Gschwendtner A, Mairinger T
Department of Pathology, University of Innsbruck, Austria.
Anal Cell Pathol. 1995 Jul;9(1):29-37.
The exact determination of the thickness of paraffin sections used for DNA cytometry on histological slides is an inevitable prerequisite to obtain reliable and reproducible results. Although section thickness can be measured with great precision and accuracy using highly specialized equipment (e.g. confocal laser microscope, microinterferometer), their cost restricts availability for many laboratories. This paper describes a simple method to determine the actual thickness of routinely processed paraffin sections used for DNA cytometry employing standard laboratory equipment. To achieve this goal the given section is divided into two parts. One part is used for DNA quantitation whereas the other is re-embedded and resectioned orthogonally through its original thickness. The thickness of the re-embedded section can now easily be determined with any standard length measurement device available in light microscopy. Recalculation of the genuine DNA-content out of the measured fractioned nuclei with commercial software based on the section thickness determined by this method generated histograms with a 2c equivalent peak, whereas correction based on the microtome settings resulted in significant deviations as demonstrated on rat liver tissue.
准确测定用于组织学切片DNA细胞计数的石蜡切片厚度,是获得可靠且可重复结果的必要前提。尽管使用高度专业化设备(如共聚焦激光显微镜、微干涉仪)能够高精度、高准确度地测量切片厚度,但设备成本限制了许多实验室的使用。本文介绍一种利用标准实验室设备测定用于DNA细胞计数的常规处理石蜡切片实际厚度的简单方法。为实现这一目标,将给定切片分为两部分。一部分用于DNA定量,另一部分重新包埋并沿其原始厚度正交切片。现在,使用光学显微镜中任何可用的标准长度测量设备,都能轻松测定重新包埋切片的厚度。基于此方法确定的切片厚度,利用商业软件从测量的部分细胞核中重新计算真实DNA含量,生成了具有2c等效峰的直方图,而基于切片机设置进行校正则导致显著偏差,如在大鼠肝脏组织上所示。