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Strain rate-dependent induction of reactive astrogliosis and cell death in three-dimensional neuronal-astrocytic co-cultures

机译:在三维神经元-星形胶质细胞共培养物中应变速率依赖性诱导反应性星形胶质细胞增生和细胞死亡

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摘要

A mechanical insult to the brain drastically alters the microenvironment as specific cell types become reactive in an effort to sequester severely damaged tissue. Although injury-induced astrogliosis has been investigated, the relationship between well-defined biomechanical inputs and acute astrogliotic alterations are not well understood. We evaluated the effects of strain rate on cell death and astrogliosis using a three-dimensional (3-D) in vitro model of neurons and astrocytes within a bioactive matrix. At 21 days post-plating, co-cultures were deformed to 0.50 shear strain at strain rates of 1, 10, or 30 s−1. We found that cell death and astrogliotic profiles varied differentially based on strain rate at two days post-insult. Significant cell death was observed after moderate (10 s−1) and high (30 s−1) rate deformation, but not after quasi-static (1 s−1) loading. The vast majority of cell death occurred in neurons, suggesting these cells are more susceptible to high rate shear strains than astrocytes for the insult parameters used here. Injury-induced astrogliosis was compared to co-cultures treated with transforming growth factor β, which induced robust astrocyte hypertrophy and increased glial fibrillary acidic protein (GFAP) and chondroitin-sulfate proteoglycans (CSPGs). Quasi-static loading resulted in increased cell density and CSPG secretion. Moderate rate deformation increased cell density, GFAP reactivity, and hypertrophic process density. High rate deformation resulted in increased GFAP reactivity; however, other astrogliotic alterations were not observed at this time-point. These results demonstrate that the mode and degree of astrogliosis depend on rate of deformation, demonstrating astrogliotic augmentation at sub-lethal injury levels as well as levels inducing cell death.
机译:当特定的细胞类型开始反应以隔离严重受损的组织时,对大脑的机械侮辱极大地改变了微环境。尽管已经研究了损伤引起的星形胶质细胞增生,但是对良好定义的生物力学输入和急性星形胶质细胞增生改变之间的关系还没有很好的了解。我们使用生物活性基质内的神经元和星形胶质细胞的三维(3-D)体外模型评估了应变速率对细胞死亡和星形胶质细胞增生的影响。接种后第21天,共培养物以1、10或30 s -1 的应变速率变形至0.50剪切应变。我们发现,在损伤后两天,细胞死亡和星形胶质细胞分布因应变率而异。在中等(10 s -1 )和高(30 s -1 )速率变形后观察到明显的细胞死亡,但在准静态(1 s −1 )加载。绝大多数细胞死亡发生在神经元中,这表明对于此处使用的损伤参数,这些细胞比星形胶质细胞更易受到高速率剪切应变的影响。将伤害诱导的星形胶质细胞增生与转化生长因子β处理的共培养进行了比较,转化生长因子β诱导了强烈的星形胶质细胞肥大,并增加了胶质纤维酸性蛋白(GFAP)和硫酸软骨素蛋白聚糖(CSPG)。准静态加载导致细胞密度和CSPG分泌增加。中度变形会增加细胞密度,GFAP反应性和肥大过程密度。高速率变形导致GFAP反应性增加;但是,在这个时间点没有观察到其他星形胶质变种。这些结果表明,星形胶质细胞增生的方式和程度取决于变形率,表明在亚致死损伤水平以及诱导细胞死亡的水平上星形胶质细胞增生。

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