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Optimum temperature for extracellular matrix production by articular chondrocytes

机译:关节软骨细胞产生细胞外基质的最佳温度

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Purpose: The purpose of this study was to investigate the influence of temperature on the ability of the chondrocytes to produce extracellular matrix (ECM). Materials and methods: Articular chondrocytes were isolated from porcine knee joints. The chondrocytes were cultured at three different temperatures: 32?°C, 37?°C, and 41?°C. The ability to produce ECM was assessed by gene expression analysis, histological, and biochemical evaluation in a pellet culture system. Results: Wet weight of the pellets generated after 21 days, was significantly heavier when cultured at lower temperatures. Picrosirius red staining, employed to evaluate collagen production, was higher at lower temperatures, and safranin-O staining, used to evaluate sulphated glycosaminoglycan (GAG), was lower at 32?°C than at 37?°C and 41?°C. Collagen type IIA1 mRNA expression was markedly up-regulated at 41?°C. However, picrosirius red staining was inhibited at 41?°C. GAG and DNA content were measured by 1,9-dimethylmethylene blue (DMMB) assay and PicoGreen? assay, respectively. The GAG content per pellet was significantly low at 41?°C compared to that at 32?°C and 37?°C. The DNA content per pellet was larger at lower temperatures. The GAG content normalised with the DNA content per pellet was significantly lower at 32?°C compared to that at 37?°C and 41?°C. Conclusion: Our results suggest that a culture temperature of approximately 41?°C inhibits ECM production by decreasing DNA content and perhaps by collagen misfolding. Taken together, the optimum temperature for ECM production in articular chondrocytes may be between 32?°C and 37?°C.
机译:目的:本研究的目的是研究温度对软骨细胞产生细胞外基质(ECM)能力的影响。材料和方法:从猪膝关节分离关节软骨细胞。软骨细胞在三种不同的温度下培养:32℃,37℃和41℃。通过基因表达分析,组织学和生化评估在颗粒培养系统中评估产生ECM的能力。结果:21天后产生的沉淀的湿重,在较低温度下培养时明显重。用于评估胶原蛋白生成的Picrosirius红色染色在较低温度下较高,而用于评估硫酸化糖胺聚糖(GAG)的番红O染色在32°C下低于37°C和41°C。 IIA1型胶原蛋白mRNA表达在41°C时明显上调。然而,在41℃下,苦橙红染色被抑制。 GAG和DNA含量通过1,9-二甲基亚甲基蓝(DMMB)测定和PicoGreen?化验。与32°C和37°C时相比,41°C下每粒颗粒的GAG含量明显较低。在较低温度下,每个沉淀的DNA含量较大。与每粒DNA含量标准化的GAG含量在32°C时明显低于37°C和41°C。结论:我们的结果表明,大约41°C的培养温度可通过降低DNA含量并可能通过胶原蛋白错误折叠来抑制ECM的产生。综上所述,关节软骨细胞中产生ECM的最佳温度可能在32°C至37°C之间。

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