Department of Pathology, Central Finland Central Hospital, Keskussairaalantie 19, 40620 Jyväskylä, Finland.
Exp Mol Pathol. 2010 Apr;88(2):265-71. doi: 10.1016/j.yexmp.2009.12.003. Epub 2009 Dec 16.
We assessed morphology and ERalpha protein and gene expression of two breast cancer cell lines after three different fixatives: neutral-buffered 10% formaldehyde, LN-FIX and FineFIX and varying fixation times. We found that the cell morphology was best preserved in cells fixed with LN-FIX. Two commercial fixatives used in this study shrank cells less than formalin. In immunohistochemical assay samples were stained with two different ERalpha antibodies, clone 1D5 and clone SP1. All tested fixatives were suitable for immunohistochemistry. Staining was more intensive and the number of stained cells was larger with the clone 1D5 than with the clone SP1. Our gene expression analysis showed that formalin and LN-FIX preserve the ERalpha better than FineFIX, which is advertised to be optimal for molecular analysis. Our study suggests that tissues fixed with formalin are suitable also for molecular biology assays. This makes possible to research formalin-fixed paraffin-embedded archival tissues also with molecular techniques.
中性缓冲 10%甲醛、LN-FIX 和 FineFIX 以及不同固定时间后的形态和 ERalpha 蛋白和基因表达。我们发现 LN-FIX 固定的细胞形态保存最好。本研究中使用的两种商业固定剂比福尔马林收缩细胞的程度小。在免疫组织化学检测中,样品用两种不同的 ERalpha 抗体,克隆 1D5 和克隆 SP1 染色。所有测试的固定剂都适合免疫组织化学。与克隆 SP1 相比,克隆 1D5 的染色更强烈,染色细胞数量更多。我们的基因表达分析表明,福尔马林和 LN-FIX 比 FineFIX 更能保存 ERalpha,后者被宣传为最适合分子分析。我们的研究表明,福尔马林固定的组织也适用于分子生物学检测。这使得使用分子技术研究福尔马林固定石蜡包埋的存档组织成为可能。