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Multilabel immunofluorescence and antigen reprobing on formalin-fixed paraffin-embedded sections: novel applications for precision pathology diagnosis

机译:福尔马林固定石蜡包埋的切片上的多标记免疫荧光和抗原探测:精确病理诊断的新应用

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We report new methods for multilabel immunofluorescence (MIF) and reprobing of antigen epitopes on the same formalin-fixed paraffin-embedded (FFPE) sections. The MIF method includes an antigen-retrieval step followed by multilabel immunostaining and examination by confocal microscopy. As examples, we illustrate epitopes localized to the apical and basolateral membranes, and the cytoplasm of enterocytes of normal small intestine and in cases of congenital enteropathies (microvillous inclusion disease and congenital tufting enteropathy). We also demonstrate localization of the bile salt excretion pump protein (BSEP) in bile canalicular membrane of normal hepatocytes and in cases of primary sclerosing cholangitis. To demonstrate colocalization of cytoplasmic and nuclear epitopes we analyzed normal control and hyperplastic pulmonary neuroendocrine cells (PNEC) and neuroepithelial bodies (NEBs), presumed airway sensors in the lungs of infants with bronchopulmonary dysplasia (BPD). As cytoplasmic markers we used anti-bombesin or anti-synaptic vesicle protein 2 (SV2) antibody, respectively, and for nuclear localization, antibodies against neurogenic genes mammalian achaete-scute homolog (Mash1) and prospero homeobox 1 (Prox1), essential for NEB cells differentiation and maturation, hypoxia-inducible factor 1伪 (HIF1伪) a downstream modulator of hypoxia response and a proliferation marker Ki67. The reprobing method consisted of removal of the previously immunolabeled target and immunostaining with different antibodies, facilitating colocalization of enterocyte brush border epitopes as well as HIF1伪, Mash1 and Prox1 in PNEC/NEB PNEC and NEBs. As these methods are suitable for routine FFPE pathology samples from various tissues, allowing visualization of multiple epitopes in the same cells/sections with superior contrast and resolution, they are suitable for a wide range of applications in diagnostic pathology and may be particularly well suited for precision medicine diagnostics.
机译:我们报告了多标签免疫荧光(MIF)和相同的福尔马林固定石蜡包埋(FFPE)部分上抗原表位的探测新方法。 MIF方法包括抗原回收步骤,然后进行多标记免疫染色和共聚焦显微镜检查。例如,我们说明了位于正常小肠和先天性肠病(微毛包涵体疾病和先天簇状肠病)病例中位于表皮和顶外侧膜的表位以及肠上皮细胞的胞质。我们还证明了胆汁盐排泄泵蛋白(BSEP)在正常肝细胞的胆管膜和原发性硬化性胆管炎的情况下的定位。为了证明胞质和核表位的共定位,我们分析了正常对照和增生性肺神经内分泌细胞(PNEC)和神经上皮体(NEB),以及支气管肺发育不良(BPD)婴儿肺中的气道传感器。作为细胞质标记,我们分别使用了抗bombesin或抗突触小泡蛋白2(SV2)抗体,而对于核定位,则使用了针对神经源性基因例如哺乳动物achaete-scute同源物(Mash1)和prospero同源盒1(Prox1)的抗体,这对于NEB是必不可少的细胞分化和成熟,缺氧诱导因子1α(HIF1α),缺氧反应的下游调节剂和增殖标记Ki67。重新探测方法包括去除先前免疫标记的靶标并用不同的抗体进行免疫染色,以促进肠上皮细胞刷状边界表位以及HIF1α,Mash1和Prox1在PNEC / NEB PNEC和NEB中的共定位。由于这些方法适用于来自各种组织的常规FFPE病理学样品,可在同一细胞/切片中以优异的对比度和分辨率可视化多个表位,因此它们适用于诊断病理学的广泛应用,并且可能特别适合于精密医学诊断。

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