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利用中子反射技术理解活细胞黏附的动态变化。

Understanding dynamic changes in live cell adhesion with neutron reflectometry.

作者信息

Junghans Ann, Waltman Mary Jo, Smith Hillary L, Pocivavsek Luka, Zebda Noureddine, Birukov Konstantin, Viapiano Mariano, Majewski Jaroslaw

机构信息

MPA-CINT/Lujan Neutron Scattering Center, Los Alamos Neutron Science Center, Los Alamos National Laboratory, Los Alamos, New Mexico, 87545, USA.

Biosciences Division, Bioenergy and Biome Sciences, Los Alamos National Laboratory, Los Alamos, New Mexico, 87545, USA.

出版信息

Mod Phys Lett B. 2014 Dec 10;28(30). doi: 10.1142/S0217984914300154.

Abstract

Neutron reflectometry (NR) was used to examine various live cells adhesion to quartz substrates under different environmental conditions, including flow stress. To the best of our knowledge, these measurements represent the first successful visualization and quantization of the interface between live cells and a substrate with sub-nanometer resolution. In our first experiments, we examined live mouse fibroblast cells as opposed to past experiments using supported lipids, proteins, or peptide layers with no associated cells. We continued the NR studies of cell adhesion by investigating endothelial monolayers and glioblastoma cells under dynamic flow conditions. We demonstrated that neutron reflectometry is a powerful tool to study the strength of cellular layer adhesion in living tissues, which is a key factor in understanding the physiology of cell interactions and conditions leading to abnormal or disease circumstances. Continuative measurements, such as investigating changes in tumor cell - surface contact of various glioblastomas, could impact advancements in tumor treatments. In principle, this can help us to identify changes that correlate with tumor invasiveness. Pursuit of these studies can have significant medical impact on the understanding of complex biological problems and their effective treatment, for the development of targeted anti-invasive therapies.

摘要

中子反射测量技术(NR)被用于研究在包括流动应力在内的不同环境条件下,各种活细胞与石英基底的粘附情况。据我们所知,这些测量首次成功地以亚纳米分辨率对活细胞与基底之间的界面进行了可视化和量化。在我们的首次实验中,我们研究的是活的小鼠成纤维细胞,而过去的实验使用的是没有相关细胞的支持脂质、蛋白质或肽层。我们通过研究动态流动条件下的内皮单层细胞和胶质母细胞瘤细胞,继续进行细胞粘附的NR研究。我们证明,中子反射测量技术是研究活组织中细胞层粘附强度的有力工具,而这是理解细胞相互作用生理过程以及导致异常或疾病情况的条件的关键因素。连续测量,比如研究各种胶质母细胞瘤肿瘤细胞 - 表面接触的变化,可能会影响肿瘤治疗的进展。原则上,这可以帮助我们识别与肿瘤侵袭性相关的变化。开展这些研究对理解复杂生物学问题及其有效治疗具有重大医学意义,有助于开发靶向抗侵袭疗法。

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