Osteogenic differentiation of periodontal ligament fibroblasts inhibits osteoclast formation

IF 4.5 3区 生物学 Q2 CELL BIOLOGY
Caya M. Prins , Merve Ceylan , Jolanda M.A. Hogervorst , Ineke D.C. Jansen , Irene M. Schimmel , Ton Schoenmaker , Teun J. de Vries
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引用次数: 0

Abstract

One of the deficits of knowledge on bone remodelling, is to what extent cells that are driven towards osteogenic differentiation can contribute to osteoclast formation. The periodontal ligament fibroblast (PdLFs) is an ideal model to study this, since they play a role in osteogenesis, and can also orchestrate osteoclastogenesis.when co-cultured with a source of osteoclast-precursor such as peripheral blood mononuclear cells (PBMCs). Here, the osteogenic differentiation of PdLFs and the effects of this process on the formation of osteoclasts were investigated. PdLFs were obtained from extracted teeth and exposed to osteogenic medium for 0, 7, 14, or 21 out of 21 days. After this 21-day culturing period, the cells were co-cultured with peripheral blood mononuclear cells (PBMCs) for an additional 21 days to study osteoclast formation. Alkaline phosphatase (ALP) activity, calcium concentration, and gene expression of osteogenic markers were assessed at day 21 to evaluate the different stages of osteogenic differentiation. Alizarin red staining and scanning electron microscopy were used to visualise mineralisation. Tartrate-resistant acid phosphatase (TRAcP) activity, TRAcP staining, multinuclearity, the expression of osteoclastogenesis-related genes, and TNF-α and IL-1β protein levels were assessed to evaluate osteoclastogenesis. The osteogenesis assays revealed that PdLFs became more differentiated as they were exposed to osteogenic medium for a longer period of time. Mineralisation by these osteogenic cells increased with the progression of differentiation. Culturing PdLFs in osteogenic medium before co-culturing them with PMBCs led to a significant decrease in osteoclast formation. qPCR revealed significantly lower DCSTAMP expression in cultures that had been supplemented with osteogenic medium. Protein levels of osteoclastogenesis stimulator TNF-α were also lower in these cultures. The present study shows that the osteogenic differentiation of PdLFs reduces the osteoclastogenic potential of these cells. Immature cells of the osteoblastic lineage may facilitate osteoclastogenesis, whereas mature mineralising cells may suppress the formation of osteoclasts. Therefore, mature and immature osteogenic cells may have different roles in maintaining bone homeostasis.

牙周韧带成纤维细胞的成骨分化可抑制破骨细胞的形成
骨重塑知识的一个缺陷是,成骨分化细胞在多大程度上能促进破骨细胞的形成。牙周韧带成纤维细胞(PdLFs)是研究这一问题的理想模型,因为它们不仅在成骨过程中发挥作用,而且在与破骨细胞前体源(如外周血单核细胞(PBMCs))共同培养时也能协调破骨细胞的形成。本文研究了 PdLFs 的成骨分化及其对破骨细胞形成的影响。PdLFs 取自拔出的牙齿,在成骨培养基中暴露 0、7、14 或 21 天。在这 21 天的培养期结束后,再与外周血单核细胞(PBMC)共同培养 21 天,以研究破骨细胞的形成。在第 21 天评估碱性磷酸酶(ALP)活性、钙浓度和成骨标志物的基因表达,以评价成骨分化的不同阶段。茜素红染色和扫描电子显微镜用于观察矿化过程。抗酒石酸磷酸酶(TRAcP)活性、TRAcP染色、多核性、破骨细胞生成相关基因的表达以及TNF-α和IL-1β蛋白水平被用来评估破骨细胞生成。成骨试验显示,PdLFs在成骨培养基中暴露时间越长,分化程度越高。这些成骨细胞的矿化程度随着分化的进展而增加。在将 PdLFs 与 PMBCs 共同培养之前先用成骨培养基培养它们,可显著减少破骨细胞的形成。在这些培养物中,破骨细胞生成刺激因子 TNF-α 的蛋白水平也较低。本研究表明,PdLFs 的成骨分化降低了这些细胞的破骨细胞生成潜能。成骨细胞系的未成熟细胞可能会促进破骨细胞的生成,而成熟的矿化细胞可能会抑制破骨细胞的形成。因此,成熟和不成熟的成骨细胞在维持骨平衡方面可能有不同的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
European journal of cell biology
European journal of cell biology 生物-细胞生物学
CiteScore
7.30
自引率
1.50%
发文量
80
审稿时长
38 days
期刊介绍: The European Journal of Cell Biology, a journal of experimental cell investigation, publishes reviews, original articles and short communications on the structure, function and macromolecular organization of cells and cell components. Contributions focusing on cellular dynamics, motility and differentiation, particularly if related to cellular biochemistry, molecular biology, immunology, neurobiology, and developmental biology are encouraged. Manuscripts describing significant technical advances are also welcome. In addition, papers dealing with biomedical issues of general interest to cell biologists will be published. Contributions addressing cell biological problems in prokaryotes and plants are also welcome.
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