通过安装用于激光显微解剖的组织切片来提高分辨率。

M C R F van Dijk, P D M Rombout, H B P M Dijkman, D J Ruiter, M R Bernsen
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引用次数: 18

摘要

背景:激光微束显微解剖极大地促进了从组织切片中获得特定细胞群。然而,不使用复盖的事实意味着组织切片的形态学往往很差。目的:研究一种能大大提高激光微束显微解剖组织切片形态学质量的安装方法,以便于靶细胞的鉴定。方法:采用新鲜冷冻组织和福尔马林固定、石蜡包埋组织标本,检测挂载组织和未挂载组织的形态学质量。安装溶液由胶粘胶和稀释在水中的蓝色墨水组成。通过显微解剖从挂载和未挂载的组织中分离10-2000个细胞,用聚合酶链反应分析挂载液对DNA质量的干扰。结果:载片液能明显改善激光显微解剖组织切片的形态,对DNA的分离和扩增效率无不利影响。缺点之一是安装溶液降低了紫外激光器的切割效率。为了尽量减少这种影响,安装溶液应尽可能稀释。此外,在安装介质中添加蓝色墨水可以恢复激光器的切割效率。结论:该试剂盒制备简便,易于应用,可与多种染色方法联合使用,且不影响提取DNA的质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Improved resolution by mounting of tissue sections for laser microdissection.

Background: Laser microbeam microdissection has greatly facilitated the procurement of specific cell populations from tissue sections. However, the fact that a coverslip is not used means that the morphology of the tissue sections is often poor.

Aims: To develop a mounting method that greatly improves the morphological quality of tissue sections for laser microbeam microdissection purposes so that the identification of target cells can be facilitated.

Methods: Fresh frozen tissue and formalin fixed, paraffin wax embedded tissue specimens were used to test the morphological quality of mounted and unmounted tissue. The mounting solution consisted of an adhesive gum and blue ink diluted in water. Interference of the mounting solution with DNA quality was analysed by the polymerase chain reaction using 10-2000 cells isolated by microdissection from mounted and unmounted tissue.

Results: The mounting solution greatly improved the morphology of tissue sections for laser microdissection purposes and had no detrimental effects on the isolation and efficiency of amplification of DNA. One disadvantage was that the mounting solution reduced the cutting efficiency of the ultraviolet laser. To minimise this effect, the mounting solution should be diluted as much as possible. Furthermore, the addition of blue ink to the mounting medium restores the cutting efficiency of the laser.

Conclusions: The mounting solution is easy to prepare and apply and can be combined with various staining methods without compromising the quality of the DNA extracted.

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