Medizinische Klinik mit Schwerpunkt Hepatologie und Gastroenterologie, Charité-Universitätsmedizin Berlin, Campus Virchow Klinikum, Berlin, Germany.
Gastroenterology. 2013 May;144(5):1116-28. doi: 10.1053/j.gastro.2013.01.055. Epub 2013 Feb 4.
BACKGROUND & AIMS: IgG4-related cholangitis is a chronic inflammatory biliary disease that involves different parts of the pancreatobiliary system, but little is known about its mechanisms of pathogenesis. A T-helper (Th) 2 cell cytokine profile predominates in liver tissues from these patients. We investigated whether Th2 cytokines disrupt the barrier function of biliary epithelial cells (BECs) in patients with IgG4-related cholangitis.
We assessed the Th2 cytokine profile in bile samples and brush cytology samples from 16 patients with IgG4-related cholangitis and respective controls, and evaluated transcription of tight junction (TJ)-associated proteins in primary BECs from these patients. The effect of Th2 cytokines on TJ-mediated BEC barrier function and wound closure was examined by immunoblot, transepithelial resistance, charge-selective Na(+)/Cl(-) permeability, and 4-kDa dextran flux analyses.
Bile samples from patients with IgG4-related cholangitis had significant increases in levels of Th2 cytokines, interleukin (IL)-4, and IL-5. IL-13 was not detected in bile samples, but polymerase chain reaction analysis of whole-brush cytology samples from patients with IgG4-related cholangitis revealed increased levels of IL-13 mRNA, compared with controls. BECs isolated from the brush cytology samples revealed decreased levels of claudin-1 and increased levels of claudin-2 mRNAs. In vitro, IL-4 and IL-13 significantly reduced TJ-associated BEC barrier function by activating claudin-2-mediated paracellular pore pathways. Th2 cytokines also impaired wound closure in BEC monolayers.
Th2 cytokines predominate in bile samples from patients with IgG4-related cholangitis and disrupt the TJ-mediated BEC barrier in vitro. Subsequent increases in biliary leaks might contribute to the pathogenesis of chronic biliary inflammation in these patients.
IgG4 相关胆管炎是一种累及胰胆管系统不同部位的慢性炎症性胆道疾病,但对其发病机制知之甚少。这些患者的肝组织中主要存在 Th2 细胞细胞因子谱。我们研究了 Th2 细胞因子是否会破坏 IgG4 相关胆管炎患者的胆管上皮细胞 (BEC) 的屏障功能。
我们评估了 16 例 IgG4 相关胆管炎患者和相应对照者胆汁样本和刷检细胞学样本中的 Th2 细胞因子谱,并评估了这些患者原代 BEC 中紧密连接 (TJ) 相关蛋白的转录。通过免疫印迹、跨上皮电阻、电荷选择性 Na(+)/Cl(-)通透性和 4-kDa 葡聚糖通量分析,研究了 Th2 细胞因子对 TJ 介导的 BEC 屏障功能和伤口闭合的影响。
IgG4 相关胆管炎患者的胆汁样本中 Th2 细胞因子、白细胞介素 (IL)-4 和 IL-5 水平显著增加。胆汁样本中未检测到 IL-13,但对 IgG4 相关胆管炎患者全刷检细胞学样本的聚合酶链反应分析显示,与对照组相比,IL-13 mRNA 水平增加。从刷检细胞学样本中分离出的 BEC 显示 claudin-1 水平降低,claudin-2 mRNA 水平升高。在体外,IL-4 和 IL-13 通过激活 claudin-2 介导的细胞旁孔途径显著降低 TJ 相关 BEC 屏障功能。Th2 细胞因子也损害了 BEC 单层中的伤口闭合。
Th2 细胞因子在 IgG4 相关胆管炎患者的胆汁样本中占主导地位,并在体外破坏 TJ 介导的 BEC 屏障。随后的胆汁渗漏增加可能导致这些患者的慢性胆道炎症的发病机制。