Shenzhen University Health Science Center, Shenzhen, Guangdong, China.
Institute of Urology and Department of Urology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Biomed Res Int. 2020 Mar 19;2020:1497175. doi: 10.1155/2020/1497175. eCollection 2020.
Atopic dermatitis (AD) is a chronic inflammatory skin disease which is often associated with () colonization. ingredients are potential ligands to activate the Toll-like receptor 2 (TLR2) and drive inflammatory cytokine or chemokine production. However, the role of TLR2-mediated chemokine expression in AD development has not been systematically investigated. In this study, we sought to determine the mode of TLR2-mediated chemokine expression in AD patients. Human peripheral blood mononuclear cells (PBMCs) were isolated from AD patients and healthy controls. Upon incubation with TLR2 ligands Pam3CSK4 and PGN, mRNA expression of chemokines, including CCL1, CCL5, CCL8, CCL13, CCL17, CCL18, CCL22, and CCL27, were determined by quantitative real-time polymerase chain reaction (qRT-PCR) analysis. The results showed that basal mRNA expression of CCL17 in PBMCs from AD patients was upregulated compared with healthy controls, while those of CCL8 and CCL13 were downregulated. When stimulated with TLR2 ligands, the mRNA expression of CCL5, CCL8, CCL13, CCL18, and CCL22 in PBMCs from AD patients was significantly higher than those from healthy controls. The different basal chemokine mRNA expression profiles indicate the different immune status in patients with AD compared with healthy controls. Excessive chemokine mRNA expression induced by TLR2 activation is associated with the development of AD.
特应性皮炎(AD)是一种慢性炎症性皮肤病,常伴有 ( )定植。成分是潜在的配体,可以激活 Toll 样受体 2(TLR2)并驱动炎症细胞因子或趋化因子的产生。然而,TLR2 介导的趋化因子表达在 AD 发展中的作用尚未得到系统研究。在本研究中,我们试图确定 TLR2 介导的趋化因子在 AD 患者中的表达模式。从 AD 患者和健康对照者中分离外周血单核细胞(PBMC)。用 TLR2 配体 Pam3CSK4 和 PGN 孵育后,通过定量实时聚合酶链反应(qRT-PCR)分析测定趋化因子(包括 CCL1、CCL5、CCL8、CCL13、CCL17、CCL18、CCL22 和 CCL27)的 mRNA 表达。结果表明,与健康对照组相比,AD 患者 PBMC 中 CCL17 的基础 mRNA 表达上调,而 CCL8 和 CCL13 的基础 mRNA 表达下调。当用 TLR2 配体刺激时,AD 患者 PBMC 中 CCL5、CCL8、CCL13、CCL18 和 CCL22 的 mRNA 表达明显高于健康对照组。不同的基础趋化因子 mRNA 表达谱表明 AD 患者与健康对照组的免疫状态不同。TLR2 激活诱导的过度趋化因子 mRNA 表达与 AD 的发生有关。