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The effect of polyurethane scaffold surface treatments on the adhesion of chondrocytes subjected to interstitial perfusion culture

机译:聚氨酯支架表面处理对间质灌注培养软骨细胞黏附的影响

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摘要

The purpose of this study was to measure chondrocytes detachment from cellularized constructs cultured in a perfusion bioreactor, and to evaluate the effect of different scaffold coatings on cell adhesion under a fixed flow rate. The scaffolds were polyurethane foams, treated to promote cell attachment and seeded with human chondrocytes. In a preliminary static culture experiment, the scaffolds were imbibed with fetal bovine serum (FBS) and then cultured for 4 weeks. To quantify cell detachment, the number of detached cells from the scaffold treated with FBS was estimated under different interstitial perfusion flow rates and shear stress levels (0.005 mL/min equivalent to 0.05 mPa, 0.023 mL/min equivalent to 0.23 mPa, and 0.045 mL/min equivalent to 0.45 mPa). Finally, groups of scaffolds differently treated (FBS, plasma plus FBS, plasma plus collagen type I) were cultured under a fixed perfusion rate of 0.009 mL/min, equivalent to a shear stress of 0.09 mPa, and the detached cells were counted. Static cultivation showed that cell proliferation increased with time and matrix biosynthesis decreased after the first week of culture. Perfused culture showed that the number of detached cells increased with the perfusion rate on FBS-treated constructs. The plasma-treated/collagen-coated scaffolds showed the highest resistance to cell detachment. To minimize cell detachment, the perfusion rate must be maintained in the order of 0.02 mL/min, giving a shear stress of 0.2 mPa. Our set-up allowed estimating the resistance to cell detachment under interstitial perfusion in a repeatable manner, to test other scaffold coatings and cell types.
机译:这项研究的目的是测量从灌注生物反应器中培养的细胞结构中分离的软骨细胞,并评估固定流速下不同支架涂层对细胞粘附的影响。支架是聚氨酯泡沫,经处理可促进细胞附着并接种人软骨细胞。在初步的静态培养实验中,将支架吸收胎牛血清(FBS),然后培养4周。为了量化细胞分离,在不同的间质灌注流速和剪切应力水平(0.005 mL / min相当于0.05 mPa,0.023 mL / min相当于0.23 mPa和0.045 mL)下,估算了用FBS处理的支架中脱离的细胞数量。 / min等于0.45 mPa)。最后,将不同处理的支架组(FBS,血浆加FBS,血浆加I型胶原)以0.009 mL / min的固定灌注速率(相当于0.09 mPa的切应力)进行培养,并对分离的细胞进行计数。静态培养表明,培养的第一周后,细胞增殖随时间增加而基质生物合成减少。灌注培养表明,在FBS处理的构建体上,分离细胞的数量随灌注速率的增加而增加。血浆处理/胶原涂层的支架显示出最高的细胞分离抗性。为了最大程度地减少细胞分离,灌注速率必须保持在0.02 mL / min的数量级,剪切应力为0.2 mPa。我们的设置允许以可重复的方式估计组织间灌注下细胞分离的抵抗力,以测试其他支架涂层和细胞类型。

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