Department of Medical Genetics, Iuliu Hațieganu University of Medicine and Pharmacy, 400349 Cluj-Napoca, Romania; Department of Internal Medicine and Radboud Institute for Molecular Life Sciences (RIMLS), Radboud University Medical Centre, 6525GA Nijmegen, The Netherlands.
Department of Internal Medicine and Radboud Institute for Molecular Life Sciences (RIMLS), Radboud University Medical Centre, 6525GA Nijmegen, The Netherlands.
Joint Bone Spine. 2024 May;91(3):105698. doi: 10.1016/j.jbspin.2024.105698. Epub 2024 Feb 1.
Hyperuricaemia is necessary for gout. High urate concentrations have been linked to inflammation in mononuclear cells. Here, we explore the role of the suppressor of cytokine signaling 3 (SOCS3) in urate-induced inflammation.
Peripheral blood mononuclear cells (PBMCs) from gout patients, hyperuricemic and normouricemic individuals were cultured for 24h with varying concentrations of soluble urate, followed by 24h restimulation with lipopolysaccharides (LPS)±monosodium urate (MSU) crystals. Transcriptomic profiling was performed using RNA-Sequencing. DNA methylation was assessed using Illumina Infinium® MethylationEPIC BeadChip system (EPIC array). Phosphorylation of signal transducer and activator of transcription 3 (STAT3) was determined by flow cytometry. Cytokine responses were also assessed in PBMCs from patients with JAK2 V617F tyrosine kinase mutation.
PBMCs pre-treated with urate produced more interleukin-1beta (IL-1β) and interleukin-6 (IL-6) and less interleukin-1 receptor anatagonist (IL-1Ra) after LPS simulation. In vitro, urate treatment enhanced SOCS3 expression in control monocytes but no DNA methylation changes were observed at the SOCS3 gene. A dose-dependent reduction in phosphorylated STAT3 concomitant with a decrease in IL-1Ra was observed with increasing concentrations of urate. PBMCs with constitutively activated STAT3 (JAK2 V617F mutation) could not be primed by urate.
In vitro, urate exposure increased SOCS3 expression, while urate priming, and subsequent stimulation resulted in decreased STAT3 phosphorylation and IL-1Ra production. There was no evidence that DNA methylation constitutes a regulatory mechanism of SOCS3. Elevated SOCS3 and reduced pSTAT3 could play a role in urate-induced hyperinflammation since urate priming had no effect in PBMCs from patients with constitutively activated STAT3.
高尿酸血症是痛风的必要条件。高尿酸浓度与单核细胞中的炎症有关。在这里,我们探讨了细胞因子信号转导抑制因子 3(SOCS3)在尿酸诱导的炎症中的作用。
培养痛风患者、高尿酸血症和正常尿酸血症个体的外周血单核细胞(PBMC)24 小时,然后用不同浓度的可溶性尿酸孵育 24 小时,然后用脂多糖(LPS)+单钠尿酸盐(MSU)晶体再刺激 24 小时。使用 RNA 测序进行转录组分析。使用 Illumina Infinium® MethylationEPIC BeadChip 系统(EPIC 阵列)评估 DNA 甲基化。通过流式细胞术测定信号转导和转录激活因子 3(STAT3)的磷酸化。还评估了 JAK2 V617F 酪氨酸激酶突变患者 PBMC 中的细胞因子反应。
尿酸预处理的 PBMC 在 LPS 模拟后产生更多的白细胞介素-1β(IL-1β)和白细胞介素-6(IL-6),产生更少的白细胞介素-1 受体拮抗剂(IL-1Ra)。体外,尿酸处理增强了对照单核细胞中的 SOCS3 表达,但在 SOCS3 基因上没有观察到 DNA 甲基化变化。随着尿酸浓度的增加,观察到磷酸化 STAT3 呈剂量依赖性减少,同时 IL-1Ra 减少。具有组成型激活 STAT3(JAK2 V617F 突变)的 PBMC 不能被尿酸启动。
在体外,尿酸暴露增加 SOCS3 表达,而尿酸启动和随后的刺激导致 STAT3 磷酸化和 IL-1Ra 产生减少。没有证据表明 DNA 甲基化构成 SOCS3 的调节机制。升高的 SOCS3 和降低的 pSTAT3 可能在尿酸诱导的高炎症中发挥作用,因为尿酸启动对具有组成型激活 STAT3 的 PBMC 没有影响。