首页> 美国卫生研究院文献>PLoS Clinical Trials >Ensemble Analysis of Angiogenic Growth in Three-Dimensional Microfluidic Cell Cultures
【2h】

Ensemble Analysis of Angiogenic Growth in Three-Dimensional Microfluidic Cell Cultures

机译:三维微流控细胞培养中血管生成的集合分析

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

We demonstrate ensemble three-dimensional cell cultures and quantitative analysis of angiogenic growth from uniform endothelial monolayers. Our approach combines two key elements: a micro-fluidic assay that enables parallelized angiogenic growth instances subject to common extracellular conditions, and an automated image acquisition and processing scheme enabling high-throughput, unbiased quantification of angiogenic growth. Because of the increased throughput of the assay in comparison to existing three-dimensional morphogenic assays, statistical properties of angiogenic growth can be reliably estimated. We used the assay to evaluate the combined effects of vascular endothelial growth factor (VEGF) and the signaling lipid sphingoshine-1-phosphate (S1P). Our results show the importance of S1P in amplifying the angiogenic response in the presence of VEGF gradients. Furthermore, the application of S1P with VEGF gradients resulted in angiogenic sprouts with higher aspect ratio than S1P with background levels of VEGF, despite reduced total migratory activity. This implies a synergistic effect between the growth factors in promoting angiogenic activity. Finally, the variance in the computed angiogenic metrics (as measured by ensemble standard deviation) was found to increase linearly with the ensemble mean. This finding is consistent with stochastic agent-based mathematical models of angiogenesis that represent angiogenic growth as a series of independent stochastic cell-level decisions.
机译:我们展示了整体三维细胞培养和血管内皮生长从均匀的内皮细胞单层的定量分析。我们的方法结合了两个关键要素:一种微流体测定法,使平行的血管生成生长实例能够经受常见的细胞外条件;以及一种自动化的图像采集和处理方案,能够对血管生成的生长进行高通量,无偏量化。由于与现有的三维形态发生测定相比,该测定的通量增加,因此可以可靠地估计血管生成生长的统计特性。我们使用该测定法评估了血管内皮生长因子(VEGF)和信号脂质鞘氨醇-1-磷酸(S1P)的联合作用。我们的结果表明,在存在VEGF梯度的情况下,S1P在放大血管生成反应中的重要性。此外,尽管总迁移活性降低,但具有VEGF梯度的S1P的应用却产生了长宽比比具有VEGF背景水平的S1P更高的血管生成芽。这暗示了生长因子之间在促进血管生成活性方面的协同作用。最后,发现计算出的血管生成指标的变化(以集合标准偏差衡量)随集合平均值线性增加。这一发现与血管生成的基于随机代理的数学模型相一致,该数学模型将血管生成的增长表示为一系列独立的随机细胞水平决策。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号