Role of Immune Cells in Biliary Repair

被引:17
作者
Lan, Tian [1 ,2 ]
Qian, Shuaijie [1 ,2 ]
Tang, Chengwei [1 ,2 ]
Gao, Jinhang [1 ,2 ]
机构
[1] Sichuan Univ, West China Hosp, Lab Gastroenterol & Hepatol, State Key Lab Biotherapy, Chengdu, Peoples R China
[2] Sichuan Univ, West China Hosp, Dept Gastroenterol, Chengdu, Peoples R China
来源
FRONTIERS IN IMMUNOLOGY | 2022年 / 13卷
基金
国家重点研发计划;
关键词
cholangiopathy; biliary repair; liver progenitor cell; macrophage; hepatocyte-cholangiocyte transdifferentiation; immune cells; LIVER PROGENITOR-CELL; LONG-TERM EXPANSION; HEPATIC STEM-CELLS; EPITHELIAL-CELLS; BONE-MARROW; LARGE CHOLANGIOCYTES; DUCTULAR REACTIONS; CHOLESTATIC LIVER; ADULT LIVER; BILE-DUCTS;
D O I
10.3389/fimmu.2022.866040
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The biliary system is comprised of cholangiocytes and plays an important role in maintaining liver function. Under normal conditions, cholangiocytes remain in the stationary phase and maintain a very low turnover rate. However, the robust biliary repair is initiated in disease conditions, and different repair mechanisms can be activated depending on the pathological changes. During biliary disease, immune cells including monocytes, lymphocytes, neutrophils, and mast cells are recruited to the liver. The cellular interactions between cholangiocytes and these recruited immune cells as well as hepatic resident immune cells, including Kupffer cells, determine disease outcomes. However, the role of immune cells in the initiation, regulation, and suspension of biliary repair remains elusive. The cellular processes of cholangiocyte proliferation, progenitor cell differentiation, and hepatocyte-cholangiocyte transdifferentiation during biliary diseases are reviewed to manifest the underlying mechanism of biliary repair. Furthermore, the potential role of immune cells in crucial biliary repair mechanisms is highlighted. The mechanisms of biliary repair in immune-mediated cholangiopathies, inherited cholangiopathies, obstructive cholangiopathies, and cholangiocarcinoma are also summarized. Additionally, novel techniques that could clarify the underlying mechanisms of biliary repair are displayed. Collectively, this review aims to deepen the understanding of the mechanisms of biliary repair and contributes potential novel therapeutic methods for treating biliary diseases.
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页数:18
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共 209 条
[1]   Sox9 Is a Modifier of the Liver Disease Severity in a Mouse Model of Alagille Syndrome [J].
Adams, Joshua M. ;
Huppert, Kari A. ;
Castro, Eumenia C. ;
Lopez, Mario F. ;
Niknejad, Nima ;
Subramanian, Sanjay ;
Zarrin-Khameh, Neda ;
Finegold, Milton J. ;
Huppert, Stacey S. ;
Jafar-Nejad, Hamed .
HEPATOLOGY, 2020, 71 (04) :1331-1349
[2]   Epigenetic remodelling licences adult cholangiocytes for organoid formation and liver regeneration [J].
Aloia, Luigi ;
McKie, Mikel Alexander ;
Vernaz, Gregoire ;
Cordero-Espinoza, Lucia ;
Aleksieva, Niya ;
van den Ameele, Jelle ;
Antonica, Francesco ;
Font-Cunill, Berta ;
Raven, Alexander ;
Cigliano, Riccardo Aiese ;
Belenguer, German ;
Mort, Richard L. ;
Brand, Andrea H. ;
Zernicka-Goetz, Magdalena ;
Forbes, Stuart J. ;
Miska, Eric A. ;
Huch, Meritxell .
NATURE CELL BIOLOGY, 2019, 21 (11) :1321-+
[3]   Activation of Alpha1-Adrenergic Receptors Stimulate the Growth of Small Mouse Cholangiocytes Via Calcium-Dependent Activation of Nuclear Factor of Activated T Cells 2 and Specificity Protein 1 [J].
Alpini, Gianfranco ;
Franchitto, Antonio ;
DeMorrow, Sharon ;
Onori, Paolo ;
Gaudio, Eugenio ;
Wise, Candace ;
Francis, Heather ;
Venter, Julie ;
Kopriva, Shelley ;
Mancinelli, Romina ;
Carpino, Guido ;
Stagnitti, Franco ;
Ueno, Yoshiyuki ;
Han, Yuyan ;
Meng, Fanyin ;
Glaser, Shannon .
HEPATOLOGY, 2011, 53 (02) :628-639
[4]   Intrahepatic Bile Ducts Develop According to a New Mode of Tubulogenesis Regulated by the Transcription Factor SOX9 [J].
Antoniou, Aline ;
Raynaud, Peggy ;
Cordi, Sabine ;
Zong, Yiwei ;
Tronche, Francois ;
Stanger, Ben Z. ;
Jacquemin, Patrick ;
Pierreux, Christophe E. ;
Clotman, Frederic ;
Lemaigre, Frederic P. .
GASTROENTEROLOGY, 2009, 136 (07) :2325-2333
[5]   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
[6]   Beta-amyloid deposition around hepatic bile ducts is a novel pathobiological and diagnostic feature of biliary atresia [J].
Babu, Rosana Ottakandathil ;
Lui, Vincent Chi Hang ;
Chen, Yan ;
Yiu, Rachel Sze Wan ;
Ye, Yongqin ;
Niu, Ben ;
Wu, Zhongluan ;
Zhang, Ruizhong ;
Yu, Michelle On Na ;
Chung, Patrick Ho Yu ;
Wong, Kenneth Kak Yuen ;
Xia, Huimin ;
Zhang, Michael Qi ;
Wang, Bin ;
Lendahl, Urban ;
Tam, Paul Kwong Hang .
JOURNAL OF HEPATOLOGY, 2020, 73 (06) :1391-1403
[7]   Cholangiocyte pathobiology [J].
Banales, Jesus M. ;
Huebert, Robert C. ;
Karlsen, Tom ;
Strazzabosco, Mario ;
LaRusso, Nicholas F. ;
Gores, Gregory J. .
NATURE REVIEWS GASTROENTEROLOGY & HEPATOLOGY, 2019, 16 (05) :269-281
[8]   Technological Overview of iPS Induction from Human Adult Somatic Cells [J].
Bayart, Emilie ;
Cohen-Haguenauer, Odile .
CURRENT GENE THERAPY, 2013, 13 (02) :73-92
[9]   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
[10]   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