热诱导抗原回收:机制及其在组织化学中的应用

Q Medicine
Shuji Yamashita
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引用次数: 166

摘要

自Coons等人引入荧光标记抗体方法以来[含荧光基团抗体的免疫学性质]。[j],许多免疫组织化学方法已经改进,以获得高灵敏度的低背景染色,在光镜和电镜水平。Shi等人在20世纪90年代初报道的热诱导抗原回收(HIAR)对福尔马林固定和石蜡包埋(FFPE)材料的免疫组织化学分析做出了巨大贡献,特别是在病理学领域。尽管抗原回收技术包括酶消化、蛋白质变性剂处理和加热被认为是棘手和神秘的技术,但HIAR的机制已经迅速阐明。加热可以切割交联(亚甲基桥)并在甲醛固定的蛋白质和核酸中添加甲基,并延伸多肽以揭示隐藏在抗原内部或被邻近大分子覆盖的表位。在具有适当pH和离子浓度的缓冲液中,由于多肽可能在疏水引力和静电斥力之间取得平衡,表位在冷却过程中暴露而不会缠绕延伸的多肽。近年来的研究表明,HIAR在光镜和电镜下均适用于FFPE材料、冷冻切片、塑料包埋标本、物理固定组织等多种标本的免疫组化,并且表明HIAR的机制与醛固定和非醛固定材料相同。此外,加热已被证明对流式细胞术、核酸组织化学(荧光素原位杂交(FISH)、原位杂交(ISH)和末端脱氧核苷酸转移酶介导的缺口标记(TUNEL))以及FFPE档案材料和经其他程序处理的标本中的大分子提取和分析有效。本文就HIAR的机制及加热在免疫组织化学及其他组织化学反应中的应用作一综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Heat-induced antigen retrieval: Mechanisms and application to histochemistry

Since the introduction of the fluorescence-labeled antibody method by Coons et al. [Immunological properties of antibody containing a fluorescent group. Proc Soc Exp Biol Med 47, 200–2002], many immunohistochemical methods have been refined to obtain high sensitivity with low background staining at both light and electron microscopic levels. Heat-induced antigen retrieval (HIAR) reported by Shi et al. in the early 1990s has greatly contributed to immunohistochemical analysis for formalin-fixed and paraffin-embedded (FFPE) materials, particularly in the field of pathology. Although antigen retrieval techniques including enzyme digestion, treatment with protein denaturants and heating have been considered tricky and mysterious techniques, the mechanisms of HIAR have been rapidly elucidated. Heating cleaves crosslinks (methylene bridges) and add methylol groups in formaldehyde-fixed proteins and nucleic acids and extends polypeptides to unmask epitopes hidden in the inner portion of antigens or covered by adjacent macromolecules. In buffers having an appropriate pH and ion concentration, epitopes are exposed without entangling the extended polypeptides during cooling process, since polypeptides may strike a balance between hydrophobic attraction force and electrostatic repulsion force.

Recent studies have demonstrated that HIAR is applicable for immunohistochemistry with various kinds of specimens, i.e., FFPE materials, frozen sections, plastic-embedded specimens, and physically fixed tissues at both the light- and electron-microscopic levels, and have suggested that the mechanism of HIAR is common to aldehyde-fixed and aldehyde-unfixed materials. Furthermore, heating has been shown to be effective for flow cytometry, nucleic acid histochemistry (fluorescein in situ hybridization (FISH), in situ hybridization (ISH), and terminal deoxynucleotidyl transferase-mediated nick labeling (TUNEL)), and extraction and analysis of macromolecules in both FFPE archive materials and specimens processed by other procedures. In this article, we review mechanism of HIAR and application of heating in both immunohistochemistry and other histochemical reactions.

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来源期刊
CiteScore
4.67
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Progress in Histochemistry and Cytochemistry publishes comprehensive and analytical reviews within the entire field of histochemistry and cytochemistry. Methodological contributions as well as papers in the fields of applied histo- and cytochemistry (e.g. cell biology, pathology, clinical disciplines) will be accepted.
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