Zhao Yue, Liang Bin, Sheng Shuyang, Wang Chen, Jin Bingyu, Zhang Xiaokang, Cheng Yating, Shen Changxin, Zheng Fang
Center for Gene Diagnosis and Department of Clinical Laboratory Medicine, Zhongnan Hospital of Wuhan University, Wuhan, China.
Department of Clinical Laboratory, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Immun Inflamm Dis. 2024 Jun;12(6):e1317. doi: 10.1002/iid3.1317.
Numerous studies have demonstrated that Absent in Melanoma 2 (AIM2) is upregulated in aortic plaques, especially in Vascular Smooth Muscle Cells in Coronary Artery Disease (CAD), and is related to inflammasome-induced inflammation. However, the underlying mechanism of this phenomenon and the role of AIM2 in atherosclerosis remained unclear.
This study enrolled 133 CAD patients and 123 controls. We isolated Peripheral Blood Leukocytes (PBLs) and the mRNA expression of AIM2 inflammasome and its downstream genes (ASC, Caspase-1, IL-1β, and IL-18) were detected by real-time quantitative PCR (qPCR). We assessed correlations between AIM2 expressions and clinical characteristics by multiple linear regression and spearman's correlation. The THP-1 cells cultured in poly(dA:dT), A151, interferon-gamma (IFN-γ), AG490, or JC2-11. And then the mRNA and protein levels of AIM2, ASC, Caspase-1, IL-1β, IL-18, GSDMD, and STAT1 were analyzed by qPCR and Western blot analysis, respectively. The migration and adhesive capacity of THP-1 cells was assessed using an inverted microscope and an inverted fluorescence microscope, respectively.
In this study, we found that expressions of components of AIM2 inflammasome and its downstream genes (ASC, Caspase-1, IL-1β, and IL-18), were all increased in PBLs of CAD patients, which indicated the inflammasome activation. AIM2 inflammasome activation further induced pyroptosis, and stimulated migration and adhesion in monocyte cell lines, which was regulated by IFN-γ probably through JAK2/STAT1 pathway. In addition, AIM2 expressions were positively correlated with systemic inflammatory indicators as an independent risk factor for CAD.
In conclusion, increased AIM2 expression, induced by the IFN-γ/JAK2/STAT1 signal, orientates monocytes to inflammatory status or even pyroptosis through AIM2 inflammasome activation, which is involved in the development of CAD.
大量研究表明,黑色素瘤缺失2(AIM2)在主动脉斑块中上调,尤其是在冠状动脉疾病(CAD)的血管平滑肌细胞中,并且与炎性小体诱导的炎症有关。然而,这一现象的潜在机制以及AIM2在动脉粥样硬化中的作用仍不清楚。
本研究纳入了133例CAD患者和123例对照。我们分离外周血白细胞(PBLs),并通过实时定量PCR(qPCR)检测AIM2炎性小体及其下游基因(ASC、半胱天冬酶-1、白细胞介素-1β和白细胞介素-18)的mRNA表达。我们通过多元线性回归和斯皮尔曼相关性分析评估AIM2表达与临床特征之间的相关性。将THP-1细胞培养于聚(dA:dT)、A151、干扰素-γ(IFN-γ)、AG490或JC2-11中。然后分别通过qPCR和蛋白质免疫印迹分析检测AIM2、ASC、半胱天冬酶-1、白细胞介素-1β、白细胞介素-18、Gasdermin D(GSDMD)和信号转导子和转录激活子1(STAT1)的mRNA和蛋白质水平。分别使用倒置显微镜和倒置荧光显微镜评估THP-1细胞的迁移和黏附能力。
在本研究中,我们发现CAD患者PBLs中AIM2炎性小体及其下游基因(ASC、半胱天冬酶-1、白细胞介素-1β和白细胞介素-18)的表达均增加,这表明炎性小体激活。AIM2炎性小体激活进一步诱导细胞焦亡,并刺激单核细胞系的迁移和黏附,这可能通过JAK2/STAT1途径由IFN-γ调节。此外,AIM2表达与全身炎症指标呈正相关,是CAD的独立危险因素。
总之,由IFN-γ/JAK2/STAT1信号诱导的AIM2表达增加,通过AIM2炎性小体激活使单核细胞趋向炎症状态甚至细胞焦亡,这参与了CAD的发生发展。