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通过安装用于激光显微切割的组织切片提高分辨率。

Improved resolution by mounting of tissue sections for laser microdissection.

作者信息

van Dijk M C R F, Rombout P D M, Dijkman H B P M, Ruiter D J, Bernsen M R

机构信息

Department of Pathology, University Medical Centre Nijmegen, PO Box 9101, 6500 HB Nijmegen, The Netherlands.

出版信息

Mol Pathol. 2003 Aug;56(4):240-3. doi: 10.1136/mp.56.4.240.

Abstract

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.

摘要

背景

激光微束显微切割极大地促进了从组织切片中获取特定细胞群体的过程。然而,不使用盖玻片这一事实意味着组织切片的形态往往较差。

目的

开发一种封固方法,以显著提高用于激光微束显微切割的组织切片的形态质量,从而便于识别靶细胞。

方法

使用新鲜冷冻组织以及经福尔马林固定、石蜡包埋的组织标本,来测试封固和未封固组织的形态质量。封固液由一种粘性树胶和稀释于水中的蓝色墨水组成。通过聚合酶链反应,使用从封固和未封固组织中经显微切割分离出的10 - 2000个细胞,分析封固液对DNA质量的干扰。

结果

封固液极大地改善了用于激光微束显微切割的组织切片的形态,且对DNA的分离和扩增效率没有不利影响。一个缺点是封固液降低了紫外激光的切割效率。为使这种影响最小化,封固液应尽可能稀释。此外,在封固介质中添加蓝色墨水可恢复激光的切割效率。

结论

封固液易于制备和应用,并且可以与各种染色方法相结合,而不会损害所提取DNA的质量。

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