BBA - Molecular Basis of Disease, ISSN 0925-4439, 04/2018, Volume 1864, Issue 4, pp. 1220 - 1231
Cholangiocytes are epithelial cells that line the intra- and extrahepatic biliary tree. They serve predominantly to mediate the content of luminal biliary...
Senescence | Proliferation | Cholangiopathies | Apoptosis | Bile | Cholangiocytes | CHOLANGIOCYTE PRIMARY CILIA | BIOCHEMISTRY & MOLECULAR BIOLOGY | INTRAHEPATIC BILE-DUCTS | INHIBITS HEPATIC CYSTOGENESIS | BDL RATS | CELLULAR SENESCENCE | HIGH-DENSITY-LIPOPROTEIN | BIOPHYSICS | GLUCAGON-LIKE PEPTIDE-1 | GENE-EXPRESSION | GROWTH-FACTOR | RECEPTOR AGONIST | Epithelial Cells - metabolism | Humans | Cell Proliferation - physiology | Bile Ducts - physiopathology | Cellular Senescence - physiology | Bile - metabolism | Bile Acids and Salts - metabolism | Epithelial Cells - pathology | MicroRNAs - metabolism | Cilia - metabolism | Bile Ducts - cytology | Animals | Bile Duct Diseases - physiopathology | Signal Transduction - physiology | Apoptosis - physiology | Epithelial Cells - cytology
Senescence | Proliferation | Cholangiopathies | Apoptosis | Bile | Cholangiocytes | CHOLANGIOCYTE PRIMARY CILIA | BIOCHEMISTRY & MOLECULAR BIOLOGY | INTRAHEPATIC BILE-DUCTS | INHIBITS HEPATIC CYSTOGENESIS | BDL RATS | CELLULAR SENESCENCE | HIGH-DENSITY-LIPOPROTEIN | BIOPHYSICS | GLUCAGON-LIKE PEPTIDE-1 | GENE-EXPRESSION | GROWTH-FACTOR | RECEPTOR AGONIST | Epithelial Cells - metabolism | Humans | Cell Proliferation - physiology | Bile Ducts - physiopathology | Cellular Senescence - physiology | Bile - metabolism | Bile Acids and Salts - metabolism | Epithelial Cells - pathology | MicroRNAs - metabolism | Cilia - metabolism | Bile Ducts - cytology | Animals | Bile Duct Diseases - physiopathology | Signal Transduction - physiology | Apoptosis - physiology | Epithelial Cells - cytology
Journal Article
1997, Gastroenterology and hepatology, ISBN 0824794141, Volume 3, ix, 575
Book
Gastroenterology, ISSN 0016-5085, 2004, Volume 127, Issue 5, pp. 1565 - 1577
(a ) Division of Gastroenterology, Ospedali Riuniti di Bergamo, Bergamo, Italy
POLYCYSTIC KIDNEY-DISEASE | HEPATOCYTE GROWTH-FACTOR | CRYPTOSPORIDIUM-PARVUM | NITRIC-OXIDE | LIVER-DISEASE | RAT CHOLANGIOCYTES | KNOCKOUT MICE | GASTROENTEROLOGY & HEPATOLOGY | CHOLANGIOCARCINOMA CELL-LINE | BILE-ACIDS | CHOLANGIOCYTE PROLIFERATION | Animals | Models, Biological | Humans | Bile Ducts, Intrahepatic | Epithelial Cells - pathology | Bile Duct Diseases - classification | Bile Duct Diseases - pathology | Apoptosis | Nitrogen oxide | Platelet-derived growth factor | Transforming growth factors | Gastrointestinal diseases
POLYCYSTIC KIDNEY-DISEASE | HEPATOCYTE GROWTH-FACTOR | CRYPTOSPORIDIUM-PARVUM | NITRIC-OXIDE | LIVER-DISEASE | RAT CHOLANGIOCYTES | KNOCKOUT MICE | GASTROENTEROLOGY & HEPATOLOGY | CHOLANGIOCARCINOMA CELL-LINE | BILE-ACIDS | CHOLANGIOCYTE PROLIFERATION | Animals | Models, Biological | Humans | Bile Ducts, Intrahepatic | Epithelial Cells - pathology | Bile Duct Diseases - classification | Bile Duct Diseases - pathology | Apoptosis | Nitrogen oxide | Platelet-derived growth factor | Transforming growth factors | Gastrointestinal diseases
Journal Article
Annual Review of Immunology, ISSN 0732-0582, 4/2019, Volume 37, Issue 1, pp. 47 - 72
Tuft cells-rare solitary chemosensory cells in mucosal epithelia-are undergoing intense scientific scrutiny fueled by recent discovery of unsuspected...
