Peribiliary Glands Are Key in Regeneration of the Human Biliary Epithelium After Severe Bile Duct Injury.
Journal
Hepatology (Baltimore, Md.)
ISSN: 1527-3350
Titre abrégé: Hepatology
Pays: United States
ID NLM: 8302946
Informations de publication
Date de publication:
04 2019
04 2019
Historique:
received:
02
07
2018
accepted:
07
11
2018
pubmed:
7
12
2018
medline:
30
5
2020
entrez:
4
12
2018
Statut:
ppublish
Résumé
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.
Identifiants
pubmed: 30506902
doi: 10.1002/hep.30365
pmc: PMC6594148
doi:
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1719-1734Subventions
Organisme : ZonMW grands
ID : 114025003
Pays : International
Organisme : Sapienza University of Rome
ID : 114021010
Pays : International
Organisme : Vesta Therapeutics
Pays : International
Organisme : Cock-Hadders Stichting
Pays : International
Organisme : ZonMW
ID : 114025003
Pays : International
Organisme : ZonMW
ID : 114021010
Pays : International
Organisme : de Cock-Hadders Stichting, University Medical Center Groningen
Pays : International
Informations de copyright
© 2018 The Authors. Hepatology published by Wiley Periodicals, Inc., on behalf of American Association for the Study of Liver Diseases.
Références
Semin Liver Dis. 2002 Aug;22(3):227-40
pubmed: 12360417
J Pathol Bacteriol. 1961 Jul;82:83-94
pubmed: 13716124
Am J Physiol Gastrointest Liver Physiol. 2006 Aug;291(2):G307-17
pubmed: 16574985
Gastroenterology. 2006 Apr;130(4):1270-82
pubmed: 16618418
World J Gastroenterol. 2006 Jun 14;12(22):3523-36
pubmed: 16773709
Stem Cells Dev. 2007 Dec;16(6):979-87
pubmed: 18004941
Cell Death Differ. 2008 Apr;15(4):621-7
pubmed: 18259201
Lab Invest. 2009 Apr;89(4):456-69
pubmed: 19204666
Hepatology. 2011 Jan;53(1):293-305
pubmed: 21254177
Hepatology. 2011 Dec;54(6):2159-72
pubmed: 21809358
J Anat. 2012 Feb;220(2):186-99
pubmed: 22136171
Liver Int. 2012 Apr;32(4):554-9
pubmed: 22171992
Hepatology. 2013 Feb;57(2):775-84
pubmed: 22996260
Mutat Res. 2013 Jan-Mar;752(1):25-35
pubmed: 23010441
J Hepatol. 2013 Jun;58(6):1252-3
pubmed: 23336979
Hepatology. 2013 Oct;58(4):1486-1496
pubmed: 23703727
Exp Biol Med (Maywood). 2013 May;238(5):549-65
pubmed: 23856906
World J Hepatol. 2013 Aug 27;5(8):425-32
pubmed: 24023981
Histol Histopathol. 2014 Jan;29(1):1-10
pubmed: 24108502
Gastroenterology. 2014 Feb;146(2):349-56
pubmed: 24315991
J Hepatol. 2014 Jun;60(6):1172-9
pubmed: 24560661
J Hepatol. 2015 Nov;63(5):1220-8
pubmed: 26119688
Nat Biotechnol. 2015 Aug;33(8):853-61
pubmed: 26167630
Hepatology. 2016 Jul;64(1):277-86
pubmed: 26524612
J Anat. 2016 Mar;228(3):474-86
pubmed: 26610370
Radiographics. 2016 Mar-Apr;36(2):374-92
pubmed: 26824512
Nat Cell Biol. 2016 Mar;18(3):246-54
pubmed: 26911908
Eur J Pharmacol. 2016 Nov 5;790:57-61
pubmed: 27375078
Proc Natl Acad Sci U S A. 2017 May 9;114(19):E3806-E3815
pubmed: 28439013
Mol Cell. 2017 May 4;66(3):306-319
pubmed: 28475867
Am J Physiol Gastrointest Liver Physiol. 2017 Aug 1;313(2):G102-G116
pubmed: 28526690
Br J Pharmacol. 2017 Sep;174(18):3107-3117
pubmed: 28691737
Biochim Biophys Acta Mol Basis Dis. 2018 Apr;1864(4 Pt B):1524-1531
pubmed: 28778591
Am J Pathol. 2018 Mar;188(3):627-639
pubmed: 29248458
J Pathol. 1979 Aug;128(4):213-20
pubmed: 521865