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Growth characterization of neo porcine cartilage pellets and their use in an interactive culture model.

机译:新猪软骨颗粒的生长特性及其在交互式培养模型中的应用。

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OBJECTIVE: The aim of this study was to evaluate the growth characteristics of freshly isolated porcine chondrocytes in high-density pellet cultures and to preliminary investigate their use in an interactive in vitro model with synovial fibroblast cell lines to study rheumatoid arthritis (RA). DESIGN: 1.8x10(6) chondrocytes/cm2 were seeded in 48-multiwell plates. Thickness, cell number and cell distribution in pellet cross sections were documented over a 22-day-long period. Alcian blue staining, type I and type II collagen staining, real-time reverse transcriptase polymerase polymerase chain reaction (RT-PCR) and high performance liquid chromatography (HPLC) were used to characterize cartilage extracellular matrix (ECM) formation, and cell proliferation was demonstrated by Ki67 staining. Furthermore, 2-week-old chondrocyte pellets were co-cultured for additional 2 weeks with two human synovial fibroblast cell lines derived from a normal donor (non-invasive cell line) and a RA patient (invasive-aggressive (IA) cell line), respectively. RESULTS: Chondrocyte pellets from 11 individual preparations showed a significant increase in pellet thickness from 44+/-19 microm (day 3) to 282+/-19 microm (day 22). Calculation of chondrocyte distribution, cell number and pellet thickness indicated that pellet growth was due to ECM formation and not cell proliferation. This was also confirmed by low numbers of Ki67 positive chondrocytes and absence of cell clusters. HPLC, messenger RNA-analysis, histochemistry and antibody staining verified the expression of ECM components such as type II collagen, whereas type I collagen expression was very low. In contrast to the non-aggressive synovial fibroblast cell line, the IA synovial fibroblast cell line clearly showed cartilage invasion. CONCLUSION: Pellet formation of freshly isolated chondrocytes followed a reproducible developmental kinetics and showed typical immature hyaline cartilage properties. Such uniform cartilage pellets are very useful as a substratefor interactive cell culture models that simulate diseases like RA.
机译:目的:本研究旨在评估新鲜分离的猪软骨细胞在高密度颗粒培养物中的生长特性,并初步研究其在滑膜成纤维细胞系相互作用的体外模型中用于研究类风湿关节炎(RA)的用途。设计:将1.8x10(6)软骨细胞/ cm2接种在48孔板中。在22天的时间内记录了丸粒横截面的厚度,孔数和孔分布。使用Alcian蓝染色,I型和II型胶原蛋白染色,实时逆转录聚合酶聚合酶链反应(RT-PCR)和高效液相色谱(HPLC)来表征软骨细胞外基质(ECM)的形成,并且细胞增殖Ki67染色证明。此外,将2周龄的软骨细胞沉淀与衍生自正常供体(非侵入性细胞系)和RA患者(侵入性(IA)细胞系)的两种人滑膜成纤维细胞系共培养另外2周。 , 分别。结果:11种单独制剂的软骨细胞沉淀显示出沉淀厚度从44 +/- 19微米(第3天)显着增加到282 +/- 19微米(第22天)。软骨细胞分布,细胞数量和沉淀厚度的计算表明沉淀生长是由于ECM形成而不是细胞增殖。 Ki67阳性软骨细胞数量少和缺乏细胞簇也证实了这一点。 HPLC,信使RNA分析,组织化学和抗体染色证实了ECM成分例如II型胶原的表达,而I型胶原的表达非常低。与非侵袭性滑膜成纤维细胞系相反,IA滑膜成纤维细胞系清楚地显示出软骨侵袭。结论:新鲜分离的软骨细胞的团粒形成遵循可再现的发育动力学,并表现出典型的不透明透明软骨特性。这种均匀的软骨沉淀物非常有用,可作为模拟RA等疾病的交互式细胞培养模型的底物。

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