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A SIMPLE ASPECT RATIO DEPENDENT METHOD OF PATTERNING MICROWELLS FOR SELECTIVE CELL ATTACHMENT

机译:一种简单的纵横比依赖性方法,用于选择性细胞附着的图案化微孔

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3-D culture has been shown to provide cells with a more physiologically authentic environment than traditional 2-D (planar) culture [1, 2]. 3-D cues allow cells to exhibit more realistic functions and behaviors, e.g., adhesion, spreading, migration, metabolic activity, and differentiation. Knowledge of changes in cell morphology, mechanics, and mobility in response to geometrical cues and topological stimuli is important for understanding normal and pathological cell development [3] Microfabrication provides unique in vitro approaches to recapitulating in vivo conditions due to the ability to precisely control the cellular microenvironment [4, 5] Microwell arrays have emerged as robust alternatives to traditional 2-D cell culture substrates as they are relatively simple and compatible with existing laboratory techniques and instrumentation [6, 7]. In particular, microwells have been adopted as a biomimetic approach to modeling the unique micro-architecture of the epithelial lining of the gastrointestinal (GI) tract [8-10]. The inner (lumen-facing) surface of the intestine has a convoluted topography consisting of finger-like projections (villi) with deep well-like invaginations (crypts) between them. The dimensions of villi and crypts are on the order of hundreds of microns (100-700 μm in height and 50-250 μm in diameter) [11] While microwells have proven important in the development of physiologically realistic in vitro models of human intestine, existing methods of ensuring their surface is suitable for cell culture are lacking. Sometimes it is desirable to selectively seed cells within microwells and confine or restrict them to the microwells in which they are seeded. Existing methods of patterning microwells for cell attachment either lack selectivity, meaning cells can adhere and migrate anywhere on the microwell array, i.e., inside microwells or outside of them, or necessitate sophisticated techniques such as micro-contact printing, which requires precise alignment and control to selectively pattern the bottoms of microwells for cell attachment [12, 13].
机译:已显示3-D培养物提供比传统的2-D(平面)培养物更具生理的真实环境的细胞[1,2]。 3-D提示允许细胞表现出更现实的功能和行为,例如粘附,传播,迁移,代谢活性和分化。了解细胞形态,力学和流动性的变化,响应几何线索和拓扑刺激对于了解正常和病理细胞发育非常重要[3]微生物可提供独特的体外方法,因为精确控制的能力提供了体内条件的重新制作的方法细胞微环境[4,5]微孔阵列已经出现为传统的2-D细胞培养基材的鲁棒替代品,因为它们相对简单,与现有的实验室技术和仪器相兼容[6,7]。特别地,已经采用微孔作为模拟胃肠道(GI)道的上皮衬里的独特微架构的仿生方法[8-10]。肠道的内(腔腔)表面具有由具有双重良好的凸起(绒毛)组成的复杂的地形,它们之间是深度良好的invininations(隐窝)。 Villi和Crypts的尺寸是数百微米(高度为100-700μm,直径为50-250μm)[11],而Microwells在生理上真实的人类肠道的发展中经过遗憾,确保其表面的现有方法适用于细胞培养。有时希望选择性地将细胞在微孔中和限制或限制它们播种的微孔。用于细胞连接的图案化微孔的现有方法缺乏选择性,含义电池可以粘附和迁移微孔阵列的任何位置,即在微孔中或其外部,或者需要进行复杂的技术,例如微接触印刷,这需要精确的对准和控制选择性地模式微孔的微孔底部[12,13]。

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