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使用“DEP”技术评估粘着斑激酶磷酸化与细胞黏附力的相关性。

Evaluation of the correlation between focal adhesion kinase phosphorylation and cell adhesion force using "DEP" technology.

机构信息

Department of Biomechatronic Engineering, National Chiayi University, No. 300, University Road, East District, Chiayi 600, Taiwan.

出版信息

Sensors (Basel). 2012;12(5):5951-65. doi: 10.3390/s120505951. Epub 2012 May 8.

Abstract

Dielectrophoresis (DEP) is the phenomenon in which a particle, such as a living cell, is polarized and moved by electrical gravity in a non-uniform electric field. In the present study, the DEP force is utilized to act on the cells to induce spatial movement for investigating the correlation between the cell adhesion force and activation level of focal adhesion kinase (FAK). The DEP force produced by the non-uniform electric field was used to measure the cell adhesion force of ECV304 cells, on type 1 collagen (COL1)- and fibronectin (FN)-coated polydimethylsiloxane (PDMS) membranes. For COL1-coating, ECV304 cells revealed weak and variable adhesion force (0.343-0.760 nN) in the first eight hours of incubation. Interestingly, the cell adhesion force of ECV304 at two and five hours of cultivation was significantly high and matched their FAK activation level. In comparison, ECV304 on FN-coated membrane had higher and more stable cell adhesion force (0.577-2.053 nN). FN coating intensified the cell adhesion force of ECV304 with culture time and similar outcome was present on the activation level of FAK. Therefore, this study demonstrated a relationship between cell adhesion force and FAK activation level that was dependent on the choice of the extracellular matrix (ECM) component. Subsequently, two tyrosine kinase inhibitors (AG18 and genistein) and one PI3K inhibitor (LY294002) were applied to study the influence of protein phosphorylation on the cell adhesion force. FAK plays an important role on cell attachment and DEP force measurement is a useful technique for studying cell adhesion.

摘要

介电泳(DEP)是一种现象,其中颗粒,如活细胞,被极化并在非均匀电场中通过电引力移动。在本研究中,利用DEP 力作用于细胞以诱导空间运动,研究细胞黏附力与粘着斑激酶(FAK)的激活水平之间的相关性。非均匀电场产生的 DEP 力用于测量 ECV304 细胞在 1 型胶原(COL1)和纤维连接蛋白(FN)涂覆的聚二甲基硅氧烷(PDMS)膜上的细胞黏附力。对于 COL1 涂层,ECV304 细胞在孵育的前 8 小时显示出弱且可变的黏附力(0.343-0.760 nN)。有趣的是,ECV304 在培养 2 和 5 小时的细胞黏附力明显较高,并与其 FAK 激活水平相匹配。相比之下,ECV304 在 FN 涂层膜上具有更高且更稳定的细胞黏附力(0.577-2.053 nN)。FN 涂层随培养时间增强了 ECV304 的细胞黏附力,FAK 的激活水平也存在类似的结果。因此,本研究表明细胞黏附力与 FAK 激活水平之间存在关系,这取决于细胞外基质(ECM)成分的选择。随后,应用两种酪氨酸激酶抑制剂(AG18 和金雀异黄素)和一种 PI3K 抑制剂(LY294002)来研究蛋白质磷酸化对细胞黏附力的影响。FAK 在细胞附着中起重要作用,DEP 力测量是研究细胞黏附的有用技术。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df2f/3386723/9f6eb074cf55/sensors-12-05951f1.jpg

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