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组氨酸增加 Th2 细胞因子诱导的人 M2 巨噬细胞中 CCL18 的表达。

Histamine Increases Th2 Cytokine-Induced CCL18 Expression in Human M2 Macrophages.

机构信息

Division of Immunodermatology and Allergy Research, Department of Dermatology and Allergy, Hannover Medical School, 30625 Hannover, Germany.

Department of Dermatology, Mühlenkreiskliniken AöR, Ruhr University Bochum Campus Minden, 32427 Minden, Germany.

出版信息

Int J Mol Sci. 2021 Oct 28;22(21):11648. doi: 10.3390/ijms222111648.

Abstract

The chemokine CCL18 is produced in cells of the myelomonocytic lineage and represents one of the most highly expressed chemokines in lesional skin and serum of atopic dermatitis patients. We investigated the role of histamine in CCL18 production in human monocyte-derived M2 macrophages differentiated in the presence of M-CSF and activated with IL-4, IL-13 or with IL-10. Since expression and regulation of histamine H1 receptor (H1R), H2R and H4R by IL-4 and IL-13 on human M2 macrophages were described, we analyzed expression of the histamine receptors in response to IL-10 stimulation by quantitative RT-PCR. IL-10 upregulated H2R and downregulated H4R mRNA expression by trend in M2 macrophages. IL-10, but in a more pronounced manner, IL-4 and IL-13, also upregulated CCL18. Histamine increased the cytokine-induced upregulation of CCL18 mRNA expression by stimulating the H2R. This effect was stronger in IL-10-stimulated M2 macrophages where the upregulation of CCL18 was confirmed at the protein level by ELISA using selective histamine receptor agonist and antagonists. The histamine-induced CCL18 upregulation in IL-10-activated M2 macrophages was almost similar in cells obtained from atopic dermatitis patients compared to cells from healthy control persons. In summary, our data stress a new function of histamine showing upregulation of the Th2 cells attracting chemokine CCL18 in human, activated M2 macrophages. This may have an impact on the course of atopic dermatitis and for the development of new therapeutic interventions.

摘要

趋化因子 CCL18 由髓系单核细胞系产生,是特应性皮炎患者皮损皮肤和血清中表达水平最高的趋化因子之一。我们研究了组胺在人单核细胞衍生的 M2 巨噬细胞中的作用,这些巨噬细胞在 M-CSF 存在的情况下分化,并通过 IL-4、IL-13 或 IL-10 激活。由于 IL-4 和 IL-13 对人 M2 巨噬细胞中组胺 H1 受体 (H1R)、H2R 和 H4R 的表达和调节已有描述,我们通过定量 RT-PCR 分析了组胺受体对 IL-10 刺激的表达。IL-10 以趋势上调 M2 巨噬细胞中 H2R 和下调 H4R mRNA 表达。IL-10、更明显的是 IL-4 和 IL-13,也上调了 CCL18。组胺通过刺激 H2R 增加细胞因子诱导的 CCL18 mRNA 表达的上调。在 IL-10 刺激的 M2 巨噬细胞中,这种效应更强,ELISA 用选择性组胺受体激动剂和拮抗剂证实了 CCL18 在蛋白水平的上调。与来自健康对照者的细胞相比,来自特应性皮炎患者的细胞中,IL-10 激活的 M2 巨噬细胞中组胺诱导的 CCL18 上调几乎相似。总之,我们的数据强调了组胺的新功能,即上调人类 Th2 细胞吸引趋化因子 CCL18 的作用,这可能对特应性皮炎的病程和新的治疗干预措施的发展产生影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38cc/8584115/fe45cbd19d1a/ijms-22-11648-g001.jpg

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