{"title":"免疫组化新手指南","authors":"Majda El Hassani, Cristina Cocco","doi":"10.1042/bio_2024_112","DOIUrl":null,"url":null,"abstract":"Using the affinity between antibodies and antigens, immunohistochemistry (IHC) is a helpful method for analysing the cellular components within tissue sections placed on glass slides. The chemistry of antibodies was not discovered until 1941, and since then, their use has increased due to the discovery of enzymes and fluorochromes conjugated to antibodies, enabling observations through optical or fluorescence microscopy (FM). Hence, immunofluorescence (IF), or IHC with fluorescent antibodies, has been associated with the advancement of FM and fluorochromes. Specifically, the discovery of three fluorochromes that emit blue, red and green led to a rise in IF application in the context of visualizing numerous components in a single cell. The proximity ligation assay (PLA) method, so termed because the antibody is conjugated with short DNA strands called PLA probes, is the most recent development in the field of antibody conjugation. Protein–protein interactions and sub-localization of proteins can both be studied using this technique. The improvement of conjugation techniques has occurred in parallel with the development of sophisticated microscopies, including confocal and slide scanners. Confocal microscopy allows for the reconstruction of three-dimensional structures while a slide scanner can digitally convert up to 100 slides' worth of high-resolution pictures. The first step in the IHC process is the collection and fixation of tissues from animal models and humans. Paraformaldehyde is the most commonly used fixative. Fixation prevents antigen blocking and creates cross-links between proteins to preserve tissue structures. Fixation is followed by cutting tissues using microtome or cryostat, then slides are treated for antigen exposition (antigen retrieval) and then included in Triton X solution, which increases membrane permeability. Subsequently, incubations with enzyme- or fluorochrome-conjugated antibodies enable observations via optical microscopy or FM, respectively. In clinical practice and research, IHC and IF are still helpful methods for identifying the antigen-proteins linked to specific diseases.","PeriodicalId":510527,"journal":{"name":"The Biochemist","volume":"186 4","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-05-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A beginner’s guide to immunohistochemistry\",\"authors\":\"Majda El Hassani, Cristina Cocco\",\"doi\":\"10.1042/bio_2024_112\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Using the affinity between antibodies and antigens, immunohistochemistry (IHC) is a helpful method for analysing the cellular components within tissue sections placed on glass slides. 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引用次数: 0
摘要
利用抗体与抗原之间的亲和力,免疫组化(IHC)是分析玻璃片上组织切片中细胞成分的一种有效方法。抗体的化学性质直到 1941 年才被发现,此后,由于酶和与抗体结合的荧光素的发现,抗体的使用越来越多,从而可以通过光学显微镜或荧光显微镜(FM)进行观察。因此,免疫荧光(IF)或使用荧光抗体的 IHC 与荧光显微镜和荧光染料的发展息息相关。具体来说,蓝、红、绿三种荧光染料的发现使免疫荧光技术在单细胞内多种成分的可视化方面得到了广泛应用。近距离连接检测法(PLA)是抗体连接领域的最新发展,因为抗体与称为 PLA 探针的 DNA 短链连接在一起。蛋白质与蛋白质之间的相互作用和蛋白质的亚定位都可以用这种技术来研究。共轭技术的改进是与共聚焦显微镜和载玻片扫描仪等先进显微镜的发展同步进行的。共聚焦显微镜可重建三维结构,而玻片扫描仪可将多达 100 张玻片的高分辨率图片进行数字转换。IHC 过程的第一步是收集和固定动物模型和人体组织。多聚甲醛是最常用的固定剂。固定可防止抗原阻塞,并在蛋白质之间产生交联以保存组织结构。固定后使用显微切片机或低温恒温器切割组织,然后对切片进行抗原暴露处理(抗原回收),再放入 Triton X 溶液中,以增加膜的通透性。随后,用酶或荧光标记抗体进行孵育,分别通过光学显微镜或荧光显微镜进行观察。在临床实践和研究中,IHC 和 IF 仍是鉴别与特定疾病相关的抗原蛋白的有效方法。
Using the affinity between antibodies and antigens, immunohistochemistry (IHC) is a helpful method for analysing the cellular components within tissue sections placed on glass slides. The chemistry of antibodies was not discovered until 1941, and since then, their use has increased due to the discovery of enzymes and fluorochromes conjugated to antibodies, enabling observations through optical or fluorescence microscopy (FM). Hence, immunofluorescence (IF), or IHC with fluorescent antibodies, has been associated with the advancement of FM and fluorochromes. Specifically, the discovery of three fluorochromes that emit blue, red and green led to a rise in IF application in the context of visualizing numerous components in a single cell. The proximity ligation assay (PLA) method, so termed because the antibody is conjugated with short DNA strands called PLA probes, is the most recent development in the field of antibody conjugation. Protein–protein interactions and sub-localization of proteins can both be studied using this technique. The improvement of conjugation techniques has occurred in parallel with the development of sophisticated microscopies, including confocal and slide scanners. Confocal microscopy allows for the reconstruction of three-dimensional structures while a slide scanner can digitally convert up to 100 slides' worth of high-resolution pictures. The first step in the IHC process is the collection and fixation of tissues from animal models and humans. Paraformaldehyde is the most commonly used fixative. Fixation prevents antigen blocking and creates cross-links between proteins to preserve tissue structures. Fixation is followed by cutting tissues using microtome or cryostat, then slides are treated for antigen exposition (antigen retrieval) and then included in Triton X solution, which increases membrane permeability. Subsequently, incubations with enzyme- or fluorochrome-conjugated antibodies enable observations via optical microscopy or FM, respectively. In clinical practice and research, IHC and IF are still helpful methods for identifying the antigen-proteins linked to specific diseases.