Ramos-Vara J A, Webster J D, DuSold D, Miller M A
Animal Disease Diagnostic Laboratory and Department of Comparative Pathobiology, Purdue University, 406 South University, West Lafayette, IN 47907, USA. Email:
Vet Pathol. 2014 Jan;51(1):102-9. doi: 10.1177/0300985813476067. Epub 2013 Feb 22.
Environmental stresses can alter immunoreactivity of biomarkers in stored tissue sections. The effect of temperature and lighting on 49 cellular or microbial antigens was evaluated in 4 serial paraffin sections, cut 12 months, 10 months, 8 months, 5 months, 3 months, 1 month, 3 days, and 1 day before immunohistochemistry. Slides were stored at room temperature (RT) in the dark, at 4°C in the dark, at RT under fluorescent light, or at RT with windowpane exposure to sunlight. Immunohistochemistry was performed simultaneously in an automated immunostainer. Immunoreactivity was compared with that in the corresponding 1-day-old section and scored as 4 (<10% reduction), 3 (10%-25% reduction), 2 (26%-60% reduction), 1(>60% reduction), or 0 (no reactivity). Any loss of immunoreactivity was proportional to the tissue section age and was least in sections stored in the dark. Immunoreactivity was only completely lost in light-exposed sections and as early as 1 month for CD45. Other markers with complete loss of immunoreactivity were bovine viral diarrhea virus, CD18 (only with fluorescent light), CD31, CD68, canine parvovirus, chromogranins, and thyroid transcription factor-1. Markers with complete loss after light exposure also had reduced immunoreactivity when stored in the dark, as early as day 3. Eight markers (Bartonella spp, CD11d, high molecular weight cytokeratins, feline coronavirus, GATA-4, insulin, p63, progesterone receptor) had minimal decrease in immunoreactivity, regardless of treatment. In conclusion, light-induced antigen decay (tissue section aging) is antigen dependent and could explain unexpectedly weak or negative immunohistochemical reactions in stored paraffin sections.
环境应激可改变储存组织切片中生物标志物的免疫反应性。在免疫组织化学前12个月、10个月、8个月、5个月、3个月、1个月、3天和1天分别切取4个连续石蜡切片,评估温度和光照对49种细胞或微生物抗原的影响。玻片分别在室温(RT)黑暗条件下、4℃黑暗条件下、室温荧光灯下或室温有窗户直射阳光条件下储存。在自动免疫染色仪中同时进行免疫组织化学。将免疫反应性与相应的1日龄切片进行比较,并评分为4(减少<10%)、3(减少10%-25%)、2(减少26%-60%)、1(减少>60%)或0(无反应性)。免疫反应性的任何丧失都与组织切片的年龄成正比,且在黑暗中储存的切片中最少。免疫反应性仅在暴露于光的切片中完全丧失,对于CD45最早在1个月时就完全丧失。其他免疫反应性完全丧失的标志物有牛病毒性腹泻病毒、CD18(仅在荧光灯下)、CD31、CD68、犬细小病毒、嗜铬粒蛋白和甲状腺转录因子-1。暴露于光后完全丧失免疫反应性的标志物在黑暗中储存时,早在第3天免疫反应性也会降低。8种标志物(巴尔通体属、CD11d、高分子量细胞角蛋白、猫冠状病毒、GATA-4、胰岛素、p63、孕激素受体)无论处理如何,免疫反应性降低都最小。总之,光诱导的抗原衰变(组织切片老化)是抗原依赖性的,这可以解释储存石蜡切片中意外出现的弱或阴性免疫组化反应。