Max Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Department of Medicine I, Gastroenterology and Hepatology, University Hospital Carl-Gustav-Carus, Technische Universität Dresden (TU Dresden), Dresden, Germany.
EMBO Rep. 2023 Sep 6;24(9):e57181. doi: 10.15252/embr.202357181. Epub 2023 Jul 31.
Hepatocytes form bile canaliculi that dynamically respond to the signalling activity of bile acids and bile flow. Little is known about their responses to intraluminal pressure. During embryonic development, hepatocytes assemble apical bulkheads that increase the canalicular resistance to intraluminal pressure. Here, we investigate whether they also protect bile canaliculi against elevated pressure upon impaired bile flow in adult liver. Apical bulkheads accumulate upon bile flow obstruction in mouse models and patients with primary sclerosing cholangitis (PSC). Their loss under these conditions leads to abnormally dilated canaliculi, resembling liver cell rosettes described in other hepatic diseases. 3D reconstruction reveals that these structures are sections of cysts and tubes formed by hepatocytes. Mathematical modelling establishes that they positively correlate with canalicular pressure and occur in early PSC stages. Using primary hepatocytes and 3D organoids, we demonstrate that excessive canalicular pressure causes the loss of apical bulkheads and formation of rosettes. Our results suggest that apical bulkheads are a protective mechanism of hepatocytes against impaired bile flow, highlighting the role of canalicular pressure in liver diseases.
肝细胞形成胆小管,这些小管能对胆汁酸和胆汁流动的信号活动做出动态响应。然而,人们对它们对管腔内压力的反应知之甚少。在胚胎发育过程中,肝细胞组装顶端隔板,以增加胆管对管腔内压力的阻力。在这里,我们研究了在成年肝脏胆汁流动受阻时,它们是否也能保护胆小管免受升高的压力。在小鼠模型和原发性硬化性胆管炎 (PSC) 患者中,当胆汁流动受阻时,顶端隔板会积累。在这些条件下,它们的缺失会导致胆小管异常扩张,类似于在其他肝脏疾病中描述的肝细胞玫瑰花结。3D 重建表明,这些结构是由肝细胞形成的囊泡和管腔的切片。数学模型建立表明,它们与胆小管压力呈正相关,并出现在 PSC 的早期阶段。通过使用原代肝细胞和 3D 类器官,我们证明了过度的胆小管压力会导致顶端隔板的丢失和玫瑰花结的形成。我们的结果表明,顶端隔板是肝细胞防止胆汁流动受阻的一种保护机制,突出了管腔内压力在肝脏疾病中的作用。