Gandhi Puneet, Khare Richa
Department of Research, Bhopal Memorial Hospital & Research Centre, BHOPAL-38, INDIA.
Turk Patoloji Derg. 2018;34(1):57-65. doi: 10.5146/tjpath.2017.01405.
Autofluorescence induced interference is one of the major drawbacks in immunofluorescence analysis of formalin-fixed paraffin-embedded tissues, as it decreases the signal-to-noise ratio of specific labeling. Apart from aldehyde-fixation induced artifacts; collagen and elastin, red blood cells and endogenous fluorescent pigment lipofuscin are prime sources of autofluorescence in vascular and aging tissues. We describe herein, an optimized indirect-immunofluorescence method for archival formalin-fixed paraffin-embedded tissues tissues and cryo sections, using a combination of 3-reagents in a specific order, to achieve optimal fluorescence signals and imaging.
Human telomerase reverse transcriptase, a protein implicated as a proliferation marker, was chosen relevant to its expression in solid tumors along with 3 other intracellular proteins exhibiting nuclear and/or cytoplasmic expression. Staining was performed on 10 glioma tissue sections along with 5 of their cryo sections, 5 sections each of hepatocellular, lung, papillary-thyroid and renal cell carcinoma, with 10 non-malignant brain tissue samples serving as control. Specimens were imaged using epifluorescence microscopy, followed by software-based quantification of fluorescence signals for statistical analysis and validation.
We observed that the combined application of sodium-borohydride followed by crystal violet before antigen retrieval and a Sudan black B treatment after secondary antibody application proved to be most efficacious for masking autofluorescence/non-specific background in vascular tissues.
This unique trio-methodology provides quantifiable observations with maximized fluorescence signal intensity of the target protein for longer retention time of the signal even after prolonged storage. The results can be extrapolated to other human tissues for different protein targets.
自体荧光诱导干扰是福尔马林固定石蜡包埋组织免疫荧光分析的主要缺点之一,因为它会降低特异性标记的信噪比。除了醛固定诱导的伪像外,胶原蛋白、弹性蛋白、红细胞和内源性荧光色素脂褐素是血管和衰老组织中自体荧光的主要来源。我们在此描述一种针对存档福尔马林固定石蜡包埋组织和冷冻切片的优化间接免疫荧光方法,使用三种试剂按特定顺序组合,以实现最佳荧光信号和成像。
选择人端粒酶逆转录酶(一种被认为是增殖标志物的蛋白质),因其在实体瘤中的表达以及其他三种表现出核和/或细胞质表达的细胞内蛋白质。对10个胶质瘤组织切片及其5个冷冻切片、肝细胞癌、肺癌、乳头状甲状腺癌和肾细胞癌各5个切片进行染色,以10个非恶性脑组织样本作为对照。使用落射荧光显微镜对标本进行成像,然后基于软件对荧光信号进行定量分析,以进行统计分析和验证。
我们观察到,在抗原修复前依次应用硼氢化钠和结晶紫,以及在二抗应用后进行苏丹黑B处理,对于掩盖血管组织中的自体荧光/非特异性背景最为有效。
这种独特的三联方法可提供可量化的观察结果,使目标蛋白的荧光信号强度最大化,即使在长期储存后信号保留时间也更长。该结果可外推至针对不同蛋白质靶点的其他人体组织。