Ductular Reaction in Liver Diseases: Pathological Mechanisms and Translational Significances

被引:297
作者
Sato, Keisaku [1 ,2 ,3 ]
Marzioni, Marco [4 ]
Meng, Fanyin [1 ,3 ,5 ]
Francis, Heather [1 ,2 ,3 ]
Glaser, Shannon [1 ,2 ,3 ]
Alpini, Gianfranco [1 ,2 ,3 ]
机构
[1] Cent Texas Vet Hlth Care Syst, Res, Temple, TX USA
[2] Texas A&M Hlth Sci Ctr, Coll Med, Dept Med Physiol, Temple, TX USA
[3] Baylor Scott & White Healthcare, Baylor Scott & White Digest Dis Res Ctr, Temple, TX USA
[4] Univ Politecn Marche, Osped Riuniti, Univ Hosp, Clin Gastroenterol & Hepatol, Ancona, Italy
[5] Baylor Scott & White Healthcare, Acad Res Integrat, Temple, TX USA
关键词
HEPATIC PROGENITOR CELLS; BILIARY TREE; ADULT LIVER; STEM-CELLS; SCLEROSING CHOLANGITIS; RAT HEPATOCYTES; STELLATE CELLS; FINER BRANCHES; BETA-CATENIN; MOUSE MODEL;
D O I
10.1002/hep.30150
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Ductular reaction (DR) is characterized by the proliferation of reactive bile ducts induced by liver injuries. DR is pathologically recognized as bile duct hyperplasia and is commonly observed in biliary disorders. It can also be identified in various liver disorders including nonalcoholic fatty liver disease. DR is associated with liver fibrosis and damage, and the extent of DR parallels to patient mortality. DR raises scientific interests because it is associated with transdifferentiation of liver cells and may play an important role in hepatic regeneration. The origin of active cells during DR can be cholangiocytes, hepatocytes, or hepatic progenitor cells, and associated signaling pathways could differ depending on the specific liver injury or animal models used in the study. Although further studies are needed to elucidate detailed mechanisms and the functional roles in liver diseases, DR can be a therapeutic target to inhibit liver fibrosis and to promote liver regeneration. This review summarizes previous studies of DR identified in patients and animal models as well as currently understood mechanisms of DR.
引用
收藏
页码:420 / 430
页数:11
相关论文
共 72 条
[1]   Heterogeneity of the proliferative capacity of rat cholangiocytes after bile duct ligation [J].
Alpini, G ;
Glaser, SS ;
Ueno, Y ;
Pham, L ;
Podila, PV ;
Caligiuri, A ;
LeSage, G ;
LaRusso, NF .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1998, 274 (04) :G767-G775
[2]   Wnt/β-catenin signaling mediates oval cell response in rodents [J].
Apte, Udayan ;
Thompson, Michael D. ;
Cui, Shanshan ;
Liu, Bowen ;
Cieply, Benjamin ;
Monga, Satdarshan P. S. .
HEPATOLOGY, 2008, 47 (01) :288-295
[3]   Yes-associated protein regulates the hepatic response after bile duct ligation [J].
Bai, Haibo ;
Zhang, Nailing ;
Xu, Yang ;
Chen, Qian ;
Khan, Mehtab ;
Potter, James J. ;
Nayar, Suresh K. ;
Cornish, Toby ;
Alpini, Gianfranco ;
Bronk, Steven ;
Pan, Duojia ;
Anders, Robert A. .
HEPATOLOGY, 2012, 56 (03) :1097-1107
[4]   Bone marrow injection stimulates hepatic ductular reactions in the absence of injury via macrophage-mediated TWEAK signaling [J].
Bird, Thomas G. ;
Lu, Wei-Yu ;
Boulter, Luke ;
Gordon-Keylock, Sabrina ;
Ridgway, Rachel A. ;
Williams, Michael J. ;
Taube, Jessica ;
Thomas, James A. ;
Wojtacha, Davina ;
Gambardella, Adriana ;
Sansom, Owen J. ;
Iredale, John P. ;
Forbes, Stuart J. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2013, 110 (16) :6542-6547
[5]   WNT signaling drives cholangiocarcinoma growth and can be pharmacologically inhibited [J].
Boulter, Luke ;
Guest, Rachel V. ;
Kendall, Timothy J. ;
Wilson, David H. ;
Wojtacha, Davina ;
Robson, Andrew J. ;
Ridgway, Rachel A. ;
Samuel, Kay ;
Van Rooijen, Nico ;
Barry, Simon T. ;
Wigmore, Stephen J. ;
Sansom, Owen J. ;
Forbes, Stuart J. .
JOURNAL OF CLINICAL INVESTIGATION, 2015, 125 (03) :1269-1285
[6]   Macrophage-derived Wnt opposes Notch signaling to specify hepatic progenitor cell fate in chronic liver disease [J].
Boulter, Luke ;
Govaere, Olivier ;
Bird, Tom G. ;
Radulescu, Sorina ;
Ramachandran, Prakash ;
Pellicoro, Antonella ;
Ridgway, Rachel A. ;
Seo, Sang Soo ;
Spee, Bart ;
Van Rooijen, Nico ;
Sansom, Owen J. ;
Iredale, John P. ;
Lowell, Sally ;
Roskams, Tania ;
Forbes, Stuart J. .
NATURE MEDICINE, 2012, 18 (04) :572-579
[7]   Peritumoral ductular reaction is related to nuclear translocation of β-catenin in hepatocellular carcinoma [J].
Cai, Xiaobo ;
Li, Feng ;
Zhang, QingQing ;
Xu, Mingyi ;
Qu, Ying ;
Wan, Xinjian ;
Gao, Chunfang ;
Lu, Lungen .
BIOMEDICINE & PHARMACOTHERAPY, 2015, 76 :11-16
[8]   Multipotent Stem/Progenitor Cells in Human Biliary Tree Give Rise to Hepatocytes, Cholangiocytes, and Pancreatic Islets [J].
Cardinale, Vincenzo ;
Wang, Yunfang ;
Carpino, Guido ;
Cui, Cai-Bin ;
Gatto, Manuela ;
Rossi, Massimo ;
Berloco, Pasquale Bartolomeo ;
Cantafora, Alfredo ;
Wauthier, Eliane ;
Furth, Mark E. ;
Inverardi, Luca ;
Dominguez-Bendala, Juan ;
Ricordi, Camillo ;
Gerber, David ;
Gaudio, Eugenio ;
Alvaro, Domenico ;
Reid, Lola .
HEPATOLOGY, 2011, 54 (06) :2159-2172
[9]   An IL-13 inhibitor blocks the development of hepatic fibrosis during a T-helper type 2-dominated inflammatory response [J].
Chiaramonte, MG ;
Donaldson, DD ;
Cheever, AW ;
Wynn, TA .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 104 (06) :777-785
[10]   Fibrosis correlates with a ductular reaction in hepatitis C: Roles of impaired replication, progenitor cells and steatosis [J].
Clouston, AD ;
Powell, EE ;
Walsh, MJ ;
Richardson, MM ;
Demetris, AJ ;
Jonsson, JR .
HEPATOLOGY, 2005, 41 (04) :809-818