[ Objective ] The aim was to investigate the influence of flow rate on the phagocytosis ability of cells on fiuorescent silicon ddoxide microsphere [ Method ] The cells were cultured on self-made micro-fluidic microehip for researching the endocytosis function of cells on silicon dioxide microsphcrc in flowing state. [ Result ] In the microscopic images. the control cells emitted intease red light, indicating that there were a large number of si1icon dioxide microparticles in them: the cells enltured in the channel were transmitting silicon dioxide microparticles in flowing sate, their fluorescence inlensily was lower than that of control group and decreasing along with the increase of flow rate in channel.showing that the intake amount of cells on silicon dioxide was decreased in flowing state. With cells co-cultured with silicon dioxide microparticles for 6 h in call bottle as control group, wetting their fluorescence intensily as 100 ％, when the flow rate of liquid stream in micro channel was increased from 0.023 mm/s to 0.079 mm/s, its fluorescence intensity was decreased from 51.2％ to 28.2％, indicating that the phagorytosis amount of cells on silicon dioxide microparticles was decreased obviously along with the increase of flow rate. [ Conclusion ] This experimant provided a new method for researching the endocytosis function of cellls.%[目的]考察流速对细胞吞噬二氧化硅荧光微球能力的影响.[方法]在自制微流控芯片上进行细胞培养以研究流动状态下细胞对二氧化硅微球的胞吞性能、[结果]显微镜照片显示,对照细胞发出强烈的红光,表明细胞吞噬了大量的二氧化硅微粒;在通道中培养的细胞在流动状态下传输二氧化硅微粒,其荧光强度比对照组低,随着通道内流速增大,其荧光强度下降,表明流动状态下细胞对二氧化硅的摄入量降低.以在细胞瓶中与二氧化硅微粒共培养6h后的细胞为对照组,以其荧光强度为100%,微通道中液流流速从0.023mm/s增加到0.079 mm/s时,荧光强度从51.2%下降到28.2%,表明随着流速的增加,细胞对二氧化硅微球的吞噬量明显下降.[结论]该实验为研究细胞的胞吞性能提供了新方法.
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