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Time evolution of microenvironment around cells regulated by the secretion activity and culture density of the cells

机译:细胞周围微环境的时间演变受细胞分泌活性和培养密度的调节

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Cells are the minimum unit of function for a living body. Cells are in a dynamic equilibrium state with mutually interacting with the microenvironment surrounding the cells. We focused on whether cellular responses also could be regulated in the interaction of cells with the other cells and/or the microenvironment of them. Here, we try to uncover the mechanism for the macrophages to acquire a stable response at the high cell density through simulations of the way for cell-cell communication via IFN-β. As a result, the extracellular concentration of IFN-β increased rapidly, and uniformly reached the effective concentration in any place in high-density culture condition. On the other hand, the local concentration of IFN-β in the low-density culture condition could rise transiently but easily decreased by diffusion, indicating that it was hard to reach the effective concentration in the most area. The cell density-dependent differences in IFN-β field formation were also shown to have a decisive effect on the stability of cellular responses from the population of cells. Collectively, we successfully demonstrated that the cells themselves dynamically form the surrounding microenvironment to regulate their own activity.
机译:细胞是生命体的最小功能单位。细胞处于动态平衡状态,与周围的微环境相互作用。我们关注于细胞应答是否也可以在细胞与其他细胞的相互作用和/或它们的微环境中被调节。在这里,我们尝试通过模拟通过IFN-β进行细胞间通讯的方式,揭示巨噬细胞在高细胞密度下获得稳定反应的机制。结果,IFN-β的细胞外浓度迅速增加,并且在高密度培养条件下的任何地方均均匀地达到有效浓度。另一方面,在低密度培养条件下,IFN-β的局部浓度可瞬时升高,但易于通过扩散而降低,这表明在大多数区域都难以达到有效浓度。还显示了IFN-β场形成中依赖于细胞密度的差异对来自细胞群的细胞反应的稳定性具有决定性作用。总的来说,我们成功地证明了细胞本身可以动态形成周围的微环境,从而调节自身的活动。

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