Key Laboratory of Oral Biomedicine of Ministry of Education and Department of Endodontics, School and Hospital of Stomatology, Wuhan University, Wuhan, Hubei Province, PR China.
J Cell Biochem. 2012 Feb;113(2):669-77. doi: 10.1002/jcb.23396.
Postnatal dental pulp stem cells (DPSCs) represent a unique precursor population in the dental pulp, which have multipotential and harbor great potential for tissue engineering purposes. However, for therapy applications, transplanted cells are often exposed to unfavorable conditions such as cytokines released from necrotic or inflammatory cells in injured tissues. It is not clear how stem cells exposed to these conditions changes in their characteristics. In this study, the effects of pro-inflammatory cytokines, such as IL-1 and TNF, on DPSCs were investigated. Cells were treated with IL-1, TNF, or both for 3, 7, and 12 days. The cultures were evaluated for cell proliferation, ALP activity, and real-time PCR. We found that a short treatment (3 days) of pro-inflammatory cytokines induced the odontogenic differentiation of DPSCs. Furthermore, post 3 days treatment with pro-inflammatory cytokines, the cell-scaffold complexes were implanted subcutaneously in mice for 8 weeks. Histological analysis demonstrated that the cultures gave obviously mineralized tissue formation, especially for both IL-1 and TNF applied. These data suggest that IL-1 and TNF produced in the early inflammatory reaction may induce the mineralization of DPSCs.
牙髓干细胞(DPSCs)是牙髓中一种独特的前体细胞群,具有多能性,在组织工程中有很大的应用潜力。然而,对于治疗应用,移植细胞通常会暴露于不利条件下,例如来自损伤组织中坏死或炎症细胞释放的细胞因子。目前尚不清楚暴露于这些条件下的干细胞的特征会发生怎样的变化。在这项研究中,我们研究了促炎细胞因子(如 IL-1 和 TNF)对 DPSCs 的影响。将细胞用 IL-1、TNF 或两者共同处理 3、7 和 12 天。通过细胞增殖、碱性磷酸酶(ALP)活性和实时 PCR 评估培养物。我们发现,促炎细胞因子的短期(3 天)处理可诱导 DPSCs 的成牙本质分化。此外,在促炎细胞因子处理 3 天后,将细胞-支架复合物皮下植入小鼠体内 8 周。组织学分析表明,培养物明显形成矿化组织,特别是同时应用 IL-1 和 TNF 的情况下。这些数据表明,早期炎症反应中产生的 IL-1 和 TNF 可能诱导 DPSCs 的矿化。