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本文引用的文献

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Artificial niche microarrays for probing single stem cell fate in high throughput.高通量探测单个干细胞命运的人工小生境微阵列。
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Spatial control of cell fate using synthetic surfaces to potentiate TGF-beta signaling.利用合成表面进行细胞命运的空间控制,以增强 TGF-β 信号。
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Cantilever-free scanning probe molecular printing.无悬臂扫描探针分子印刷
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Nanolithographic control of the spatial organization of cellular adhesion receptors at the single-molecule level.纳米光刻技术在单分子水平上控制细胞黏附受体的空间组织。
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Nanotechnological strategies for engineering complex tissues.纳米技术在复杂组织工程中的策略。
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Biomimetic nanopatterns as enabling tools for analysis and control of live cells.仿生纳米图案作为分析和控制活细胞的有效工具。
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Combinatorial development of biomaterials for clonal growth of human pluripotent stem cells.组合开发用于人类多能干细胞克隆生长的生物材料。
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Geometric cues for directing the differentiation of mesenchymal stem cells.用于指导间充质干细胞分化的几何线索。
Proc Natl Acad Sci U S A. 2010 Mar 16;107(11):4872-7. doi: 10.1073/pnas.0903269107. Epub 2010 Mar 1.
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"Force-feedback" leveling of massively parallel arrays in polymer pen lithography.聚合物笔式光刻中大规模并行阵列的力反馈调平。
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扫描探针使能的纳米组合定义了纤连蛋白特征尺寸与干细胞命运之间的关系。

Scanning probe-enabled nanocombinatorics define the relationship between fibronectin feature size and stem cell fate.

机构信息

Department of Materials Science and Engineering, Northwestern University,2145 Sheridan Road, Evanston, IL 60208, USA.

出版信息

Proc Natl Acad Sci U S A. 2012 Mar 20;109(12):4377-82. doi: 10.1073/pnas.1201086109. Epub 2012 Mar 5.

DOI:10.1073/pnas.1201086109
PMID:22392973
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3311369/
Abstract

We report the development of a powerful analytical method that utilizes a tilted elastomeric pyramidal pen array in the context of a scanning probe lithography experiment to rapidly prepare libraries having as many as 25 million features over large areas with a range of feature sizes from the nano- to microscale. This technique can be used to probe important chemical and biological processes, opening up the field of nanocombinatorics. In a proof-of-concept investigation of mesenchymal stem cell (MSC) differentiation, combinatorial patterns first enabled a rapid and systematic screening of MSC adhesion, as a function of feature size, while uniform patterns were used to study differentiation with statistically significant sample sizes. Without media containing osteogenic-inducing chemical cues, cells cultured on nanopatterned fibronectin substrates direct MSC differentiation towards osteogenic fates when compared to nonpatterned fibronectin substrates. This powerful and versatile approach enables studies of many systems spanning biology, chemistry, and engineering areas.

摘要

我们开发了一种强大的分析方法,该方法在扫描探针光刻实验中利用倾斜的弹性金字塔笔阵列,可快速制备具有多达 2500 万个特征的文库,特征尺寸范围从纳米到微米级。这项技术可用于探测重要的化学和生物学过程,开辟了纳米组合学领域。在对间充质干细胞(MSC)分化的概念验证研究中,组合图案首先能够快速系统地筛选 MSC 黏附,作为特征尺寸的函数,而均匀图案则用于研究具有统计学显着样本量的分化。与非图案化纤连蛋白底物相比,在不含成骨诱导化学信号的培养基中,培养在纳米图案化纤连蛋白底物上的细胞会促使 MSC 向成骨命运分化。这种强大且多功能的方法可以用于研究生物学、化学和工程领域的许多系统。