首页> 美国卫生研究院文献>PLoS Clinical Trials >A Microfluidic-Based Multi-Shear Device for Investigating the Effects of Low Fluid-Induced Stresses on Osteoblasts
【2h】

A Microfluidic-Based Multi-Shear Device for Investigating the Effects of Low Fluid-Induced Stresses on Osteoblasts

机译:基于微流控的多剪切装置,用于研究低流体诱导的应力对成骨细胞的影响

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

Interstitial fluid flow (IFF) within the extracellular matrix (ECM) produces low magnitude shear stresses on cells. Fluid flow-induced stress (FSS) plays an important role during tissue morphogenesis. To investigate the effect of low FSS generated by IFF on cells, we developed a microfluidic-based cell culture device that can generate multiple low shear stresses. By changing the length and width of the flow-in channels, different continuous low level shear stresses could be generated in individual cell culture chambers. Numerical calculations demonstrate uniform shear stress distributions of the major cell culture area of each chamber. This calculation is further confirmed by the wall shear stress curves. The effects of low FSS on MC3T3-E1 proliferation and differentiation were studied using this device. It was found that FSS ranging from 1.5 to 52.6 µPa promoted MC3T3-E1 proliferation and differentiation, but FSS over 412 µPa inhibited the proliferation and differentiation of MC3T3-E1 cells. FSS ranging from 1.5 to 52.6 µPa also increased the expression of Runx2, a key transcription factor regulating osteoblast differentiation. It is suggested that Runx2 might be an important regulator in low FSS-induced MC3T3-E1 differentiation. This device allows for detailed study of the effect of low FSS on the behaviors of cells; thus, it would be a useful tool for analysis of the effects of IFF-induced shear stresses on cells.
机译:细胞外基质(ECM)中的间质液流(IFF)在细胞上产生较小的剪切应力。流体流动引起的应力(FSS)在组织形态发生过程中起重要作用。为了研究IFF产生的低FSS对细胞的影响,我们开发了一种基于微流体的细胞培养装置,该装置可以产生多个低剪切应力。通过改变流入通道的长度和宽度,可以在各个细胞培养室中产生不同的连续低水平剪切应力。数值计算表明,每个腔室的主要细胞培养区域的剪切应力分布均匀。壁剪应力曲线进一步证实了这一计算。使用该设备研究了低FSS对MC3T3-E1增殖和分化的影响。发现FSS在1.5至52.6 µPa之间可促进MC3T3-E1的增殖和分化,而FSS在412 µPa以上可抑制MC3T3-E1细胞的增殖和分化。 FSS范围从1.5到52.6 µPa也增加了Runx2的表达,Runx2是调节成骨细胞分化的关键转录因子。提示Runx2可能是低FSS诱导的MC3T3-E1分化的重要调控因子。该设备可以详细研究低FSS对细胞行为的影响;因此,它将是分析IFF诱导的剪应力对细胞影响的有用工具。

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