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一种用于低细胞数量样本制备以进行透射电子显微镜分析的替代方法。

An Alternative Approach for Sample Preparation with Low Cell Number for TEM Analysis.

作者信息

Kumar Sachin, Filippi Marie-Dominique

机构信息

Division of Experimental Hematology and Cancer Biology, Cincinnati Children's Research Foundation;

出版信息

J Vis Exp. 2016 Oct 12(116):54724. doi: 10.3791/54724.

DOI:10.3791/54724
PMID:27768053
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5092190/
Abstract

Transmission electron microscopy (TEM) provides details of the cellular organization and ultrastructure. However, TEM analysis of rare cell populations, especially cells in suspension such as hematopoietic stem cells (HSCs), remains limited due to the requirement of a high cell number during sample preparation. There are a few cytospin or monolayer approaches for TEM analysis from scarce samples, but these approaches fail to get significant quantitative data from the limited number of cells. Here, an alternative and novel approach for sample preparation in TEM studies is described for rare cell populations that enables quantitative analysis. A relatively low cell number, i.e., 10,000 HSCs, was successfully used for TEM analysis compared to the millions of cells typically used for TEM studies. In particular, Evans blue staining was performed after paraformaldehyde-glutaraldehyde (PFA-GA) fixation to visualize the tiny cell pellet, which facilitated embedding in agarose. Clusters of numerous cells were observed in ultra-thin sections. The cells had a well preserved morphology, and the ultra-structural details of the Golgi complex and several mitochondria were visible. This efficient, easy and reproducible protocol allows sample preparation from a low cell number and can be used for qualitative and quantitative TEM analysis on rare cell populations from limited biological samples.

摘要

透射电子显微镜(TEM)可提供细胞组织和超微结构的详细信息。然而,由于在样品制备过程中需要大量细胞,对稀有细胞群体(尤其是悬浮细胞,如造血干细胞(HSC))的TEM分析仍然有限。对于稀缺样品的TEM分析,有一些细胞涂片或单层制备方法,但这些方法无法从有限数量的细胞中获得有意义的定量数据。在此,本文描述了一种用于TEM研究的样品制备的替代新方法,该方法适用于稀有细胞群体,能够进行定量分析。与通常用于TEM研究的数百万个细胞相比,相对较少数量的细胞(即10,000个造血干细胞)成功用于TEM分析。特别是,在多聚甲醛-戊二醛(PFA-GA)固定后进行伊文思蓝染色,以可视化微小的细胞沉淀,这有助于将其包埋在琼脂糖中。在超薄切片中观察到大量细胞簇。细胞形态保存良好,高尔基体复合体和几个线粒体的超微结构细节清晰可见。这种高效、简便且可重复的方案允许从少量细胞制备样品,可用于对来自有限生物样品的稀有细胞群体进行定性和定量TEM分析。