首页> 外文期刊>International Journal of Clinical and Experimental Pathology >Co-culture with periodontal ligament stem cells enhanced osteoblastic differentiation of MC3T3-E1 cells and osteoclastic differentiation of RAW264.7 cells
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Co-culture with periodontal ligament stem cells enhanced osteoblastic differentiation of MC3T3-E1 cells and osteoclastic differentiation of RAW264.7 cells

机译:与牙周膜干细胞共培养可增强MC3T3-E1细胞的成骨细胞分化和RAW264.7细胞的破骨细胞分化

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Objectives: Periodontal ligament stem cells (PDLSCs) are characterized by having multipotential differentiation and immunoregulatory properties, which are the main mechanisms of PDLSCs-mediated periodontal regeneration. Periodontal or bone regeneration requires coordination of osteoblast and osteoclast, however, very little is known about the interactions between PDLSCs and osteoblast-like cells or osteoclast precursors. In this study, the indirect co-culture approach was introduced to preliminarily elucidate the effects of PDLSCs on differentiation of osteoblast-like cells and osteoclast precursors in vitro. Materials and methods: Human PDLSCs were obtained from premolars extracted and their stemness was identified in terms of their colony-forming ability, proliferative capacity, cell surface epitopes and multi-lineage differentiation potentials. A noncontact co-culture system of PDLSCs and preosteoblastic cell line MC3T3-E1 or osteoclast precursor cell line RAW264.7 was established, and osteoblastic differentiation of MC3T3-E1 and osteoclastic differentiation of RAW264.7 were evaluated. Results: PDLSCs exhibited features of mesenchymal stem cells. Further investigation through indirect co-culture system showed that PDLSCs enhanced ALP activity, expressions of ALP, Runx2, BSP, OPN mRNA and BSP, OPN proteins and mineralization matrix deposition in MC3T3-E1. Meanwhile, they improved maturation of osteoclasts and expressions of TRAP, CSTK, TRAF6 mRNA and TRAP, TRAF6 proteins in RAW264.7. Conclusions: PDLSCs stimulates osteoblastic differentiation of osteoblast precursors and osteoclastic differentiation of osteoclast precursors, at least partially, in a paracrine fasion.
机译:目的:牙周膜干细胞(PDLSCs)具有多能分化和免疫调节特性,这是PDLSCs介导的牙周再生的主要机制。牙周或骨骼再生需要协调成骨细胞和破骨细胞,但是,关于PDLSC与成骨细胞样细胞或破骨细胞前体之间的相互作用了解甚少。在这项研究中,引入了间接共培养方法,以初步阐明PDLSC在体外对成骨样细胞和破骨细胞前体分化的影响。材料和方法:从提取的前磨牙获得人PDLSC,并根据其菌落形成能力,增殖能力,细胞表面表位和多谱系分化潜能鉴定其干性。建立了PDLSC与成骨前细胞细胞系MC3T3-E1或破骨细胞前体细胞RAW264.7的非接触共培养系统,并评估了MC3T3-E1的成骨细胞分化和RAW264.7的破骨细胞分化。结果:PDLSCs具有间充质干细胞的特征。通过间接共培养系统的进一步研究表明,PDLSCs增强了ALP活性,ALP,Runx2,BSP,OPN mRNA和BSP,OPN蛋白的表达以及在MC3T3-E1中的矿化基质沉积。同时,它们改善了破骨细胞的成熟以及RAW264.7中TRAP,CSTK,TRAF6 mRNA和TRAP,TRAF6蛋白的表达。结论:PDLSCs至少部分地在旁分泌因子中刺激成骨细胞前体的成骨细胞分化和破骨细胞前体的破骨细胞分化。

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