Department of Cell Biology, Physiology and Immunology, Universitat Autònoma de Barcelona, 08193 Bellaterra, Spain.
Int J Mol Sci. 2013 Jul 30;14(8):15810-26. doi: 10.3390/ijms140815810.
Phosphorylation of the H2AX protein is an early step in the double strand break (DSB) repair pathway; therefore, phosphorylated histone (γH2AX) foci scoring is widely used as a measure for DSBs. Foci scoring is performed either manually or semi-automatically using hand-operated capturing and image analysis software. In general, both techniques are laborious and prone to artifacts associated with manual scoring. While a few fully automated methods have been described in the literature, none of them have been used to quantify γH2AX foci in combination with a cell cycle phase analysis. Adding this feature to a rapid automated γH2AX foci quantification method would reduce the scoring uncertainty that arises from the variations in the background level of the γH2AX signal throughout the cell cycle. The method was set up to measure DNA damage induced in human mammary epithelial cells by irradiation under a mammogram device. We adapted a FISH (fluorescent in situ hybridization) Spot-counting system, which has a slide loader with automatic scanning and cell capture system throughout the thickness of each cell (z-stack), to meet our assay requirements. While scanning the sample, the system classifies the selected nuclei according to the signal patterns previously described by the user. For our purposes, a double staining immunofluorescence was carried out with antibodies to detect γH2AX and pericentrin, an integral component of the centrosome. We could thus distinguish both the number of γH2AX foci per cell and the cell cycle phase. Furthermore, restrictive settings of the program classifier reduced the "touching nuclei" problem described in other image analysis software. The automated scoring was faster than and as sensitive as its manually performed counterpart. This system is a reliable tool for γH2AX radio-induced foci counting and provides essential information about the cell cycle stage. It thus offers a more complete and rapid assessment of DNA damage.
磷酸化 H2AX 蛋白是双链断裂 (DSB) 修复途径的早期步骤;因此,磷酸化组蛋白 (γH2AX) 焦点评分被广泛用作 DSB 的测量方法。焦点评分可以手动或半自动进行,使用手动捕获和图像分析软件。一般来说,这两种技术都很繁琐,并且容易出现与手动评分相关的伪影。虽然文献中已经描述了几种全自动方法,但没有一种方法用于与细胞周期相分析相结合来定量 γH2AX 焦点。将此功能添加到快速自动化的 γH2AX 焦点定量方法中,可以减少由于整个细胞周期中 γH2AX 信号背景水平的变化而导致的评分不确定性。该方法是为了测量在 mammogram 设备下照射诱导的人乳腺上皮细胞中的 DNA 损伤而建立的。我们适应了 FISH(荧光原位杂交)点计数系统,该系统具有带有自动扫描和细胞捕获系统的载玻片加载器,可以对每个细胞(z 堆栈)的整个厚度进行扫描,以满足我们的测定要求。在扫描样品时,系统会根据用户先前描述的信号模式对选定的核进行分类。对于我们的目的,进行了双重染色免疫荧光,使用针对 γH2AX 和中心体的组成部分中心体蛋白的抗体进行检测。因此,我们可以区分每个细胞中的 γH2AX 焦点数量和细胞周期相。此外,程序分类器的限制设置减少了其他图像分析软件中描述的“接触核”问题。自动化评分比手动评分更快且更敏感。该系统是用于 γH2AX 放射性诱导焦点计数的可靠工具,并提供有关细胞周期阶段的重要信息。因此,它提供了对 DNA 损伤的更完整和快速评估。