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当今的定量病理学——技术视角

Quantitative pathology today--a technical view.

作者信息

Baak J P

出版信息

Pathol Res Pract. 1987 Jun;182(3):396-400. doi: 10.1016/S0344-0338(87)80076-6.

Abstract

This paper gives an overview of the different techniques which are currently used in quantitative pathology. Morphometry is used to denote the interactive quantitative analysis of single cells or tissue sections by means of an eyepiece graticule, a projection microscope or a graphic tablet. It is a simple, inexpensive, relatively fast technique, and allows the quantitation of both cell and architectural (tissue) properties. Standard cell and tissue preparations can be employed for such investigations. This requires (minimal) standardization of the cell and tissue handling process. The degree of acidity (pH) of the fixation fluid, such as "neutral" (or buffered) formalin is probably the most important and easy to measure factor, and should be kept between 6 and 8 in order to obtain reproducible nuclear area measurements. Another important factor for reproducible results is the magnification in relation to the size of the particles measured. Careful selection of relevant areas, cells and nuclei done by a skilled pathologist, is often essential, as well as quality control of the measuring process. In static cytometry, a relatively popular application is the measurement of the DNA content of single cells in slides. Although having the advantage of optical control, the measuring technique of the transmission systems is, at the present state of development, laborious. This restricts the measurable number of cells to one hundred or only a few hundred at maximum. As a result, the reproducibility rate, as well as the capacity to detect small differences is only moderate.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本文概述了目前定量病理学中使用的不同技术。形态计量学用于通过目镜测微尺、投影显微镜或图形输入板对单细胞或组织切片进行交互式定量分析。它是一种简单、廉价、相对快速的技术,可对细胞和结构(组织)特性进行定量。此类研究可采用标准的细胞和组织标本。这需要对细胞和组织处理过程进行(最低限度的)标准化。固定液的酸度(pH值),如“中性”(或缓冲)福尔马林,可能是最重要且易于测量的因素,为获得可重复的核面积测量结果,其应保持在6至8之间。获得可重复结果的另一个重要因素是与所测颗粒大小相关的放大倍数。由熟练的病理学家仔细选择相关区域、细胞和细胞核通常至关重要,测量过程的质量控制也同样重要。在静态细胞计数中,一个相对流行的应用是测量载玻片上单细胞的DNA含量。尽管具有光学控制的优势,但在目前的发展状态下,透射系统的测量技术很繁琐。这将可测量的细胞数量限制在最多一百个或仅几百个。因此,重现率以及检测微小差异的能力仅处于中等水平。(摘要截选至250字)

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