Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8258502 | Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease | 2018 | 46 Pages |
Abstract
Cholangiocytes, epithelial cells that line the biliary epithelium, are the primary target cells for cholangiopathies including primary sclerosing cholangitis and primary biliary cholangitis. Quiescent cholangiocytes respond to biliary damage and acquire an activated neuroendocrine phenotype to maintain the homeostasis of the liver. The typical response of cholangiocytes is proliferation leading to bile duct hyperplasia, which is a characteristic of cholestatic liver diseases. Current studies have identified various signaling pathways that are associated with cholangiocyte proliferation/loss and liver fibrosis in cholangiopathies using human samples and rodent models. Although recent studies have demonstrated that extracellular vesicles and microRNAs could be mediators that regulate these messenger/receptor axes, further studies are required to confirm their roles. This review summarizes current studies of biliary response and cholangiocyte proliferation during cholestatic liver injury with particular emphasis on the secretin/secretin receptor axis. This article is part of a Special Issue entitled: Cholangiocytes in Health and Diseaseedited by Jesus Banales, Marco Marzioni, Nicholas LaRusso and Peter Jansen.
Keywords
VEGFRANITGPBAR1BDLAE2Pancreatic Duodenal Homeobox-1PDX-1CaMKIP3EVSCholangiocytesCFTRNK-1RIP3RS1PR2PBCSSTR2CCl4G protein-coupled bile acid receptor 1NAFLDGnRHNFATmiRNAsSphingosine 1-phosphate receptor 2GalR1α-naphthylisothiocyanatearylalkylamine N-acetyltransferaseMT1CCAPSCcAMPprimary biliary cholangitisinositol 1,4,5-trisphosphateScTadenosine 3′,5′-cyclic monophosphateNon-alcoholic steatohepatitisBiliary atresiaYAPinterleukinnon-alcoholic fatty liver diseasesExtracellular vesiclescystic fibrosis transmembrane conductance regulatormicroRNAsCAMendoplasmic reticulumnuclear factor of activated T-cellsAANATVascular endothelial growth factorVascular Endothelial Growth Factor (VEGF)Substance PBile DuctsSecretinNash Gonadotropin-releasing hormoneyes-associated proteinbile duct ligationCalmodulinCarbon tetrachloridePrimary sclerosing cholangitisCholangiocarcinomaCalcineurinIP3 receptorVEGF receptorSomatostatin receptorSecretin receptorNeurokinin-1 receptorGalanin receptor 1
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Authors
Keisaku Sato, Fanyin Meng, Thao Giang, Shannon Glaser, Gianfranco Alpini,