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MICROFLUIDIC DEVICES AS IN-VITRO MICROENVIRONMENTS FOR STEM CELL CULTURE

机译:微流体装置作为干细胞培养的体外微环境

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Many potential therapies are currently being studied that may promote neural regeneration and guide regenerating axons to form correct connections following injury. It has been shown that adult neurons have some limited regenerative capabilities, and the lack of connection formation between neurons is not an intrinsic inability of these cells to form axons after being damaged, but rather the inhibitory microenvironment of the injured tissue prevents regeneration. In this study, the polarization and chemotaxis of neuronal stem cells (NSC) in response to quantified gradients of nerve growth factor (NGF) was examined. To accomplish this, a microfluidic device was designed and fabricated to generate stable concentration gradients of biomolecules in a cell culture chamber within a 3D microenvironment. Numerical simulation was implemented to optimize the device geometry for generating a uniform concentration gradient of NGF which was found to remain stable for multiple hours. NSCs migration was studied within this microfluidic device in response to NGF concentration and within a 3D environment of collagen matrix. This device is expected to have wide applicability in the study of shear-sensitive cells such as NSC and non-adherent cell types as well as in the study of migration through three dimensional matrices.
机译:目前正在研究许多潜在的疗法,这可能促进神经再生和引导再生轴突,以形成损伤后的正确连接。已经表明,成年神经元具有一些有限的再生能力,并且神经元之间的连接形成不是这些细胞在损坏后形成轴突的内在不能形成轴突,而是受伤组织的抑制微环境可防止再生。在该研究中,检查了神经元干细胞(NSC)的偏振和趋化响应于神经生长因子(NGF)的量化梯度。为了实现这一点,设计了一种微流体装置并制造,以在3D微环境中产生细胞培养室中的生物分子的稳定浓度梯度。实施了数值模拟以优化用于产生NGF的均匀浓度梯度的装置几何形状,发现发现多小时保持稳定。在该微流体装置中研究了NSCs迁移,响应于NGF浓度和胶原蛋白基质的3D环境内。该装置预计在研究剪切敏感细胞如NSC和非依赖细胞类型的研究中具有广泛的适用性,以及通过三维矩阵迁移的研究。

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