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Mechanisms of cholangiocyte responses to injury
Authors:Keisaku Sato  Fanyin Meng  Thao Giang  Shannon Glaser  Gianfranco Alpini
Affiliation:1. Research, Central Texas Veterans Health Care System, Temple, TX, United States;2. Scott & White Digestive Disease Research Center, Baylor Scott & White Health, Temple, TX, United States;3. Academic Research Integration, Baylor Scott & White Health, Temple, TX, United States;4. Department of Medicine, Texas A&M Health Science Center, College of Medicine, Temple, TX, United States
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:AANAT  AE2  ?  ANIT  α-naphthylisothiocyanate  BA  biliary atresia  BDL  bile duct ligation  cAMP  adenosine 3′,5′-cyclic monophosphate  CCA  cholangiocarcinoma  4  carbon tetrachloride  CFTR  cystic fibrosis transmembrane conductance regulator  CaM  calmodulin  CaMK  CaM-dependent kinase  CN  calcineurin  ER  endoplasmic reticulum  EVs  extracellular vesicles  GalR1  galanin receptor 1  GnRH  gonadotropin-releasing hormone  1  GnRH receptor 1  GPBAR1  G protein-coupled bile acid receptor 1  IL  interleukin  3  inositol 1,4,5-trisphosphate  3  3  miRNAs  microRNAs  MT1  melatonin 1A  NAFLD  non-alcoholic fatty liver diseases  NASH  non-alcoholic steatohepatitis  NFAT  nuclear factor of activated T-cells  NK-1R  neurokinin-1 receptor  PDX-1  pancreatic duodenal homeobox-1  PBC  primary biliary cholangitis  PSC  primary sclerosing cholangitis  SCT  secretin  SP  substance P  S1PR2  sphingosine 1-phosphate receptor 2  SR  secretin receptor  2  somatostatin receptor  VEGF  vascular endothelial growth factor  VEGFR  VEGF receptor  YAP  Yes-associated protein  Biliary damage  Cholangiocytes  Bile ducts  Ductular reactions
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