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聚氨酯支架表面处理对经间隙灌注培养的软骨细胞黏附的影响。

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

作者信息

Raimondi Manuela Teresa, Bertoldi Serena, Caddeo Silvia, Farè Silvia, Arrigoni Chiara, Moretti Matteo

机构信息

1Department of Chemistry, Materials and Chemical Engineering "G. Natta", Politecnico di Milano, Milano, Italy.

5Department of Chemistry, Materials and Chemical Engineering "G. Natta", Politecnico di Milano, Piazza L. da Vinci 32, Milano, 20133 Italy.

出版信息

Tissue Eng Regen Med. 2016 Aug 5;13(4):364-374. doi: 10.1007/s13770-016-9047-8. eCollection 2016 Aug.

Abstract

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.

摘要

本研究的目的是测量在灌注生物反应器中培养的细胞化构建体上软骨细胞的脱离情况,并评估在固定流速下不同支架涂层对细胞黏附的影响。支架为聚氨酯泡沫,经过处理以促进细胞黏附,并接种人软骨细胞。在初步的静态培养实验中,将支架用胎牛血清(FBS)浸润,然后培养4周。为了量化细胞脱离,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、0.045 mL/min相当于0.45 mPa)下,估计用FBS处理的支架上脱离细胞的数量。最后,将不同处理的支架组(FBS、血浆加FBS、血浆加I型胶原)在0.009 mL/min的固定灌注速率下培养,相当于0.09 mPa的剪切应力,并对脱离细胞进行计数。静态培养表明,细胞增殖随时间增加,而基质生物合成在培养第一周后下降。灌注培养表明,在FBS处理的构建体上,脱离细胞的数量随灌注速率增加。经血浆处理/胶原包被的支架对细胞脱离表现出最高的抗性。为了使细胞脱离最小化,灌注速率必须保持在0.02 mL/min左右,产生0.2 mPa的剪切应力。我们的装置能够以可重复的方式估计间质灌注下对细胞脱离的抗性,以测试其他支架涂层和细胞类型。

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