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用两种抗角蛋白单克隆抗体对正常人表皮细胞中的角蛋白丝进行免疫金标记。

Immunogold labeling of keratin filaments in normal human epidermal cells with two anti-keratin monoclonal antibodies.

作者信息

Haftek M, Staquet M J, Viac J, Schmitt D, Thivolet J

出版信息

J Histochem Cytochem. 1986 May;34(5):613-8. doi: 10.1177/34.5.2422248.

Abstract

We report on application of the highly sensitive and specific immunogold labeling method for ultrastructural investigation of keratin intermediate filament antigens in human epidermal cell suspensions. Triton X-100 pretreated cells proved accessible to the colloidal gold conjugate, thus enabling keratin filament bundles to be labeled. Anti-keratin KL1 and KL2 monoclonal antibodies were raised in mice after immunization with either human stratum corneum-isolated keratins or keratins extracted from human epidermal cells suspensions, respectively. Immunoelectron microscopy confirmed immunofluorescence and immunoperoxidase results of epidermal keratinocyte staining, and revealed two different antibody reactivity patterns: KL2 reacted with keratin filaments in keratinocytes of all epidermal layers, whereas antigen to KL1 was detected only on keratin of the suprabasal layers, not on the basal keratinocyte tonofilaments. The monoclonal antibody-recognized epitopes were specific for the keratin filaments. Vimentin-rich cells (melanocytes) were not stained in the same epidermal cell suspensions. Additionally, two distinct ultrastructural patterns of keratin filament epitope labeling were observed. KL1 and KL2 monoclonal antibodies react with two different antigenic determinants, depending on the stage of keratinocyte differentiation, and may therefore be used for immunohistochemical studies of various keratin-containing cells in normal and pathologic conditions.

摘要

我们报告了高灵敏度和特异性免疫金标记方法在人表皮细胞悬液中角蛋白中间丝抗原超微结构研究中的应用。经Triton X - 100预处理的细胞可被胶体金缀合物标记,从而能够标记角蛋白丝束。分别用人角质层分离的角蛋白或从人表皮细胞悬液中提取的角蛋白免疫小鼠后,制备了抗角蛋白KL1和KL2单克隆抗体。免疫电子显微镜证实了表皮角质形成细胞染色的免疫荧光和免疫过氧化物酶结果,并揭示了两种不同的抗体反应模式:KL2与所有表皮层角质形成细胞中的角蛋白丝反应,而KL1的抗原仅在上基底层的角蛋白上检测到,在基底角质形成细胞张力丝上未检测到。单克隆抗体识别的表位对角蛋白丝具有特异性。富含波形蛋白的细胞(黑素细胞)在相同的表皮细胞悬液中未被染色。此外,观察到角蛋白丝表位标记的两种不同超微结构模式。KL1和KL2单克隆抗体根据角质形成细胞分化阶段与两种不同的抗原决定簇反应,因此可用于正常和病理条件下各种含角蛋白细胞的免疫组织化学研究。

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