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Lithography-Free Fabrication of Reconfigurable Substrate Topography For Contact Guidance

机译:用于接触引导的可重构衬底形貌的无光刻制造

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摘要

Mammalian cells detect and respond to topographical cues presented in natural and synthetic biomaterials both in vivo and in vitro. Micro- and nano-structures influence the adhesion, morphology, proliferation, migration, and differentiation of many phenotypes. Although the mechanisms that underpin cell-topography interactions remain elusive, synthetic substrates with well-defined micro- and nano-structures are important tools to elucidate the origin of these responses. Substrates with reconfigurable topography are desirable because programmable cues can be harmonized with dynamic cellular responses. Here we present a lithography-free fabrication technique that can reversibly present topographical cues using an actuation mechanism that minimizes the confounding effects of applied stimuli. This method utilizes strain-induced buckling instabilities in bi-layer substrate materials with rigid uniform silicon oxide membranes that are thermally deposited on elastomeric substrates. The resulting surfaces are capable of reversible of substrates between three distinct states: flat substrates (A = 1.53 ± 0.55 nm, Rms = 0.317 ± 0.048 nm); parallel wavy grating arrays (A|| = 483.6 ± 7.8 nm and λ|| = 4.78 ± 0.16 μm); perpendicular wavy grating arrays (A⊥ = 429.3 ± 5.8 nm; λ⊥ = 4.95 ± 0.36 μm). The cytoskeleton dynamics of 3T3 fibroblasts in response to these surfaces was measured using optical microscopy. Fibroblasts cultured on dynamic substrates that are switched from flat to topographic features (FLAT-WAVY) exhibit a robust and rapid change in gross morphology as measured by a reduction in circularity from 0.30 ± 0.13 to 0.15 ± 0.08 after 5 min. Conversely, dynamic substrate sequences of FLAT-WAVY-FLAT do not significantly alter the gross steady-state morphology. Taken together, substrates that present topographic structures reversibly can elucidate dynamic aspects of cell-topography interactions.
机译:哺乳动物细胞可在体内和体外检测天然和合成生物材料中呈现的地形线索并对其做出反应。微观和纳米结构影响许多表型的粘附,形态,增殖,迁移和分化。尽管支撑细胞-拓扑学相互作用的机制仍然难以捉摸,但具有明确的微观和纳米结构的合成底物是阐明这些反应起源的重要工具。具有可重构形貌的基板是可取的,因为可以将可编程提示与动态细胞响应相协调。在这里,我们提出了一种无需光刻的制造技术,该技术可以使用一种使所施加刺激的混杂效应最小化的致动机制来可逆地呈现地形线索。该方法利用了具有刚性均匀的氧化硅膜的双层基底材料中的应变诱导的屈曲不稳定性,该材料均匀地沉积在弹性体基底上。所得的表面能够在三种不同状态之间使基板可逆:平坦基板(A = 1.53±0.55 nm,Rms = 0.317±0.048 nm);平行波浪光栅阵列(A || = 483.6±7.8 nm和λ|| = 4.78±0.16μm);垂直波状光栅阵列(A⊥= 429.3±5.8 nm;λ⊥= 4.95±0.36μm)。使用光学显微镜测量响应这些表面的3T3成纤维细胞的细胞骨架动力学。通过在5分钟后将圆度从0.30±0.13降低到0.15±0.08来测量,在从平坦特征转换为地形特征(FLAT-WAVY)的动态基质上培养的成纤维细胞显示出强大,快速的总体形态变化。相反,FLAT-WAVY-FLAT的动态底物序列不会显着改变总体稳态形态。两者合计,可逆地呈现拓扑结构的底物可以阐明细胞-拓扑交互作用的动态方面。

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