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使用表面等离子体共振成像椭圆测量法研究细胞-基质黏附动力学。

Study of cell-matrix adhesion dynamics using surface plasmon resonance imaging ellipsometry.

机构信息

Center for Nano-Bio Convergence Research, Korea Research Institute of Standards and Science, Daejeon, Republic of Korea.

出版信息

Biophys J. 2011 Apr 6;100(7):1819-28. doi: 10.1016/j.bpj.2011.01.033.

DOI:10.1016/j.bpj.2011.01.033
PMID:21463596
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3072622/
Abstract

The interaction of cells with extracellular matrix, termed cell-matrix adhesions, importantly governs multiple cellular phenomena. Knowledge of the functional dynamics of cell-matrix adhesion could provide critical clues for understanding biological phenomena. We developed surface plasmon resonance imaging ellipsometry (SPRIE) to provide high contrast images of the cell-matrix interface in unlabeled living cells. To improve the contrast and sensitivity, the null-type imaging ellipsometry technique was integrated with an attenuated total reflection coupler. We verified that the imaged area of SPRIE was indeed a cell-matrix adhesion area by confocal microscopy imaging. Using SPRIE, we demonstrated that three different cell types exhibit distinct features of adhesion. SPRIE was applied to diverse biological systems, including during cell division, cell migration, and cell-cell communication. We imaged the cell-matrix anchorage of mitotic cells, providing the first label-free imaging of this interaction to our knowledge. We found that cell-cell communication can alter cell-matrix adhesion, possibly providing direct experimental evidence for cell-cell communication-mediated changes in cell adhesion. We also investigated shear-stress-induced adhesion dynamics in real time. Based on these data, we expect that SPRIE will be a useful methodology for studying the role of cell-matrix adhesion in important biological phenomena.

摘要

细胞与细胞外基质的相互作用,称为细胞-基质黏附,对多种细胞现象具有重要意义。了解细胞-基质黏附的功能动力学可以为理解生物学现象提供关键线索。我们开发了表面等离子体共振成像椭圆偏光术(SPRIE),以提供未经标记的活细胞中细胞-基质界面的高对比度图像。为了提高对比度和灵敏度,我们将消光型成像椭圆偏光术技术与衰减全反射耦合器集成在一起。我们通过共聚焦显微镜成像验证了 SPRIE 成像区域确实是细胞-基质黏附区域。使用 SPRIE,我们证明了三种不同的细胞类型表现出不同的黏附特征。SPRIE 被应用于多种生物系统,包括细胞分裂、细胞迁移和细胞间通讯。我们对有丝分裂细胞的细胞-基质锚定进行了成像,据我们所知,这是对这种相互作用的首次无标记成像。我们发现细胞间通讯可以改变细胞-基质黏附,这可能为细胞间通讯介导的细胞黏附变化提供直接的实验证据。我们还实时研究了剪切力诱导的黏附动力学。基于这些数据,我们预计 SPRIE 将成为研究细胞-基质黏附在重要生物学现象中作用的有用方法。

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本文引用的文献

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Mouse fibroblast cell adhesion studied by neutron reflectometry.利用中子反射技术研究鼠成纤维细胞黏附。
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Total internal reflection fluorescence microscopy of cell adhesion on patterned self-assembled monolayers on gold.金表面图案化自组装单分子层上细胞黏附的全内反射荧光显微镜观察
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Surface plasmon resonance imaging of cells and surface-associated fibronectin.细胞与表面相关纤连蛋白的表面等离子体共振成像
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Surface plasmon resonance sensors for detection of chemical and biological species.用于检测化学和生物物质的表面等离子体共振传感器。
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Cell-matrix adhesion.细胞-基质黏附
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Cell shape and cell division.细胞形状与细胞分裂。
Curr Opin Cell Biol. 2006 Dec;18(6):648-57. doi: 10.1016/j.ceb.2006.10.001. Epub 2006 Oct 12.