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肾上腺髓质素抑制肿瘤坏死因子α诱导的人牙龈成纤维细胞产生CXC趋化因子配体10。

Adrenomedullin suppresses tumour necrosis factor alpha-induced CXC chemokine ligand 10 production by human gingival fibroblasts.

作者信息

Hosokawa I, Hosokawa Y, Ozaki K, Nakae H, Matsuo T

机构信息

Department of Conservative Dentistry, Institute of Health Biosciences, The University of Tokushima Graduate School, Tokushima, Japan.

出版信息

Clin Exp Immunol. 2008 Jun;152(3):568-75. doi: 10.1111/j.1365-2249.2008.03647.x. Epub 2008 Apr 24.

Abstract

Periodontal disease is an inflammatory disorder characterized by the involvement of chemokines that are important for the recruitment of leucocytes. Several cytokines, including tumour necrosis factor alpha (TNF-alpha), are involved in regulating levels of chemokines in periodontal disease. CXC chemokine ligand 10 (CXCL10) is a chemokine related to the migration of T helper 1 cells. In this study, we examined CXCL10 expression in human gingival fibroblasts (HGFs). Moreover, we investigated the effects of adrenomedullin (AM), which is a multi-functional regulatory peptide, on the production of CXCL10 by HGFs. We revealed that TNF-alpha stimulation induced CXCL10 production by HGFs. HGFs expressed AM and AM receptors, calcitonin-receptor-like receptor (CRLR) and receptor-activity-modifying protein (RAMP) 2, mRNAs constitutively. AM treatment supressed CXCL10 production by TNF-alpha-stimulated HGFs. Moreover, we elucidated that AM produced by HGFs inhibited CXCL10 production by HGFs, because AM antagonist enhanced CXCL10 production by HGFs. TNF-alpha treatment enhanced CRLR and RAMP2 mRNA expression in HGFs. Furthermore, AM is expressed in human periodontal tissues, including both inflamed and clinically healthy tissues. These results suggest that the CXCL10 produced by HGFs may be involved in the migration of leucocytes into inflamed tissues and related to exacerbation of periodontal disease. AM might be a therapeutic target of periodontal disease, because AM can inhibit CXCL10 production by HGFs.

摘要

牙周病是一种炎症性疾病,其特征在于趋化因子的参与,这些趋化因子对于白细胞的募集很重要。包括肿瘤坏死因子α(TNF-α)在内的几种细胞因子参与调节牙周病中趋化因子的水平。CXC趋化因子配体10(CXCL10)是一种与辅助性T1细胞迁移相关的趋化因子。在本研究中,我们检测了人牙龈成纤维细胞(HGFs)中CXCL10的表达。此外,我们研究了多功能调节肽肾上腺髓质素(AM)对HGFs产生CXCL10的影响。我们发现TNF-α刺激可诱导HGFs产生CXCL10。HGFs组成性表达AM及其受体降钙素受体样受体(CRLR)和受体活性修饰蛋白(RAMP)2的mRNA。AM处理可抑制TNF-α刺激的HGFs产生CXCL10。此外,我们阐明HGFs产生的AM可抑制HGFs产生CXCL10,因为AM拮抗剂可增强HGFs产生CXCL10。TNF-α处理可增强HGFs中CRLR和RAMP2 mRNA的表达。此外,AM在包括炎症组织和临床健康组织在内的人牙周组织中表达。这些结果表明,HGFs产生的CXCL10可能参与白细胞向炎症组织的迁移,并与牙周病的加重有关。AM可能是牙周病的治疗靶点,因为AM可抑制HGFs产生CXCL10。

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