首页> 美国卫生研究院文献>Biomedical Optics Express >Quantitative observations on cytoskeleton changes of osteocytes at different cell parts using digital holographic microscopy
【2h】

Quantitative observations on cytoskeleton changes of osteocytes at different cell parts using digital holographic microscopy

机译:利用数字全息显微镜对不同细胞部位骨细胞细胞骨架变化的定量观察

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Cytoskeletons such as F-actin have different distributions in different cell parts and they are the cause of different degrees of cell collapse when the F-actin is disrupted. It is challenging to use conventional methods such as fluorescence microscopy and atomic force microscopy to conduct real-time and three-dimensional observations on the dynamic processes at different cell parts due to the slow measuring speed and the need for live-cell staining. In this study, the morphological variations of different bone cell parts caused by F-actin disruption are dynamically measured by using digital holographic microscopy (DHM). We separately analyze local parameters (cell height and cell width) and global parameters (cell projected area and cell volume) of cells to address variations of specific cell areas and quantify the changing process of the whole cell. We found significant differences in temporal variations of both local and global cell parameters between the cell body and cell process, which is consistent with the qualitative observation by fluorescence staining. Our study not only validates the unique ability of DHM to simultaneously investigate the dynamic process at different cell parts, but also provides sufficient experimental bases for exploring the mechanism for F-actin disruption.
机译:诸如F-肌动蛋白之类的细胞骨架在不同细胞部位具有不同的分布,当F-肌动蛋白被破坏时,它们是造成不同程度细胞崩溃的原因。由于测量速度慢和需要活细胞染色,因此使用常规方法(例如荧光显微镜和原子力显微镜)对不同细胞部分的动态过程进行实时和三维观察是一项挑战。在这项研究中,通过使用数字全息显微镜(DHM)动态测量由F-肌动蛋白破坏引起的不同骨细胞部分的形态变化。我们分别分析单元格的局部参数(单元格高度和单元格宽度)和全局参数(单元格投影面积和单元格体积)以解决特定单元格区域的变化并量化整个单元格的变化过程。我们发现细胞体和细胞过程之间局部和全局细胞参数的时间变化存在显着差异,这与荧光染色的定性观察一致。我们的研究不仅验证了DHM能够同时研究不同细胞部分动态过程的独特能力,而且还为探索F-肌动蛋白破坏的机理提供了足够的实验基础。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号