Department of Restorative Dentistry and Periodontology, Faculty of Dentistry, Chiang Mai University, Chiang Mai 50200, Thailand.
Center of Excellence in Oral and Maxillofacial Biology, Department of Oral Biology and Diagnostic Sciences, Faculty of Dentistry, Chiang Mai University, Chiang Mai 50200, Thailand.
Arch Oral Biol. 2017 Nov;83:130-135. doi: 10.1016/j.archoralbio.2017.07.017. Epub 2017 Jul 25.
Based on our earlier work on the response of periodontal ligament (PDL) cells to mechanical stress by induction of cyclooxygenase expression and production of prostaglandin PGE that could regulate mineralization of PDL cells, it was hypothesized that PGE had potential effects on PDL stemness. In this study, we aimed to investigate clonogenicity, proliferation and expression of certain pluripotent markers, considered to be characteristics of PDL stemness, in response to treatment with exogenously-added PGE.
Human PDL cells were cultured and treated with various doses of PGE, and the aforementioned characteristics of PDL stemness were analyzed.
The clonogenicity and proliferation were significantly enhanced by PGE at low concentrations (0.01, 0.1 and 1ng/ml; P<0.05), but only the proliferation was significantly diminished by PGE at a high concentration (100ng/ml; P<0.05). Expression of NANOG and OCT4 mRNA and protein was increased by PGE treatment at 0.1 and 1ng/ml. Consistently, expression of stage-specific embryonic antigen 4, a putative stem cell marker, was significantly augmented by PGE treatment at 1ng/ml (P<0.05).
Our findings suggest that although a high dose of PGE (100ng/ml) inhibits proliferation of PDL cells, PGE at low doses appears to play a role in the maintenance of PDL stemness.
基于我们之前关于牙周膜(PDL)细胞对机械应激的反应的研究,通过诱导环氧化酶表达和产生前列腺素 PGE,可调节 PDL 细胞的矿化,我们假设 PGE 对 PDL 干细胞具有潜在影响。在这项研究中,我们旨在研究外源性添加 PGE 对 PDL 干细胞特性的克隆形成、增殖和某些多能标志物表达的影响。
培养人牙周膜细胞并用不同剂量的 PGE 处理,分析 PDL 干细胞特性。
低浓度(0.01、0.1 和 1ng/ml;P<0.05)的 PGE 显著增强了克隆形成和增殖,但高浓度(100ng/ml;P<0.05)的 PGE 仅显著降低了增殖。0.1 和 1ng/ml 的 PGE 处理增加了 NANOG 和 OCT4 mRNA 和蛋白的表达。同样,1ng/ml 的 PGE 处理显著增加了阶段特异性胚胎抗原 4 的表达,这是一种假定的干细胞标志物(P<0.05)。
我们的发现表明,尽管高剂量的 PGE(100ng/ml)抑制了 PDL 细胞的增殖,但低剂量的 PGE 似乎在维持 PDL 干细胞特性方面发挥作用。