseases & National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Department of Endodontics, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Elife. 2024 Dec 20;13:RP100173. doi: 10.7554/eLife.100173.
Platelet-derived growth factor receptor alpha (PDGFR-α) activity is crucial in the process of dental and periodontal mesenchyme regeneration facilitated by autologous platelet concentrates (APCs), such as platelet-rich fibrin (PRF), platelet-rich plasma (PRP) and concentrated growth factors (CGF), as well as by recombinant PDGF drugs. However, it is largely unclear about the physiological patterns and cellular fate determinations of PDGFR-α cells in the homeostasis maintaining of adult dental and periodontal mesenchyme. We previously identified NFATc1 expressing PDGFR-α cells as a subtype of skeletal stem cells (SSCs) in limb bone in mice, but their roles in dental and periodontal remain unexplored. To this end, in the present study we investigated the spatiotemporal atlas of NFATc1 and PDGFR-α cells residing in dental and periodontal mesenchyme in mice, their capacity for progeny cell generation, and their inclusive, exclusive and hierarchical relations in homeostasis. We utilized CRISPR/Cas9-mediated gene editing to generate two dual recombination systems, which were Cre and Dre combined intersectional and exclusive reporters respectively, to concurrently demonstrate the inclusive, exclusive, and hierarchical distributions of NFATc1 and PDGFR-α cells and their lineage commitment. By employing the state-of-the-art transgenic lineage tracing techniques in cooperating with tissue clearing-based advanced imaging and three-dimensional slices reconstruction, we systematically mapped the distribution atlas of NFATc1 and PDGFR-α cells in dental and periodontal mesenchyme and tracked their in vivo fate trajectories in mice. Our findings extend current understanding of NFATc1 and PDGFR-α cells in dental and periodontal mesenchyme homeostasis, and furthermore enhance our comprehension of their sustained therapeutic impact for future clinical investigations.
血小板衍生生长因子受体α(PDGFR-α)活性在由自体血小板浓缩物(APC)促进的牙齿和牙周间充质再生过程中至关重要,例如富血小板纤维蛋白(PRF)、富血小板血浆(PRP)和浓缩生长因子(CGF),以及重组PDGF药物。然而,在成年牙齿和牙周间充质的体内平衡维持中,PDGFR-α细胞的生理模式和细胞命运决定在很大程度上尚不清楚。我们之前在小鼠四肢骨骼中鉴定出表达NFATc1的PDGFR-α细胞是骨骼干细胞(SSC)的一种亚型,但它们在牙齿和牙周中的作用仍未被探索。为此,在本研究中,我们研究了小鼠牙齿和牙周间充质中NFATc1和PDGFR-α细胞的时空图谱、它们产生子代细胞的能力,以及它们在体内平衡中的包含、排斥和层级关系。我们利用CRISPR/Cas9介导的基因编辑生成了两个双重组系统,分别是Cre和Dre组合的交叉和排斥报告基因,以同时展示NFATc1和PDGFR-α细胞的包含、排斥和层级分布及其谱系定向。通过采用最先进的转基因谱系追踪技术,并结合基于组织透明化的先进成像和三维切片重建,我们系统地绘制了NFATc1和PDGFR-α细胞在牙齿和牙周间充质中的分布图,并追踪了它们在小鼠体内的命运轨迹。我们的研究结果扩展了目前对NFATc1和PDGFR-α细胞在牙齿和牙周间充质体内平衡中的理解,并且进一步增强了我们对它们在未来临床研究中持续治疗影响的理解。