Peribiliary Glands Are Key in Regeneration of the Human Biliary Epithelium After Severe Bile Duct Injury

被引:49
作者
de Jong, Iris E. M. [1 ,2 ]
Matton, Alix P. M. [1 ,2 ]
van Praagh, Jasper B. [2 ,3 ]
van Haaften, Wouter T. [3 ]
Wiersema-Buist, Janneke [2 ]
van Wijk, Louise A. [3 ]
Oosterhuis, Dorenda [3 ]
Iswandana, Raditya [3 ,4 ]
Suriguga, Su [3 ]
Overi, Diletta [5 ]
Lisman, Ton [2 ]
Carpino, Guido [6 ]
Gouw, Annette S. H. [7 ]
Olinga, Peter [3 ]
Gaudio, Eugenio [5 ]
Porte, Robert J. [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Surg, Sect Hepatobiliary Surg & Liver Transplantat, Groningen, Netherlands
[2] Univ Groningen, Univ Med Ctr Groningen, Dept Surg, Surg Res Lab, Groningen, Netherlands
[3] Univ Groningen, Dept Pharmaceut Technol & Biopharm, Groningen, Netherlands
[4] Univ Indonesia, Fac Pharm, Depok, Indonesia
[5] Sapienza Univ Rome, Dept Anat Histol Forens Med & Orthoped Sci, Rome, Italy
[6] Univ Rome Foro Italico, Div Hlth Sci, Dept Movement Human & Hlth Sci, Rome, Italy
[7] Univ Groningen, Univ Med Ctr Groningen, Dept Pathol, Groningen, Netherlands
关键词
HEPATIC STEM-CELLS; FUNCTIONAL-HETEROGENEITY; STEM/PROGENITOR CELLS; TREE; REPAIR; MODEL; DIFFERENTIATION; TRANSPLANTATION; CHOLANGIOCYTES; ACTIVATION;
D O I
10.1002/hep.30365
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Peribiliary glands (PBG) are a source of stem/progenitor cells organized in a cellular network encircling large bile ducts. Severe cholangiopathy with loss of luminal biliary epithelium has been proposed to activate PBG, resulting in cell proliferation and differentiation to restore biliary epithelial integrity. However, formal evidence for this concept in human livers is lacking. We therefore developed an ex vivo model using precision-cut slices of extrahepatic human bile ducts obtained from discarded donor livers, providing an intact anatomical organization of cell structures, to study spatiotemporal differentiation and migration of PBG cells after severe biliary injury. Postischemic bile duct slices were incubated in oxygenated culture medium for up to a week. At baseline, severe tissue injury was evident with loss of luminal epithelial lining and mural stroma necrosis. In contrast, PBG remained relatively well preserved and different reactions of PBG were noted, including PBG dilatation, cell proliferation, and maturation. Proliferation of PBG cells increased after 24 hours of oxygenated incubation, reaching a peak after 72 hours. Proliferation of PBG cells was paralleled by a reduction in PBG apoptosis and differentiation from a primitive and pluripotent (homeobox protein Nanog+/ sex-determining region Y-box 9+) to a mature (cystic fibrosis transmembrane conductance regulator+/secretin receptor+) and activated phenotype (increased expression of hypoxia-inducible factor 1 alpha, glucose transporter 1, and vascular endothelial growth factor A). Migration of proliferating PBG cells in our ex vivo model was unorganized, but resulted in generation of epithelial monolayers at stromal surfaces. Conclusion: Human PBG contain biliary progenitor cells and are able to respond to bile duct epithelial loss with proliferation, differentiation, and maturation to restore epithelial integrity. The ex vivo spatiotemporal behavior of human PBG cells provides evidence for a pivotal role of PBG in biliary regeneration after severe injury.
引用
收藏
页码:1719 / 1734
页数:16
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