甲状旁腺激素相关蛋白在人牙囊细胞成骨分化过程中分泌,并抑制碱性磷酸酶活性和DLX3的表达。
The parathyroid hormone-related protein is secreted during the osteogenic differentiation of human dental follicle cells and inhibits the alkaline phosphatase activity and the expression of DLX3.
作者信息
Klingelhöffer C, Reck A, Ettl T, Morsczeck C
机构信息
Department of Cranio- and Maxillofacial Surgery, Hospital of the University of Regensburg, Regensburg, Germany.
Department of Cranio- and Maxillofacial Surgery, Hospital of the University of Regensburg, Regensburg, Germany.
出版信息
Tissue Cell. 2016 Aug;48(4):334-9. doi: 10.1016/j.tice.2016.05.007. Epub 2016 Jun 1.
The dental follicle is involved in tooth eruption and it expresses a great amount of the parathyroid hormone-related protein (PTHrP). PTHrP as an extracellular protein is required for a multitude of different regulations of enchondral bone development and differentiation of bone precursor cells and of the development of craniofacial tissues. The dental follicle contains also precursor cells (DFCs) of the periodontium. Isolated DFCs differentiate into periodontal ligament cells, alveolar osteoblast and cementoblasts. However, the role of PTHrP during the human periodontal development remains elusive. Our study evaluated the influence of PTHrP on the osteogenic differentiation of DFCs under in vitro conditions for the first time. The PTHrP protein was highly secreted after 4days of the induction of the osteogenic differentiation of DFCs with dexamethasone (2160.5pg/ml±345.7SD. in osteogenic differentiation medium vs. 315.7pg/ml±156.2SD. in standard cell culture medium; Student's t Test: p<0.05 (n=3)). We showed that the supplementation of the osteogenic differentiation medium with PTHrP inhibited the alkaline phosphatase activity and the expression of the transcription factor DLX3, but the depletion of PTHrP did not support the differentiation of DFCs. Previous studies have shown that Indian Hedgehog (IHH) induces PTHrP and that PTHrP, in turn, inhibits IHH via a negative feedback loop. We showed that SUFU (Suppressor Of Fused Homolog) was not regulated during the osteogenic differentiation in DFCs. So, neither the hedgehog signaling pathway induced PTHrP nor PTHrP suppressed the hedgehog signaling pathway during the osteogenic differentiation in DFCs. In conclusion, our results suggest that PTHrP regulates independently of the hedgehog signaling pathway the osteogenic differentiated in DFCs.
牙囊参与牙齿萌出,且表达大量甲状旁腺激素相关蛋白(PTHrP)。PTHrP作为一种细胞外蛋白,对于软骨内骨发育、骨前体细胞分化以及颅面组织发育的多种不同调节是必需的。牙囊还含有牙周组织的前体细胞(DFCs)。分离出的DFCs可分化为牙周膜细胞、牙槽成骨细胞和成牙骨质细胞。然而,PTHrP在人类牙周发育过程中的作用仍不清楚。我们的研究首次评估了PTHrP在体外条件下对DFCs成骨分化的影响。在用地塞米松诱导DFCs成骨分化4天后,PTHrP蛋白分泌量很高(在成骨分化培养基中为2160.5pg/ml±345.7SD,而在标准细胞培养基中为315.7pg/ml±156.2SD;学生t检验:p<0.05(n = 3))。我们发现,在成骨分化培养基中添加PTHrP会抑制碱性磷酸酶活性和转录因子DLX3的表达,但去除PTHrP并不促进DFCs的分化。先前的研究表明,印度刺猬因子(IHH)诱导PTHrP,而PTHrP反过来通过负反馈环抑制IHH。我们发现,在DFCs成骨分化过程中,SUFU(融合抑制同源物)不受调控。因此,在DFCs成骨分化过程中,刺猬信号通路既不诱导PTHrP,PTHrP也不抑制刺猬信号通路。总之,我们的结果表明,PTHrP独立于刺猬信号通路调节DFCs的成骨分化。