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单细胞分辨率下细胞群体通过受限空间的趋化运动。

Chemotaxis of cell populations through confined spaces at single-cell resolution.

机构信息

Department of Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, Maryland, United States of America.

出版信息

PLoS One. 2012;7(1):e29211. doi: 10.1371/journal.pone.0029211. Epub 2012 Jan 18.

Abstract

Cell migration is crucial for both physiological and pathological processes. Current in vitro cell motility assays suffer from various drawbacks, including insufficient temporal and/or optical resolution, or the failure to include a controlled chemotactic stimulus. Here, we address these limitations with a migration chamber that utilizes a self-sustaining chemotactic gradient to induce locomotion through confined environments that emulate physiological settings. Dynamic real-time analysis of both population-scale and single-cell movement are achieved at high resolution. Interior surfaces can be functionalized through adsorption of extracellular matrix components, and pharmacological agents can be administered to cells directly, or indirectly through the chemotactic reservoir. Direct comparison of multiple cell types can be achieved in a single enclosed system to compare inherent migratory potentials. Our novel microfluidic design is therefore a powerful tool for the study of cellular chemotaxis, and is suitable for a wide range of biological and biomedical applications.

摘要

细胞迁移对于生理和病理过程都至关重要。目前的体外细胞迁移分析存在多种缺陷,包括时间和/或光学分辨率不足,或者无法提供受控的趋化刺激。在这里,我们使用一种自维持趋化梯度的迁移室来解决这些限制,该迁移室可在模拟生理环境的受限环境中诱导运动。可以以高分辨率动态实时分析群体规模和单细胞运动。通过吸附细胞外基质成分可以对内部表面进行功能化,并且可以直接向细胞或通过趋化剂库间接给予药理学试剂。可以在单个封闭系统中直接比较多种细胞类型,以比较固有迁移潜力。因此,我们的新型微流控设计是研究细胞趋化性的有力工具,适用于广泛的生物学和生物医学应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b00/3261140/46d7ece87134/pone.0029211.g001.jpg

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