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金黄色葡萄球菌丝氨酸蛋白酶样蛋白 A(SplA)可诱导角质形成细胞产生白细胞介素-8(IL-8),并与白细胞介素-17A 协同作用。

Staphylococcus aureus Serine protease-like protein A (SplA) induces IL-8 by keratinocytes and synergizes with IL-17A.

机构信息

Translational Immunology in Environmental Medicine, School of Medicine and Health, Technical University of Munich, Munich, Germany; Vascular Surgery, Faculty of Medicine, University of Augsburg, Augsburg, Germany.

Translational Immunology in Environmental Medicine, School of Medicine and Health, Technical University of Munich, Munich, Germany; Institute of Environmental Medicine, Helmholtz Munich, German Research Center for Environmental Health, Neuherberg, Germany; Translational Immunology, Faculty of Medicine, University of Augsburg, Germany.

出版信息

Cytokine. 2024 Aug;180:156634. doi: 10.1016/j.cyto.2024.156634. Epub 2024 May 28.

Abstract

BACKGROUND

Serine protease-like (Spl) proteins produced by Staphylococcus (S.) aureus have been associated with allergic inflammation. However, effects of Spls on the epidermal immune response have not been investigated.

OBJECTIVES

To assess the epidermal immune response to SplA, SplD and SplE dependent on differentiation of keratinocytes and a Th2 or Th17 cytokine milieu.

METHODS

Human keratinocytes of healthy controls and a STAT3-hyper-IgE syndrome (STAT3-HIES) patient were cultured in different calcium concentrations in the presence of Spls and Th2 or Th17 cytokines. Keratinocyte-specific IL-8 production and concomitant migration of neutrophils were assessed.

RESULTS

SplE and more significantly SplA, induced IL-8 in keratinocytes. Suprabasal-like keratinocytes showed a higher Spl-mediated IL-8 production and neutrophil migration compared to basal-like keratinocytes. Th17 cytokines amplified Spl-mediated IL-8 production, which correlated with neutrophil recruitment. Neutrophil recruitment by keratinocytes of the STAT3-HIES patient was similar to healthy control cells.

CONCLUSION

S. aureus-specific Spl proteases synergized with IL-17A on human keratinocytes with respect to IL-8 release and neutrophil migration, highlighting the importance of keratinocytes and Th17 immunity in barrier function.

摘要

背景

金黄色葡萄球菌(S. aureus)产生的丝氨酸蛋白酶样(Spl)蛋白与过敏炎症有关。然而,Spl 对表皮免疫反应的影响尚未得到研究。

目的

评估依赖于角质形成细胞分化和 Th2 或 Th17 细胞因子环境的 SplA、SplD 和 SplE 对表皮免疫反应的影响。

方法

在存在 Spl 和 Th2 或 Th17 细胞因子的情况下,培养来自健康对照者和 STAT3 高免疫球蛋白 E 综合征(STAT3-HIES)患者的角质形成细胞,在不同的钙离子浓度下进行培养。评估角质形成细胞特异性白细胞介素-8(IL-8)的产生和伴随的中性粒细胞迁移。

结果

SplE 以及更显著的 SplA 可诱导角质形成细胞产生 IL-8。与基底样角质形成细胞相比,超基底层样角质形成细胞显示出更高的 Spl 介导的 IL-8 产生和中性粒细胞迁移。Th17 细胞因子增强了 Spl 介导的 IL-8 产生,与中性粒细胞募集相关。STAT3-HIES 患者的角质形成细胞的中性粒细胞募集与健康对照细胞相似。

结论

金黄色葡萄球菌特异性 Spl 蛋白酶与 IL-17A 协同作用于人类角质形成细胞,促进白细胞介素-8 的释放和中性粒细胞的迁移,突出了角质形成细胞和 Th17 免疫在屏障功能中的重要性。

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