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Hydrostatic pressure-generated reactive oxygen species induce osteoarthritic conditions in cartilage pellet cultures

机译:静水压力产生的活性氧物种在软骨颗粒培养物中诱导骨关节炎条件

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Osteoarthritis (OA) is one of the most common causes of disability and represents a major socio-economic burden. Despite intensive research, the molecular mechanisms responsible for the initiation and progression of OA remain inconclusive. In recent years experimental findings revealed elevated levels of reactive oxygen species (ROS) as a major factor contributing to the onset and progression of OA. Hence, we designed a hydrostatic pressure bioreactor system that is capable of stimulating cartilage cell cultures with elevated ROS levels. Increased ROS levels in the media did not only lead to an inhibition of glycosaminoglycans and collagen II formation but also to a reduction of already formed glycosaminoglycans and collagen II in chondrogenic mesenchymal stem cell pellet cultures. These effects were associated with the elevated activity of matrix metalloproteinases as well as the increased expression of several inflammatory cytokines. ROS activated different signaling pathways including PI3K/Akt and MAPK/ERK which are known to be involved in OA initiation and progression. Utilizing the presented bioreactor system, an OA in vitro model based on the generation of ROS was developed that enables the further investigation of ROS effects on cartilage degradation but can also be used as a versatile tool for anti-oxidative drug testing.
机译:骨关节炎(OA)是残疾最常见的原因之一,代表了一个主要的社会经济负担。尽管研究密集研究,负责OA的启动和进展的分子机制仍然不确定。近年来,实验结果揭示了活性氧物种(ROS)水平升高,作为有助于OA的发作和进展的主要因素。因此,我们设计了一种静水压力生物反应器系统,其能够刺激具有升高的ROS水平的软骨细胞培养物。培养基中的ROS水平增加不仅导致血糖素聚糖和胶原蛋白二糖基因组的抑制,而且还抑制已在软骨间充质干细胞颗粒颗粒颗粒颗粒颗粒颗粒培养物中已经形成的已经形成的糖胺聚糖和胶原II。这些效应与基质金属蛋白酶的升高相关以及几种炎性细胞因子的增加的表达。 ROS激活了不同的信令路径,包括PI3K / AKT和MAPK / ERK,已知参与OA启动和进展。利用所提出的生物反应器系统,开发了一种基于ROS产生的OA体外模型,可以进一步调查ROS对软骨降解的影响,但也可以用作抗氧化药物测试的多功能工具。

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