Department of Medicine, University of California, San Francisco, San Francisco, CA, USA.
Department of Laboratory Medicine, University of California, San Francisco, San Francisco, CA, USA.
Sci Immunol. 2022 Mar 4;7(69):eabj1080. doi: 10.1126/sciimmunol.abj1080.
Inflammation and dysfunction of the extrahepatic biliary tree are common causes of human pathology, including gallstones and cholangiocarcinoma. Despite this, we know little about the local regulation of biliary inflammation. Tuft cells, rare sensory epithelial cells, are particularly prevalent in the mucosa of the gallbladder and extrahepatic bile ducts. Here, we show that biliary tuft cells express a core genetic tuft cell program in addition to a tissue-specific gene signature and, in contrast to small intestinal tuft cells, decreased postnatally, coincident with maturation of bile acid production. Manipulation of enterohepatic bile acid recirculation revealed that tuft cell abundance is negatively regulated by bile acids, including in a model of obstructive cholestasis in which inflammatory infiltration of the biliary tree correlated with loss of tuft cells. Unexpectedly, tuft cell-deficient mice spontaneously displayed an increased gallbladder epithelial inflammatory gene signature accompanied by neutrophil infiltration that was modulated by the microbiome. We propose that biliary tuft cells function as bile acid-sensitive negative regulators of inflammation in biliary tissues and serve to limit inflammation under homeostatic conditions.
肝外胆管的炎症和功能障碍是人类病理学的常见原因,包括胆结石和胆管癌。尽管如此,我们对胆管炎症的局部调节知之甚少。微绒毛细胞是一种罕见的感觉上皮细胞,在胆囊和肝外胆管的黏膜中特别丰富。在这里,我们表明,胆管微绒毛细胞除了具有组织特异性基因特征外,还表达核心的微绒毛细胞基因程序,与小肠微绒毛细胞不同的是,它们在出生后减少,与胆汁酸产生的成熟同时发生。对肠肝胆汁酸再循环的操作表明,微绒毛细胞的丰度受胆汁酸的负调控,包括在阻塞性胆汁淤积的模型中,微绒毛细胞的炎症浸润与微绒毛细胞的丢失相关。出乎意料的是,微绒毛细胞缺陷小鼠自发地表现出增加的胆囊上皮炎症基因特征,伴有中性粒细胞浸润,这种浸润受微生物组的调节。我们提出,胆管微绒毛细胞作为胆汁酸敏感的负调节因子,在胆管组织中发挥作用,并在稳态条件下限制炎症。