State Key Laboratory of Oral Diseases, National Clinical Research Centre for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, Sichuan, China; Department of Conservative Dentistry and Endodontics, West China Hospital of Stomatology, Sichuan University, Chengdu, Sichuan, China.
State Key Laboratory of Oral Diseases, National Clinical Research Centre for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, Sichuan, China; Department of Oral and Maxillofacial Surgery, West China Hospital of Stomatology, Sichuan University, Chengdu, Sichuan, China.
J Endod. 2022 Aug;48(8):1029-1037. doi: 10.1016/j.joen.2022.05.001. Epub 2022 May 8.
During cell-free regenerative endodontic therapy, both stem cells from apical papilla (SCAPs) and periodontal ligament cells (PDLCs) are possible cell sources because of their proximity. Nonetheless, the regenerative ability of PDLCs and SCAPs under the induction of concentrated growth factors (CGFs) remains unclear.
PDLCs and SCAPs were treated with various concentrations of CGF-conditioned medium (CCM). The effects of CCM with or without Porphyromonas gingivalis lipopolysaccharide (LPS) on cell migration, odonto/osteogenic differentiation, and the expression of inflammatory cytokines were assessed. Dentin matrix transplants composed of PDLCs or SCAPs cell sheets coupled with CGF were put subcutaneously in immunocompromised mice for 8 weeks to explore their regenerative characteristics in vivo.
CCM dose dependently enhanced the migration, proliferation, and odonto/osteogenic differentiation of PDLCs and SCAPs. CCM alleviated LPS-inhibited odonto/osteogenic differentiation of PDLCs and SCAPs as well as the LPS-induced up-regulation of inflammatory cytokines. In vivo, the newly regenerated tissue and microvessels formed by PDLCs and SCAPs were significantly increased under the induction of CGF. SCAPs mainly regenerated pulp/dentinlike tissues and a large number of microvessels, whereas PDLCs mainly formed bone/cementumlike structures.
Overall, PDLCs excelled in cell proliferation, migration, and osteogenic differentiation, whereas SCAPs outperformed PDLCs in terms of angiogenic and odontogenic differentiation. The biological differences between PDLCs and SCAPs provided a possible theoretical basis for the formation of bone/cementum/periodontal ligament-like tissues after cell-free regenerative endodontic therapy.
在无细胞再生性牙髓治疗中,由于根尖乳头干细胞(SCAPs)和牙周膜细胞(PDLCs)位置接近,因此两者都可能成为细胞来源。然而,在浓缩生长因子(CGFs)的诱导下,PDLCs 和 SCAPs 的再生能力尚不清楚。
用不同浓度的 CGF 条件培养基(CCM)处理 PDLCs 和 SCAPs。评估 CCM 对细胞迁移、牙/骨向分化以及炎症细胞因子表达的影响,以及 CCM 联合或不联合牙龈卟啉单胞菌脂多糖(LPS)对细胞迁移、牙/骨向分化以及炎症细胞因子表达的影响。将 PDLCs 或 SCAPs 细胞片与 CGF 结合的牙本质基质移植物皮下植入免疫功能低下的小鼠体内 8 周,以研究其体内再生特性。
CCM 呈剂量依赖性增强 PDLCs 和 SCAPs 的迁移、增殖和牙/骨向分化。CCM 缓解了 LPS 抑制的 PDLCs 和 SCAPs 的牙/骨向分化以及 LPS 诱导的炎症细胞因子的上调。在体内,PDLCs 和 SCAPs 在 CGF 的诱导下,新生组织和微血管的形成明显增加。SCAPs 主要再生牙髓/牙本质样组织和大量微血管,而 PDLCs 主要形成骨/牙骨质样结构。
总的来说,PDLCs 在细胞增殖、迁移和成骨分化方面表现出色,而 SCAPs 在血管生成和牙向分化方面优于 PDLCs。PDLCs 和 SCAPs 之间的生物学差异为无细胞再生性牙髓治疗后形成骨/牙骨质/牙周膜样组织提供了可能的理论基础。