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当前细胞微图案化技术的比较研究与改进

Comparative study and improvement of current cell micro-patterning techniques.

作者信息

Fink Jenny, Théry Manuel, Azioune Ammar, Dupont Raphael, Chatelain François, Bornens Michel, Piel Matthieu

机构信息

Biologie du cycle cellulaire et de la motilité, Institut Curie, CNRS, UMR144, 26 rue d'Ulm, 75005 Paris, France.

出版信息

Lab Chip. 2007 Jun;7(6):672-80. doi: 10.1039/b618545b. Epub 2007 Apr 30.

Abstract

The original micropatterning technique on gold, although very efficient, is not accessible to most biology labs and is not compatible with their techniques for image acquisition. Other solutions have been developed on silanized glass coverslips. These methods are still hardly accessible to biology labs and do not provide sufficient reproducibility to become incorporated in routine biological protocols. Here, we analyzed cell behavior on micro-patterns produced by various alternative techniques. Distinct cell types displayed different behavior on micropatterns, while some were easily constrained by the patterns others escaped or ripped off the patterned adhesion molecules. We report methods to overcome some of these limitations on glass coverslips and on plastic dishes which are compatible with our experimental biological applications. Finally, we present a new method based on UV crosslinking of adhesion proteins with benzophenone to easily and rapidly produce highly reproducible micropatterns without the use of a microfabricated elastomeric stamp.

摘要

最初在金表面进行微图案化的技术,尽管效率很高,但大多数生物实验室无法使用,且与它们的图像采集技术不兼容。在硅烷化玻璃盖玻片上已开发出其他解决方案。这些方法生物实验室仍然很难使用,并且没有提供足够的可重复性以纳入常规生物学实验方案。在这里,我们分析了通过各种替代技术产生的微图案上的细胞行为。不同的细胞类型在微图案上表现出不同的行为,一些细胞很容易受到图案的限制,而另一些则逃脱或扯下了图案化的粘附分子。我们报告了一些方法来克服在玻璃盖玻片和塑料培养皿上的这些限制,这些方法与我们的实验生物学应用兼容。最后,我们提出了一种基于粘附蛋白与二苯甲酮进行紫外交联的新方法,无需使用微加工弹性印章即可轻松快速地产生高度可重复的微图案。

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