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Direct cell-cell contact between periodontal ligament fibroblasts and osteoclast precursors synergistically increases the expression of genes related to osteoclastogenesis

机译:牙周膜成纤维细胞与破骨细胞前体之间的直接细胞间接触协同增加了与破骨细胞发生有关的基因的表达

摘要

The formation of bone resorbing osteoclasts in vivo is orchestrated by cells of the osteoblast lineage such as periodontal ligament fibroblasts that provide the proper signals to osteoclast precursors. Although the requirement of cell-cell interactions is widely acknowledged, it is unknown whether these interactions influence the expression of genes required for osteoclastogenesis and the ultimate formation of osteoclasts. In the present study we investigated the effect of cell-cell interaction on the mRNA expression of adhesion molecules and molecules involved in osteoclast formation in cultures of peripheral blood mononuclear cells (PBMCs) and human primary periodontal ligament fibroblasts, both as solitary cultures and in co-culture. We further analyzed the formation of multinucleated, tartrate resistant acid phosphatase (TRACP) positive cells and assessed their bone resorbing abilities. Interestingly, gene expression of intercellular adhesion molecule-1 (ICAM-1) and of osteoclastogenesis-related genes (RANKL, RANK, TNF-alpha, and IL-1 beta) was highly up-regulated in the co-cultures compared to mono-cultures and the 5-10-fold up-regulation reflected a synergistic increase due to direct cell-cell interaction. This induction strongly overpowered the effects of known osteoclastogenesis inducers I,25(OH)(2)VitD(3) and dexamethasone. In case of indirect cell-cell contact mRNA expression was not altered, indicating that heterotypic adhesion is required for the increase in gene expression. In addition, the number of osteoclast-like cells that were formed in co-culture with periodontal ligament fibroblasts was significantly augmented compared to mono-cultures. Our data indicate that cell-cell adhesion between osteoclast precursors and periodontal ligament fibroblasts significantly modulates the cellular response which favors the expression of osteoclast differentiation genes and the ultimate formation of osteoclasts. J. Cell. Physiol. 222: 565-573, 2010. (C) 2009 Wiley-Liss, Inc.
机译:体内吸收骨破骨细胞的形成是由成骨细胞谱系(例如牙周膜成纤维细胞)的细胞编排的,这些细胞向破骨细胞前体提供适当的信号。尽管细胞间相互作用的要求已得到广泛认可,但尚不清楚这些相互作用是否影响破骨细胞形成和破骨细胞最终形成所需基因的表达。在本研究中,我们研究了细胞-细胞相互作用对外周血单核细胞(PBMC)和人原发性牙周膜成纤维细胞培养物中黏附分子和参与破骨细胞形成的分子mRNA表达的影响,无论是作为单独培养还是作为联合培养-文化。我们进一步分析了多核抗酒石酸酸性磷酸酶(TRACP)阳性细胞的形成,并评估了它们的骨吸收能力。有趣的是,与单细胞培养相比,共培养中细胞间粘附分子1(ICAM-1)和破骨细胞生成相关基因(RANKL,RANK,TNF-α和IL-1β)的基因表达上调。培养和5-10倍的上调反映了由于直接的细胞间相互作用而产生的协同增加。这种诱导作用大大超过了已知的破骨细胞诱导剂I,25(OH)(2)VitD(3)和地塞米松的作用。在间接细胞-细胞接触的情况下,mRNA的表达没有改变,表明基因表达的增加需要异型粘附。此外,与单一培养相比,与牙周膜成纤维细胞共培养形成的破骨细胞样细胞数量明显增加。我们的数据表明破骨细胞前体和牙周膜成纤维细胞之间的细胞间粘附显着调节了细胞反应,从而有利于破骨细胞分化基因的表达和破骨细胞的最终形成。 J.细胞。生理。 222:565-573,2010。(C)2009 Wiley-Liss,Inc.

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