Department of Pediatric Dentistry, School of Dentistry, Iwate Medical University, Morioka 020-8505, Japan.
Int J Mol Med. 2012 Apr;29(4):569-73. doi: 10.3892/ijmm.2011.869. Epub 2011 Dec 23.
Although cells derived from periodontal ligament (PDL) tissue are reported to have stem cell-like activity and are speculated to play a crucial role for tissue healing and regeneration after injury or orthodontic treatment, mechanisms regulating their recruitment and activation remain unknown. Recently, stromal cell-derived factor 1α (SDF-1α) has been reported to be important for stem cell homing and recruitment to injured sites. The aim of this study was to evaluate whether fibroblast growth factor 2 (FGF-2) affects the expression of SDF-1α in PDL cells derived from human permanent teeth in vitro. Using real-time PCR, the expression of SDF-1α mRNA in PDL cells was inhibited by treatment with 10 ng/ml FGF-2. When PDL cells were treated with SU5402 (an inhibitor of FGF receptor 1) in combination with FGF-2, the FGF-2-reduced expression of SDF-1α was inhibited. In the presence of the JNK inhibitor SP600125, SDF-1α mRNA in PDL cells was not suppressed by the FGF-2 treatment. Western blot analysis also showed that SDF-1α production was suppressed by treatment with FGF-2, but it recovered with treatment by FGF-2 + SU5402. These findings suggest that SDF-1α from PDL cells plays an important role in the regeneration and homeostasis of periodontal tissues via the recruitment of stem cells.
尽管牙周膜(PDL)组织来源的细胞被报道具有干细胞样活性,并被推测在损伤或正畸治疗后对组织愈合和再生起关键作用,但调节其募集和激活的机制尚不清楚。最近,基质细胞衍生因子 1α(SDF-1α)已被报道对于干细胞归巢和募集到损伤部位非常重要。本研究旨在评估成纤维细胞生长因子 2(FGF-2)是否会影响体外来源于人恒牙的 PDL 细胞中 SDF-1α的表达。通过实时 PCR 检测,用 10ng/ml FGF-2 处理可抑制 PDL 细胞中 SDF-1α mRNA 的表达。当 PDL 细胞用 FGF 受体 1 抑制剂 SU5402 与 FGF-2 联合处理时,FGF-2 减少 SDF-1α 的表达被抑制。在 JNK 抑制剂 SP600125 的存在下,FGF-2 处理不会抑制 PDL 细胞中的 SDF-1α mRNA。Western blot 分析还表明,FGF-2 处理抑制 SDF-1α 的产生,但用 FGF-2+SU5402 处理可恢复其产生。这些发现表明,PDL 细胞来源的 SDF-1α 通过募集干细胞在牙周组织的再生和稳态中发挥重要作用。