3.8 Article

Geometric Control of Cell Behavior by Biomolecule Nanodistribution

期刊

ACS BIOMATERIALS SCIENCE & ENGINEERING
卷 8, 期 11, 页码 4789-4806

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsbiomaterials.2c00650

关键词

nanopatterning; nanospacing; biornimetic surface; electron-beam lithography; cell-cell interaction; cell adhesion and spreading; ligand clustering

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Dynamic interactions within the cell micro-environment have significant impacts on cell behavior and fate, however, pathways and mechanisms of cell-cell or cell-extracellular matrix interactions at the nanoscale level are still understudied. Recent advancements in nanotechnology, particularly electron-beam lithography (EBL), offer the ability to mimic microenvironments at the nanoscale in vitro, providing insights into cellular signaling mechanisms.
Many dynamic interactions within the cell micro-environment modulate cell behavior and cell fate. However, the pathways and mechanisms behind cell-cell or cell-extracellular matrix interactions remain understudied, as they occur at a nanoscale level. Recent progress in nanotechnology allows for mimicking of the microenvironment at nanoscale in vitro; electron-beam lithography (EBL) is currently the most promising technique. Although this nanopatterning technique can generate nanostructures of good quality and resolution, it has resulted, thus far, in the production of only simple shapes (e.g., rectangles) over a relatively small area (100 x 100 mu m), leaving its potential in biological applications unfulfilled. Here, we used EBL for cell-interaction studies by coating cell-culture-relevant material with electron-conductive indium tin oxide, which formed nanopatterns of complex nanohexagonal structures over a large area (500 x 500 mu m). We confirmed the potential of EBL for use in cell-interaction studies by analyzing specific cell responses toward differentially distributed nanohexagons spaced at 1000, 500, and 250 nm. We found that our optimized technique of EBL with HaloTags enabled the investigation of broad changes to a cell-culture-relevant surface and can provide an understanding of cellular signaling mechanisms at a single-molecule level.

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