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首页> 外文期刊>Veterinary Pathology >Immunohistochemical evaluation of the effects of paraffin section storage on biomarker stability. (Special Focus: Investigative techniques.)
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Immunohistochemical evaluation of the effects of paraffin section storage on biomarker stability. (Special Focus: Investigative techniques.)

机译:免疫组织化学评估石蜡切片储存对生物标志物稳定性的影响。 (特别关注:调查技术。)

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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 degrees 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.
机译:环境压力可能会改变存储的组织切片中生物标志物的免疫反应性。在连续4个连续石蜡切片中分别评估温度和光照对49种细胞或微生物抗原的影响,分别在免疫组织化学前12个月,10个月,8个月,5个月,3个月,1个月,3天和1天进行切割。将载玻片在室温(RT)下在黑暗中,在4摄氏度下在黑暗中,在荧光灯下的RT下或在窗玻璃暴露于阳光下的RT下保存。免疫组织化学在自动免疫染色仪中同时进行。将免疫反应性与相应的1天大的切片进行比较,分别为4分(降低<10%),3分(降低10%-25%),2分(降低26%-60%),1分(> 60%)还原)或0(无反应性)。免疫反应性的任何丧失与组织切片的年龄成正比,并且在黑暗中保存的切片中最少。免疫反应仅在曝光的切片中完全消失,而CD45最早在1个月时消失。免疫反应性完全丧失的其他标记是牛病毒性腹泻病毒,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。暴露在光下完全丧失的标记物,最早在第3天在黑暗中保存时,也会降低免疫反应性。八个标记物(Bartonella spp,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)无论采用何种治疗方法,免疫反应性的降低均很小。总之,光诱导的抗原衰变(组织切片老化)是抗原依赖性的,并且可以解释在储存的石蜡切片中出乎意料的弱或阴性的免疫组织化学反应。

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