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The effect of mechanical loading on osteogenesis of human dental pulp stromal cells in a novel in vitro model.

机译:在新型体外模型中,机械负荷对人牙髓基质细胞成骨作用的影响。

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Tooth loss often results in alveolar bone resorption because of lack of mechanical stimulation. Thus, the mechanism of mechanical loading on stem cell osteogenesis is crucial for alveolar bone regeneration. We have investigated the effect of mechanical loading on osteogenesis in human dental pulp stromal cells (hDPSCs) in a novel in vitro model. Briefly, 1?×?10(7) hDPSCs were seeded into 1 ml 3% agarose gel in a 48-well-plate. A loading tube was then placed in the middle of the gel to mimic tooth-chewing movement (1 Hz, 3?×?30 min per day, n?=?3). A non-loading group was used as a control. At various time points, the distribution of live/dead cells within the gel was confirmed by fluorescence markers and confocal microscopy. The correlation and interaction between the factors (e.g. force, time, depth and distance) were statistically analysed. The samples were processed for histology and immunohistochemistry. After 1-3 weeks of culture in the in-house-designed in vitro bioreactor, fluorescence imaging confirmed that additional mechanical loading increased the viable cell numbers over time as compared with the control. Cells of various phenotypes formed different patterns away from the reaction tube. The cells in the middle part of the gel showed enhanced alkaline phosphatase staining at week 1 but reduced staining at weeks 2 and 3. Additional loading enhanced Sirius Red and type I collagen staining compared with the control. We have thus successfully developed a novel in-house-designed in vitro bioreactor mimicking the biting force to enhance hDPSC osteogenesis in an agarose scaffold and to promote bone formation and/or prevent bone resorption.
机译:由于缺乏机械刺激,牙齿脱落经常导致牙槽骨吸收。因此,机械负荷对干细胞成骨的机制对于牙槽骨再生至关重要。我们已经研究了在新型体外模型中机械负荷对人牙髓基质细胞(hDPSCs)成骨的影响。简而言之,将1×××10(7)hDPSCs接种到在48孔板中的1ml 3%琼脂糖凝胶中。然后将加载管置于凝胶的中间以模拟咀嚼牙齿的动作(1Hz,3××30分钟/天,n = 3)。非负荷组用作对照。在各个时间点,通过荧光标记和共聚焦显微镜证实了活/死细胞在凝胶内的分布。统计学分析了因素(例如力,时间,深度和距离)之间的相关性和相互作用。对样品进行组织学和免疫组织化学处理。在内部设计的体外生物反应器中培养1-3周后,荧光成像证实与对照相比,额外的机械负荷随时间的推移增加了活细胞数。各种表型的细胞远离反应管形成不同的模式。凝胶中部的细胞在第1周显示出增强的碱性磷酸酶染色,但在第2周和第3周显示出减少的染色。与对照相比,额外的负载增强了Sirius Red和I型胶原蛋白的染色。因此,我们成功地开发了一种新型的内部设计的体外生物反应器,该反应器可模仿咬合力,以增强琼脂糖支架中的hDPSC成骨作用并促进骨形成和/或防止骨吸收。

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