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用2,4-二硝基氟苯和2,4-二硝基硫氰酸苯涂抹小鼠皮肤后,2,4-二硝基苯基在小鼠表皮中的超微结构定位:一项免疫电子显微镜研究

Ultrastructural localization of 2,4-dinitrophenyl groups in mouse epidermis following skin painting with 2,4-dinitrofluorobenzene and 2,4-dinitrothiocyanatebenzene: an immunoelectron microscopical study.

作者信息

Kolde G, Knop J

机构信息

Department of Dermatology, University Münster, Federal Republic of Germany.

出版信息

J Invest Dermatol. 1988 Mar;90(3):320-4. doi: 10.1111/1523-1747.ep12456186.

Abstract

The ultrastructural localization of 2,4-dinitrophenyl (DNP) groups in mouse epidermis after epicutaneous application of the contact sensitizer 2,4-dinitrofluorobenzene (DNFB) and the tolerogen 2,4-dinitrothiocyanatebenzene (DNTB) was investigated at varying times using immunoelectron microscopy with the protein A - gold technique. After application of DNFB, there was a homogenous cytoplasmic labeling of all epidermal cells. The intracellular localization of the DNP groups was not restricted to cytoplasmic organelles belonging to the endocytotic - lysosomal system. The numerous endocytotic organelles, Birbeck granules, and lysosomes of the Langerhans cells (LCs) typically observed after application of contact sensitizers also did not show an increased number of gold particles. Skin painting with DNTB resulted in a similar distribution and time-course of immunolabeling, but this compound did not induce cellular and the endocytotic activation of LCs as seen after DNFB application. These results demonstrate that contact sensitizers do not require specific cellular uptake and intracellular processing by the endocytotic - lysosomal compartment of the LCs before membrane presentation. However, a cellular and endocytotic activation of the LCs by haptens may be an important mechanism for T effector cell activation.

摘要

采用蛋白A-金技术的免疫电子显微镜,在不同时间研究了接触致敏剂2,4-二硝基氟苯(DNFB)和耐受原2,4-二硝基硫氰酸苯(DNTB)经皮应用后,小鼠表皮中2,4-二硝基苯基(DNP)基团的超微结构定位。应用DNFB后,所有表皮细胞的细胞质均呈现均匀标记。DNP基团的细胞内定位并不局限于属于内吞-溶酶体系统的细胞质细胞器。接触致敏剂应用后通常观察到的朗格汉斯细胞(LCs)的大量内吞细胞器、伯贝克颗粒和溶酶体,也未显示金颗粒数量增加。用DNTB涂抹皮肤导致免疫标记的分布和时间进程相似,但该化合物并未像应用DNFB后那样诱导LCs的细胞和内吞激活。这些结果表明,接触致敏剂在膜呈递之前,不需要LCs的内吞-溶酶体区室进行特异性细胞摄取和细胞内加工。然而,半抗原对LCs的细胞和内吞激活可能是T效应细胞激活的重要机制。

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