Huang Jun-Jie, Zhuo Jia-Ying, Wang Qian, Sun Yue, Qi Jia-Xin, Wu Juan-Juan, Zhang Yu, Chen Gang, Jiang Peng-Fei, Fan Yan-Yan
Department of Forensic Medicine, Wenzhou Medical University, Higher Education District, Wenzhou, 325035, Zhejiang Province, People's Republic of China.
School of Basic Medical Science, Wenzhou Medical University, Higher Education District, Wenzhou, 325035, Zhejiang Province, People's Republic of China.
Forensic Sci Med Pathol. 2024 Dec;20(4):1155-1165. doi: 10.1007/s12024-024-00818-3. Epub 2024 Apr 23.
Thrombus age determination in fatal venous thromboembolism cases is an important task for forensic pathologists. In this study, we investigated the time-dependent expressions of formyl peptide receptor 2 (FPR2) and Annexin A1 (ANXA1) in a stasis-induced deep vein thrombosis (DVT) murine model, with the aim of obtaining useful information for thrombus age timing. A total of 75 ICR mice were randomly classified into thrombosis group and control group. In thrombosis group, a DVT model was established by ligating the inferior vena cava (IVC) of mice, and thrombosed IVCs were harvested at 1, 3, 5, 7, 10, 14, and 21 days after modeling. In control group, IVCs without thrombosis were taken as control samples. The expressions of FPR2 and ANXA1 during thrombosis were detected using immunohistochemistry and double immunofluorescence staining. Their protein and mRNA levels in the samples were determined by Western blotting and quantitative real-time PCR. The results reveal that FPR2 was predominantly expressed by intrathrombotic neutrophils and macrophages. ANXA1 expression in the thrombi was mainly distributed in neutrophils, endothelial cells of neovessels, and fibroblastic cells. After thrombosis, the expressions of FPR2 and ANXA1 were time-dependently up-regulated. The percentage of FPR2-positive cells and the level of FPR2 protein significantly elevated at 1, 3, 5 and 7 days after IVC ligation as compared to those at 10, 14 and 21 days after ligation (p < 0.05). Moreover, the mRNA level of FPR2 were significantly higher at 5 days than that at the other post-ligation intervals (p < 0.05). Besides, the levels of ANXA1 mRNA and protein peaked at 10 and 14 days after ligation, respectively. A significant increase in the mRNA level of ANXA1 was found at 10 and 14 days as compared with that at the other post-ligation intervals (p < 0.01). Our findings suggest that FPR2 and ANXA1 are promising as useful markers for age estimation of venous thrombi.
在致命性静脉血栓栓塞病例中确定血栓形成时间是法医病理学家的一项重要任务。在本研究中,我们在淤滞诱导的深静脉血栓形成(DVT)小鼠模型中研究了甲酰肽受体2(FPR2)和膜联蛋白A1(ANXA1)的时间依赖性表达,旨在获取有关血栓形成时间的有用信息。总共75只ICR小鼠被随机分为血栓形成组和对照组。在血栓形成组中,通过结扎小鼠下腔静脉(IVC)建立DVT模型,并在建模后1、3、5、7、10、14和21天采集形成血栓的IVC。在对照组中,将未形成血栓的IVC作为对照样本。使用免疫组织化学和双重免疫荧光染色检测血栓形成过程中FPR2和ANXA1的表达。通过蛋白质印迹法和定量实时PCR测定样本中它们的蛋白质和mRNA水平。结果显示,FPR2主要由血栓内的中性粒细胞和巨噬细胞表达。血栓中ANXA1的表达主要分布在中性粒细胞、新生血管的内皮细胞和成纤维细胞中。血栓形成后,FPR2和ANXA1的表达呈时间依赖性上调。与结扎后10、14和21天相比,IVC结扎后1、3、5和7天FPR2阳性细胞百分比和FPR2蛋白水平显著升高(p<0.05)。此外,FPR2的mRNA水平在结扎后5天显著高于其他结扎后时间间隔(p<0.05)。此外,ANXA1的mRNA和蛋白质水平分别在结扎后10天和14天达到峰值。与其他结扎后时间间隔相比,在结扎后10天和14天发现ANXA1的mRNA水平显著增加(p<0.01)。我们的研究结果表明,FPR2和ANXA1有望成为静脉血栓年龄估计的有用标志物。