U1174, INSERM, Orsay, France.
Université Paris-Sud, Orsay, France.
Gut. 2020 Jan;69(1):146-157. doi: 10.1136/gutjnl-2018-316975. Epub 2019 Feb 5.
We explored the hypothesis that TGR5, the bile acid (BA) G-protein-coupled receptor highly expressed in biliary epithelial cells, protects the liver against BA overload through the regulation of biliary epithelium permeability.
Experiments were performed under basal and TGR5 agonist treatment. In vitro transepithelial electric resistance (TER) and FITC-dextran diffusion were measured in different cell lines. In vivo FITC-dextran was injected in the gallbladder (GB) lumen and traced in plasma. Tight junction proteins and TGR5-induced signalling were investigated in vitro and in vivo (wild-type [WT] and TGR5-KO livers and GB). WT and TGR5-KO mice were submitted to bile duct ligation or alpha-naphtylisothiocyanate intoxication under vehicle or TGR5 agonist treatment, and liver injury was studied.
In vitro TGR5 stimulation increased TER and reduced paracellular permeability for dextran. In vivo dextran diffusion after GB injection was increased in TGR5-knock-out (KO) as compared with WT mice and decreased on TGR5 stimulation. In TGR5-KO bile ducts and GB, junctional adhesion molecule A (JAM-A) was hypophosphorylated and selectively downregulated among TJP analysed. TGR5 stimulation induced JAM-A phosphorylation and stabilisation both in vitro and in vivo, associated with protein kinase C-ζ activation. TGR5 agonist-induced TER increase as well as JAM-A protein stabilisation was dependent on JAM-A Ser285 phosphorylation. TGR5 agonist-treated mice were protected from cholestasis-induced liver injury, and this protection was significantly impaired in JAM-A-KO mice.
The BA receptor TGR5 regulates biliary epithelial barrier function in vitro and in vivo through an impact on JAM-A expression and phosphorylation, thereby protecting liver parenchyma against bile leakage.
我们探讨了这样一种假设,即 TGR5 是一种在胆管上皮细胞中高度表达的胆酸(BA)G 蛋白偶联受体,通过调节胆管上皮通透性来保护肝脏免受 BA 过载的影响。
在基础状态和 TGR5 激动剂治疗下进行实验。在不同的细胞系中测量跨上皮电阻(TER)和 FITC-葡聚糖扩散。在体内将 FITC-葡聚糖注入胆囊(GB)腔并在血浆中追踪。在体内和体外(野生型[WT]和 TGR5-KO 肝脏和 GB)研究紧密连接蛋白和 TGR5 诱导的信号转导。WT 和 TGR5-KO 小鼠在载体或 TGR5 激动剂治疗下接受胆管结扎或α-萘基异硫氰酸酯中毒,并研究肝损伤。
体外 TGR5 刺激增加了 TER 并减少了葡聚糖的细胞旁通透性。与 WT 小鼠相比,GB 注射后体内葡聚糖扩散在 TGR5 敲除(KO)中增加,而在 TGR5 刺激下减少。在 TGR5-KO 胆管和 GB 中,连接黏附分子 A(JAM-A)的丝氨酸 285 磷酸化减少,并且在分析的 TJP 中选择性地下调。TGR5 刺激在体内和体外均诱导 JAM-A 磷酸化和稳定,与蛋白激酶 C-ζ 激活相关。TGR5 激动剂诱导的 TER 增加以及 JAM-A 蛋白稳定依赖于 JAM-A Ser285 磷酸化。TGR5 激动剂治疗的小鼠对胆甾醇诱导的肝损伤具有保护作用,而在 JAM-A-KO 小鼠中这种保护作用显著受损。
BA 受体 TGR5 通过影响 JAM-A 的表达和磷酸化来调节胆管上皮细胞的屏障功能,从而保护肝实质免受胆汁泄漏的影响。