首页> 美国卫生研究院文献>Bioengineering >3D Cell Migration Studies for Chemotaxis on Microfluidic-Based Chips: A Comparison between Cardiac and Dermal Fibroblasts
【2h】

3D Cell Migration Studies for Chemotaxis on Microfluidic-Based Chips: A Comparison between Cardiac and Dermal Fibroblasts

机译:基于微流体芯片的趋化性的3D细胞迁移研究:心脏和真皮成纤维细胞之间的比较。

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

Fibroblast migration to damaged zones in different tissues is crucial to regenerate and recuperate their functional activity. However, fibroblast migration patterns have hardly been studied in disease terms. Here, we study this fundamental process in dermal and cardiac fibroblasts by means of microfluidic-based experiments, which simulate a three-dimensional matrix in which fibroblasts are found in physiological conditions. Cardiac fibroblasts show a higher mean and effective speed, as well as greater contractile force, in comparison to dermal fibroblasts. In addition, we generate chemical gradients to study fibroblast response to platelet derived growth factor (PDGF) and transforming growth factor beta (TGF-β) gradients. Dermal fibroblasts were attracted to PDGF, whereas cardiac fibroblasts are not. Notwithstanding, cardiac fibroblasts increased their mean and effective velocity in the presence of TGF-β. Therefore, given that we observe that the application of these growth factors does not modify fibroblasts’ morphology, these alterations in the migration patterns may be due to an intracellular regulation.
机译:成纤维细胞迁移到不同组织的受损区域对于再生和恢复其功能活性至关重要。然而,很少从疾病角度研究成纤维细胞迁移模式。在这里,我们通过基于微流体的实验研究了真皮和心脏成纤维细胞中的这一基本过程,该实验模拟了在生理条件下发现成纤维细胞的三维矩阵。与真皮成纤维细胞相比,心脏成纤维细胞显示出更高的平均速度和有效速度,以及更大的收缩力。此外,我们生成化学梯度以研究成纤维细胞对血小板衍生生长因子(PDGF)和转化生长因子β(TGF-β)梯度的反应。真皮成纤维细胞被PDGF吸引,而心脏成纤维细胞则没有。尽管如此,在存在TGF-β的情况下,心脏成纤维细胞增加了其平均速度和有效速度。因此,考虑到我们观察到这些生长因子的应用不会改变成纤维细胞的形态,因此迁移模式的这些改变可能是由于细胞内调控所致。

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