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角质形成细胞间黏附连接:人表皮中与桥粒不同的细胞间连接结构的免疫细胞化学可视化。

Interkeratinocyte adherens junctions: immunocytochemical visualization of cell-cell junctional structures, distinct from desmosomes, in human epidermis.

作者信息

Haftek M, Hansen M U, Kaiser H W, Kreysel H W, Schmitt D

机构信息

Department of Dermatology, INSERM, Edouard Herriot Hospital, Lyon, France.

出版信息

J Invest Dermatol. 1996 Mar;106(3):498-504. doi: 10.1111/1523-1747.ep12343791.

Abstract

Vinculin and beta-catenin are intracellular attachment proteins linking transmembrane adhesion molecules (E-cadherin) to the actin microfilament cytoskeleton, thus participating in formation of cell-cell adherens junctions, or zonulae adherentes. This type of junction was only recently described in human epidermis due to the imprecise morphological criteria for its recognition. In this study, we investigated the relationship between the expression of the zonula adherens-associated proteins vinculin, beta-catenin, E-cadherin, and actin, on the one hand, and the presence of electron microscopically discernable structures in normal human epidermis on the other. Mouse jejunal epithelium with its orderly arrangement of various junctional structures served as a positive control. Simple and dual post-embedding immunogold labeling was performed on ultrathin sections of Lowicryl K4M and Lowicryl K11M embedded tissues. The overall distribution of the antigens in human epidermis was evaluated on frozen tissue sections using immunofluorescence and laser confocal scanning microscopy. Antibodies against proteins associated with desmosomes (i.e., keratins, desmoglein 1, and plakoglobin) were used as controls. Vinculin and beta-catenin were localized to junctional structures distinct from desmosomes, thus defining the presence of zonulae adherentes. Labeling of actin and E-cadherin was less clearly restricted to the junctions, but these two proteins were also co-expressed at zonulae adherentes and not at desmosomes. In human epidermis, zonula adherens-associated labeling was consistently detected near desmosomes, indicating the possibility of a functional relationship between the two types of junctions.

摘要

纽蛋白和β-连环蛋白是细胞内附着蛋白,它们将跨膜黏附分子(E-钙黏蛋白)与肌动蛋白微丝细胞骨架相连,从而参与细胞间黏附连接或黏着小带的形成。由于识别这种连接的形态学标准不精确,这种连接类型直到最近才在人类表皮中被描述。在本研究中,我们一方面研究了黏着小带相关蛋白纽蛋白、β-连环蛋白、E-钙黏蛋白和肌动蛋白的表达之间的关系,另一方面研究了正常人类表皮中电子显微镜可分辨结构的存在情况。具有各种连接结构有序排列的小鼠空肠上皮作为阳性对照。对用Lowicryl K4M和Lowicryl K11M包埋的组织超薄切片进行简单和双重包埋后免疫金标记。使用免疫荧光和激光共聚焦扫描显微镜在冷冻组织切片上评估抗原在人类表皮中的总体分布。针对与桥粒相关的蛋白质(即角蛋白、桥粒芯糖蛋白1和桥粒斑珠蛋白)的抗体用作对照。纽蛋白和β-连环蛋白定位于与桥粒不同的连接结构,从而确定了黏着小带的存在。肌动蛋白和E-钙黏蛋白的标记不太明显地局限于连接处,但这两种蛋白质也在黏着小带共表达,而不在桥粒共表达。在人类表皮中,在桥粒附近始终检测到黏着小带相关标记,表明这两种连接类型之间可能存在功能关系。

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