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干扰素基因刺激物(STING)的激活与干燥综合征。

Activation of Stimulator of Interferon Genes (STING) and Sjögren Syndrome.

机构信息

1 Arthritis and Clinical Immunology Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.

2 Comparative Medicine, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.

出版信息

J Dent Res. 2018 Jul;97(8):893-900. doi: 10.1177/0022034518760855. Epub 2018 Mar 5.

Abstract

Sjögren syndrome (SS), a chronic autoimmune disorder causing dry mouth, adversely affects the overall oral health in patients. Activation of innate immune responses and excessive production of type I interferons (IFNs) play a critical role in the pathogenesis of this disorder. Recognition of nucleic acids by cytosolic nucleic acid sensors is a major trigger for the induction of type I IFNs. Upon activation, cytosolic DNA sensors can interact with the stimulator of interferon genes (STING) protein, and activation of STING causes increased expression of type I IFNs. The role of STING activation in SS is not known. In this study, to investigate whether the cytosolic DNA sensing pathway influences SS development, female C57BL/6 mice were injected with a STING agonist, dimethylxanthenone-4-acetic acid (DMXAA). Salivary glands (SGs) were studied for gene expression and inflammatory cell infiltration. SG function was evaluated by measuring pilocarpine-induced salivation. Sera were analyzed for cytokines and autoantibodies. Primary SG cells were used to study the expression and activation of STING. Our data show that systemic DMXAA treatment rapidly induced the expression of Ifnb1, Il6, and Tnfa in the SGs, and these cytokines were also elevated in circulation. In contrast, increased Ifng gene expression was dominantly detected in the SGs. The type I innate lymphoid cells present within the SGs were the major source of IFN-γ, and their numbers increased significantly within 3 d of treatment. STING expression in SGs was mainly observed in ductal and interstitial cells. In primary SG cells, DMXAA activated STING and induced IFN-β production. The DMXAA-treated mice developed autoantibodies, sialoadenitis, and glandular hypofunction. Our study demonstrates that activation of the STING pathway holds the potential to initiate SS. Thus, apart from viral infections, conditions that cause cellular perturbations and accumulation of host DNA within the cytosol should also be considered as possible triggers for SS.

摘要

干燥综合征(SS)是一种慢性自身免疫性疾病,可导致口干,对患者的整体口腔健康产生不利影响。先天免疫反应的激活和 I 型干扰素(IFN)的过度产生在这种疾病的发病机制中起着关键作用。细胞质核酸传感器识别核酸是诱导 I 型 IFN 的主要触发因素。激活后,细胞质 DNA 传感器可以与干扰素基因刺激物(STING)蛋白相互作用,STING 的激活导致 I 型 IFN 的表达增加。STING 激活在 SS 中的作用尚不清楚。在这项研究中,为了研究细胞质 DNA 感应途径是否影响 SS 的发展,雌性 C57BL/6 小鼠被注射 STING 激动剂二甲氧蒽酮-4-乙酸(DMXAA)。研究了唾液腺(SGs)的基因表达和炎症细胞浸润。通过测量毛果芸香碱诱导的唾液分泌来评估 SG 功能。分析了血清中的细胞因子和自身抗体。使用原代 SG 细胞研究了 STING 的表达和激活。我们的数据表明,全身 DMXAA 治疗可迅速诱导 SG 中 Ifnb1、Il6 和 Tnfa 的表达,这些细胞因子也在循环中升高。相比之下,SG 中主要检测到 Ifng 基因表达增加。SG 中存在的 I 型固有淋巴细胞是 IFN-γ的主要来源,并且在治疗后 3 天内其数量显著增加。SG 中的 STING 表达主要在导管和间质细胞中观察到。在原代 SG 细胞中,DMXAA 激活 STING 并诱导 IFN-β产生。DMXAA 处理的小鼠产生自身抗体、唾液腺炎和腺体功能减退。我们的研究表明,STING 途径的激活有可能引发 SS。因此,除了病毒感染外,还应将导致细胞紊乱和细胞质中宿主 DNA 积累的情况也视为 SS 的可能触发因素。

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