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首页> 外文期刊>ChemNanoMat >Convenient, Reliable, Bias-Free Dynamic Patterning of Multiple Types of Cells into Precisely Defined Micropatterns for Co-Culture Study
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Convenient, Reliable, Bias-Free Dynamic Patterning of Multiple Types of Cells into Precisely Defined Micropatterns for Co-Culture Study

机译:方便,可靠,无偏差的将多种类型的细胞动态图案化为用于共同培养研究的精确定义的微模式

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摘要

We present a simple and flexible mechanical approach for 2D micropatterning of multiple cell lines without surface modification. The principle is that during initial attachment cells only stick to unoccupied areas; we create such areas to selectively seed a subsequent cell line by using a stamp to erase previously attached cells at designed areas. By repeating this process, multiple types of cells were patterned on a single substrate. This strategy minimizes the disturbance to cell health, which might be a concern in printing-based patterning. Micropatterns of cells with resolution of ?≈ 50 μm, and a co-culture of three cell types were easily achieved and studied. This method was found universal to at least MSC, HeLa, HepG2 and NIH 3T3. We also measured the invasion and cell growth under the co-culture of HeLa, MSC and HepG2. This method is useful for studying cell-cell interaction in high-throughput, free of the potential bias caused by selective surface modification in some previous methods.
机译:我们提出了一种简单灵活的机械方法,无需表面修饰即可对多个细胞系进行2D微图案化。原理是,在初始附着期间,牢房仅粘附在未被占用的区域上。我们创建这样的区域,以通过使用图章擦除设计区域的先前附着的细胞来选择性地接种后续的细胞系。通过重复此过程,可以在单个基板上对多种类型的单元进行构图。这种策略可以最大程度地减少对细胞健康的干扰,而这可能是基于打印的图案形成中的一个问题。容易实现并研究分辨率为≈≈50μm的细胞的微模式以及三种细胞类型的共培养。发现该方法至少对于MSC,HeLa,HepG2和NIH 3T3通用。我们还测量了HeLa,MSC和HepG2共同培养下的侵袭和细胞生长。该方法对于研究高通量的细胞间相互作用非常有用,而不会因某些先前方法中的选择性表面修饰而引起潜在的偏倚。

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