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结节病中功能性Toll样受体9表达及CXCR3配体释放

Functional Toll-Like Receptor 9 Expression and CXCR3 Ligand Release in Pulmonary Sarcoidosis.

作者信息

Schnerch Jasmin, Prasse Antje, Vlachakis Dimitrios, Schuchardt Kathrin L, Pechkovsky Dmitri V, Goldmann Torsten, Gaede Karoline I, Müller-Quernheim Joachim, Zissel Gernot

机构信息

1 Department of Pneumology, Centre for Medicine, Medical Centre-University of Freiburg, Freiburg, Germany.

2 Respiratory Division, Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.

出版信息

Am J Respir Cell Mol Biol. 2016 Nov;55(5):749-757. doi: 10.1165/rcmb.2015-0278OC.

Abstract

Sarcoidosis is a granulomatous disease characterized by a T-helper type 1 (Th1) cell-dominated alveolitis. As a role of bacteria in the pathogenesis of sarcoidosis has been discussed, Toll-like receptors (TLRs) may be involved in the initiation of a first immune reaction. We analyzed expression and functional relevance of several TLRs in bronchoalveolar lavage (BAL) cells from patients with pulmonary sarcoidosis. In parallel, we determined the release of C-X-C motif chemokine 9 (CXCL9), CXCL10, and CXCL11 by BAL cells from patients with pulmonary sarcoidosis. Nucleotide-binding oligomerization domain-containing protein (NOD) 1 and 2, TLR2, TLR6, and TLR9 expression by BAL cells was analyzed by real-time RT-PCR and cell surface expression by flow cytometry. Chemokine release was measured in BAL cell culture supernatants by ELISA. We found increased TLR9 mRNA expression in patients with sarcoidosis with chest X-ray type I and II and TLR9 protein expression in BAL cells from patients with chest X-ray type II and III. Stimulation with CpG nucleotides increased CXCL10 release by BAL cells from patients with sarcoidosis type II significantly compared with control subjects or other patients with sarcoidosis. In contrast, no increase in TNF, IL-12p40, or CXCL8 was detected. Spontaneous release of CXCL10, but not CXCL9 or CXCL11, by cultured BAL cells was also highest in cells from patients with chest X-ray type II. We found a significant association between TLR9 expression and CD4 lymphocytes in BAL. Our data demonstrate that TLR9 ligands may contribute to the immunopathogenesis of sarcoidosis via induction of CXCL10 release in the alveolar macrophages.

摘要

结节病是一种以1型辅助性T(Th1)细胞为主导的肺泡炎为特征的肉芽肿性疾病。由于细菌在结节病发病机制中的作用已被讨论,Toll样受体(TLR)可能参与首次免疫反应的启动。我们分析了肺结节病患者支气管肺泡灌洗(BAL)细胞中几种TLR的表达及其功能相关性。同时,我们测定了肺结节病患者BAL细胞中C-X-C基序趋化因子9(CXCL9)、CXCL10和CXCL11的释放。通过实时逆转录聚合酶链反应(RT-PCR)分析BAL细胞中含核苷酸结合寡聚化结构域蛋白(NOD)1和2、TLR2、TLR6和TLR9的表达,并通过流式细胞术分析细胞表面表达。通过酶联免疫吸附测定(ELISA)法检测BAL细胞培养上清液中的趋化因子释放。我们发现,胸部X线表现为I型和II型的结节病患者TLR9信使核糖核酸(mRNA)表达增加,胸部X线表现为II型和III型的患者BAL细胞中TLR9蛋白表达增加。与对照组或其他结节病患者相比,用CpG核苷酸刺激后,II型结节病患者BAL细胞中CXCL10的释放显著增加。相反,未检测到肿瘤坏死因子(TNF)、白细胞介素-12p40或CXCL8增加。培养的BAL细胞自发释放CXCL10(而非CXCL9或CXCL11)在胸部X线表现为II型的患者细胞中也最高。我们发现BAL中TLR9表达与CD4淋巴细胞之间存在显著关联。我们的数据表明,TLR9配体可能通过诱导肺泡巨噬细胞释放CXCL10而促进结节病的免疫发病机制。

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