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在过敏性接触性皮炎激发过程中,CS-1纤连蛋白的表达先于单核细胞趋化蛋白-1的产生。

Expression of CS-1 fibronectin precedes monocyte chemoattractant protein-1 production during elicitation of allergic contact dermatitis.

作者信息

Martín A P, Gagliardi J, Baena-Cagnani C E, Eberhard Y, Uguccioni M, Gallino N, Mariani A L, Serra H M

机构信息

Inmunología, Departamento de Bioquímica Clínica, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba, Córdoba, Argentina.

出版信息

Clin Exp Allergy. 2003 Aug;33(8):1118-24. doi: 10.1046/j.1365-2222.2003.01712.x.

Abstract

BACKGROUND

Leucocyte migration within inflammatory skin compartments in allergic contact dermatitis (ACD) is the result of a sophisticated multi-step event where multiple molecules are involved.

OBJECTIVE

Since non-antigen-specific mechanisms have been described as an early participant in elicitation of ACD, we investigated the kinetics of the expression of monocyte chemoattractant protein-1 (MCP-1/CCL2) and the type of infiltrating cells. We compared the time course production of MCP-1/CCL2 with connecting segment-1 (CS-1) fibronectin and thymus and activation-regulated chemokine (TARC/ CCL17) expression.

METHODS

Biopsies from 10 individuals challenged in their back with the antigen responsible for their contact dermatitis and an irrelevant antigen were taken at different times and histology, immunohistochemistry for CS-1 fibronectin, TARC/CCL17, CD3, CD68, CXCR3, CCR4 and in situ hybridization for MCP-1/CCL2 were performed.

RESULTS

At positive antigen stimulated sites expression of MCP-1/CCL2 by basal keratinocytes and isolated cells in dermis started at 10 h. CS-1 fibronectin and TARC/CCL17 expression by blood endothelial cells was found at 2 and 10 h, respectively. This was followed by dermal accumulation of mononuclear cells with a significant increase of CD3+ and CD68+cells. At 48 h, approximately 58% of infiltrating cells were CXCR3+, and 35% CCR4+.

CONCLUSIONS

We showed evidence of the fact that CS-1 fibronectin expression precedes the production of MCP-1/CCL2 and TARC/CCL17 in the skin of patients with ACD, suggesting that these molecules participate in the early complex process of migrating mononuclear cells during elicitation of ACD.

摘要

背景

在过敏性接触性皮炎(ACD)中,白细胞在炎症性皮肤区域内的迁移是一个复杂的多步骤过程,涉及多种分子。

目的

由于非抗原特异性机制已被描述为引发ACD的早期参与者,我们研究了单核细胞趋化蛋白-1(MCP-1/CCL2)的表达动力学以及浸润细胞的类型。我们比较了MCP-1/CCL2与连接段-1(CS-1)纤连蛋白以及胸腺和活化调节趋化因子(TARC/CCL17)表达的时间进程。

方法

对10名背部用引起其接触性皮炎的抗原和无关抗原进行激发的个体,在不同时间进行活检,并进行组织学检查、CS-1纤连蛋白、TARC/CCL17、CD3、CD68、CXCR3、CCR4的免疫组织化学检查以及MCP-1/CCL2的原位杂交。

结果

在阳性抗原刺激部位,基底角质形成细胞和真皮中分离细胞的MCP-1/CCL2表达在10小时开始。血液内皮细胞的CS-1纤连蛋白和TARC/CCL17表达分别在2小时和10小时被发现。随后是单核细胞在真皮中的积聚,CD3+和CD68+细胞显著增加。在48小时时,约58%的浸润细胞为CXCR3+,35%为CCR4+。

结论

我们证明了在ACD患者皮肤中,CS-1纤连蛋白的表达先于MCP-1/CCL2和TARC/CCL17的产生,这表明这些分子参与了ACD激发过程中单核细胞迁移的早期复杂过程。

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