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首页> 外文期刊>Biomechanics and modeling in mechanobiology >Cyclic hydrostatic compression stimulates chondroinduction of C3H/10T1/2 cells
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Cyclic hydrostatic compression stimulates chondroinduction of C3H/10T1/2 cells

机译:循环静水压缩刺激C3H / 10T1 / 2细胞的软骨诱导

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摘要

While the potential for intermittent hydrostatic pressure to promote cartilaginous matrix synthesis is well established, its potential to influence chondroinduction remains poorly understood. This study examined the effects of relatively short- and long-duration cyclic hydrostatic compression on the chondroinduction of C3H/10T1/2 murine embryonic fibroblasts by recombinant human bone morphogenetic protein-2 (rhBMP-2). Cells were seeded at high density into round bottom wells of a 96-well plate and supplemented with 25 ng/ml rhBMP-2. Experimental cultures were subjected to either 1,800 cycles/day or 7,200 cycles/day of 1 Hz sinusoidal hydrostatic compression to 5 MPa (applied 10 min on/10 min off) for 3 days. Non-pressurized control and experimental cultures were maintained in static culture for an additional 5 days. Cultures were then analyzed for alcian blue staining intensity, DNA and sulfated glycosaminoglycan (sGAG) content, and for the rate of collagen synthesis. Whereas cultures subjected to 1,800 pressure cycles exhibited no significant differences (statistical or qualitative) compared to controls, those subjected to 7,200 cycles stained more intensely with alcian blue, contained nearly twice as much sGAG, and displayed twice the rate of collagen synthesis as non-pressurized controls. This study demonstrates the potential for cyclic hydrostatic compression to stimulate chondrogenic differentiation of the C3H/10T1/2 cell line in a duration-dependent manner.
机译:虽然间歇性静水压力促进软骨基质合成的潜力已得到充分确立,但其影响软骨诱导的潜力仍知之甚少。这项研究检查了相对较短和较长时间的循环静水压缩对重组人骨形态发生蛋白2(rhBMP-2)对C3H / 10T1 / 2鼠胚胎成纤维细胞软骨诱导的影响。将细胞以高密度接种到96孔板的圆底孔中,并补充25 ng / ml rhBMP-2。对实验培养物进行1 800次/天或7200次/天的1 Hz正弦静水压至5 MPa(施加10分钟开启/关闭10分钟关闭),持续3天。非加压对照和实验培养物在静态培养物中再维持5天。然后分析培养物的阿尔辛蓝染色强度,DNA和硫酸化的糖胺聚糖(sGAG)含量,以及胶原蛋白的合成速率。与对照相比,经过1800个压力循环的培养物没有表现出显着差异(统计或定性),而经过7200个循环的培养物用阿尔辛蓝染色更深,sGAG含量几乎是后者的两倍,并且胶原蛋白合成速率是非胶原蛋白的两倍。加压控制。这项研究表明循环静水压缩以持续时间依赖的方式刺激C3H / 10T1 / 2细胞系软骨分化的潜力。

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