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免疫电子显微镜技术在基底膜抗原研究中的评估

Evaluation of immunoelectron microscopic techniques in the study of basement membrane antigens.

作者信息

Masunaga T, Shimizu H, Ishiko A, Nishikawa T

机构信息

Department of Dermatology, Keio University School of Medicine, Tokyo, Japan.

出版信息

Histochem Cell Biol. 1998 Aug;110(2):107-11. doi: 10.1007/s004180050271.

Abstract

Recent technical advances in immunoelectron microscopy (IEM), including methods of pre- and postembedding IEM and cryoultramicrotomy, have helped to elucidate the precise ultrastructural localization of various basement membrane-related molecules. Our objective was to evaluate the advantages and disadvantages of several different techniques for studying the ultrastructural organization of basement membrane components. We found that, while "on-surface" immunolabeling of postembedding IEM and cryoultramicrotomy with anti-type IV collagen or anti-laminin-5 antibody clearly demonstrated dense labeling on the lamina densa, preembedding IEM with a 1-nm ultra-small gold probe showed labeling only on the epidermal and/or dermal surfaces of the lamina densa, with no specific gold particles being seen within the lamina densa itself. These results indicate that even ultra-small colloidal gold-labeled antibody fails to penetrate the lamina densa in preembedding IEM. However, labeling with a GB3 monoclonal antibody against laminin-5 was demonstrable with preembedding IEM and cryoultramicrotomy, but not with postembedding IEM, probably due to a loss of antigenicity. These results confirm the advantages and limitations of these techniques of IEM and emphasize the importance of using different techniques of IEM in determining the precise ultrastructural distribution of basement membrane antigens.

摘要

免疫电子显微镜(IEM)的最新技术进展,包括包埋前和包埋后IEM以及冷冻超薄切片技术,有助于阐明各种基底膜相关分子的精确超微结构定位。我们的目的是评估几种不同技术在研究基底膜成分超微结构组织方面的优缺点。我们发现,虽然用抗IV型胶原或抗层粘连蛋白-5抗体对包埋后IEM和冷冻超薄切片进行“表面”免疫标记清楚地显示了致密板上的密集标记,但用1纳米超小金探针进行包埋前IEM仅在致密板的表皮和/或真皮表面显示标记,在致密板本身内未见特异性金颗粒。这些结果表明,即使是超小胶体金标记抗体在包埋前IEM中也无法穿透致密板。然而,用抗层粘连蛋白-5的GB3单克隆抗体进行标记在包埋前IEM和冷冻超薄切片中是可行的,但在包埋后IEM中不可行,这可能是由于抗原性丧失所致。这些结果证实了这些IEM技术的优点和局限性,并强调了在确定基底膜抗原的精确超微结构分布时使用不同IEM技术的重要性。

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