The First People's Hospital of Changzhou, The Third Affiliated Hospital of Soochow University, Changzhou, Jiangsu 213000, China; Department of General Surgery, Wujin Affiliated Hospital of Jiangsu University and The Wujin clinical college of Xuzhou medical university, Changzhou Key Laboratory of Molecular Diagnostics and Precision Cancer Medicine, Wujin Institute of Molecular Diagnostics and Precision Cancer Medicine of Jiangsu University, Changzhou, Jiangsu 213000, China.
Department of Hepatobiliary Surgery, Kunshan First People's Hospital affiliated to Jiangsu University, Kunshan, Jiangsu 215300, China.
Biochim Biophys Acta Mol Basis Dis. 2024 Aug;1870(6):167266. doi: 10.1016/j.bbadis.2024.167266. Epub 2024 May 26.
Acute cholestatic liver injury (ACLI) is a disease associated with bile duct obstruction that causes liver inflammation and apoptosis. Although G protein-coupled bile acid receptor1 (Gpbar-1) has diverse metabolic roles, its involvement in ACLI-associated immune activation remains unclear. Liver tissues and blood samples from 20 patients with ACLI and 20 healthy individuals were analyzed using biochemical tests, H&E staining, western blotting, and immunohistochemistry to verify liver damage and expression of Gpbar-1. The expression of Gpbar-1, cAMP/PKA signaling, and the NLRP3 inflammasome was tested in wild-type (WT) and Gpbar-1 knockdown (si-Gpbar-1) mice with ACLI induced by bile duct ligation (BDL) and in primary Kupffer cells (KCs) with or without Gpbar-1-siRNA. The results showed that total bile acids and Gpbar-1 expressions were elevated in patients with ACLI. Gpbar-1 knockdown significantly worsened BDL-induced acute hepatic damage, inflammation, and liver apoptosis in vivo. Knockdown of Gpbar-1 heightened KC sensitivity to lipopolysaccharide (LPS) stimulation. Gpbar-1 activation inhibited LPS-induced pro-inflammatory responses in normal KCs but not in Gpbar-1-knockdown KCs. Notably, NLRP3-ASC inflammasome expression was effectively enhanced by Gpbar-1 deficiency. Additionally, Gpbar-1 directly increased intracellular cAMP levels and PKA phosphorylation, thus disrupting the NLRP3-ASC inflammasome. The pro-inflammatory characteristic of Gpbar-1 deficiency was almost neutralized by the NLRP3 inhibitor CY-09. In vitro, M1 polarization was accelerated in LPS-stimulated Gpbar-1-knockdown KCs. Therapeutically, Gpbar-1 deficiency exacerbated BDL-induced ACLI, which could be rescued by inhibition of the NLRP3-ASC inflammasome. Our study reveal that Gpbar-1 may act as a novel immune-mediated regulator of ACLI by inhibiting the NLRP3-ASC inflammasome.
急性胆汁淤积性肝损伤 (ACLI) 是一种与胆管阻塞相关的疾病,可导致肝脏炎症和细胞凋亡。尽管 G 蛋白偶联胆汁酸受体 1 (Gpbar-1) 具有多种代谢作用,但它在 ACLI 相关免疫激活中的作用尚不清楚。采用生化试验、H&E 染色、western blot 和免疫组织化学方法分析了 20 例 ACLI 患者和 20 例健康个体的肝组织和血液样本,以验证肝损伤和 Gpbar-1 的表达。在胆管结扎 (BDL) 诱导的 ACLI 野生型 (WT) 和 Gpbar-1 敲低 (si-Gpbar-1) 小鼠以及用或不用 Gpbar-1-siRNA 的原代枯否细胞 (KCs) 中测试了 Gpbar-1 的表达、cAMP/PKA 信号和 NLRP3 炎性小体。结果表明,ACLI 患者的总胆汁酸和 Gpbar-1 表达升高。Gpbar-1 敲低显著加重 BDL 诱导的急性肝损伤、炎症和肝细胞凋亡。敲低 Gpbar-1 增加了 KC 对脂多糖 (LPS) 刺激的敏感性。Gpbar-1 激活抑制了正常 KCs 中 LPS 诱导的促炎反应,但不抑制 Gpbar-1 敲低 KCs 中的反应。值得注意的是,NLRP3-ASC 炎性小体的表达被 Gpbar-1 缺乏有效增强。此外,Gpbar-1 直接增加细胞内 cAMP 水平和 PKA 磷酸化,从而破坏 NLRP3-ASC 炎性小体。NLRP3 抑制剂 CY-09 几乎中和了 Gpbar-1 缺乏的促炎特征。体外,LPS 刺激的 Gpbar-1 敲低 KCs 中 M1 极化加速。在治疗上,Gpbar-1 缺乏加重 BDL 诱导的 ACLI,NLRP3-ASC 炎性小体的抑制可挽救这一结果。我们的研究表明,Gpbar-1 可能通过抑制 NLRP3-ASC 炎性小体,作为 ACLI 的一种新型免疫介导调节剂发挥作用。