IL-25 | TRPM5 | POU2F3 | type 2 immunity | tuft cells | chemosensation | STEM-CELLS | DOUBLECORTIN | BILE-DUCT | DISTINCT | BRUSH CELLS | ALPHA-GUSTDUCIN | TASTE RECEPTOR-CELLS | IMMUNOLOGY | TYPE-2 IMMUNITY | CHOLINERGIC CHEMOSENSORY CELLS | BITTER | Neural circuitry
IL-25 | TRPM5 | POU2F3 | type 2 immunity | tuft cells | chemosensation | STEM-CELLS | DOUBLECORTIN | BILE-DUCT | DISTINCT | BRUSH CELLS | ALPHA-GUSTDUCIN | TASTE RECEPTOR-CELLS | IMMUNOLOGY | TYPE-2 IMMUNITY | CHOLINERGIC CHEMOSENSORY CELLS | BITTER | Neural circuitry
Journal Article
Journal of Hepatology, ISSN 0168-8278, 2012, Volume 58, Issue 3, pp. 575 - 582
Summary Cholangiocytes, the cells lining bile ducts, are a heterogenous, highly dynamic population of epithelial cells. While these cells comprise a small...
Gastroenterology and Hepatology | Reactivity | Cholangiopathy | Repair | Cholangiocytes | Biliary | SMALL BILE-DUCTS | CELLS | CRYPTOSPORIDIUM-PARVUM | CELLULAR SENESCENCE | HEDGEHOG | IMMUNE-RESPONSES | TOLL-LIKE RECEPTORS | GASTROENTEROLOGY & HEPATOLOGY | EXPRESSION | PRIMARY SCLEROSING CHOLANGITIS | Epithelial Cells - physiology | Biliary Tract - cytology | Bile Duct Diseases - etiology | Humans | Cystic Fibrosis Transmembrane Conductance Regulator - physiology | Toll-Like Receptors - physiology | Bile Duct Diseases - pathology | Oligomers | Histocompatibility antigens | MicroRNA | Gastrointestinal diseases | Genomics | HLA histocompatibility antigens | Genetic research | Cystic fibrosis | Ursodiol | Liver cirrhosis | Mitogens
Gastroenterology and Hepatology | Reactivity | Cholangiopathy | Repair | Cholangiocytes | Biliary | SMALL BILE-DUCTS | CELLS | CRYPTOSPORIDIUM-PARVUM | CELLULAR SENESCENCE | HEDGEHOG | IMMUNE-RESPONSES | TOLL-LIKE RECEPTORS | GASTROENTEROLOGY & HEPATOLOGY | EXPRESSION | PRIMARY SCLEROSING CHOLANGITIS | Epithelial Cells - physiology | Biliary Tract - cytology | Bile Duct Diseases - etiology | Humans | Cystic Fibrosis Transmembrane Conductance Regulator - physiology | Toll-Like Receptors - physiology | Bile Duct Diseases - pathology | Oligomers | Histocompatibility antigens | MicroRNA | Gastrointestinal diseases | Genomics | HLA histocompatibility antigens | Genetic research | Cystic fibrosis | Ursodiol | Liver cirrhosis | Mitogens
Journal Article
BBA - Molecular Basis of Disease, ISSN 0925-4439, 04/2018, Volume 1864, Issue 4, pp. 1435 - 1443
Prognosis of cholangiocarcinoma, a devastating liver epithelial malignancy characterized by early invasiveness, remains very dismal, though its incidence has...
Cancer-associated fibroblasts | Extracellular matrix | Tumor desmoplasia | Lymphatic endothelial cells | Tumor-associated macrophages | LYSYL OXIDASE | INTRAHEPATIC CHOLANGIOCARCINOMA | STEM-CELLS | BIOCHEMISTRY & MOLECULAR BIOLOGY | MESENCHYMAL TRANSITION | HEPATIC STELLATE CELLS | BIOPHYSICS | LIVER | LYMPHANGIOGENESIS | GROWTH-FACTOR | EXPRESSION | Epithelial Cells - metabolism | Paracrine Communication | Signal Transduction | Stromal Cells - pathology | Humans | Stromal Cells - metabolism | Extracellular Matrix - metabolism | Tumor Microenvironment | Epithelial Cells - pathology | Bile Ducts - cytology | Cell Hypoxia | Cholangiocarcinoma - pathology | Lymphatic Vessels - metabolism | Animals | Neoplasm Invasiveness - pathology | Lymphatic Vessels - pathology | Bile Duct Neoplasms - pathology | Extracellular Matrix - pathology | Bile Ducts - pathology | Disease Models, Animal
Cancer-associated fibroblasts | Extracellular matrix | Tumor desmoplasia | Lymphatic endothelial cells | Tumor-associated macrophages | LYSYL OXIDASE | INTRAHEPATIC CHOLANGIOCARCINOMA | STEM-CELLS | BIOCHEMISTRY & MOLECULAR BIOLOGY | MESENCHYMAL TRANSITION | HEPATIC STELLATE CELLS | BIOPHYSICS | LIVER | LYMPHANGIOGENESIS | GROWTH-FACTOR | EXPRESSION | Epithelial Cells - metabolism | Paracrine Communication | Signal Transduction | Stromal Cells - pathology | Humans | Stromal Cells - metabolism | Extracellular Matrix - metabolism | Tumor Microenvironment | Epithelial Cells - pathology | Bile Ducts - cytology | Cell Hypoxia | Cholangiocarcinoma - pathology | Lymphatic Vessels - metabolism | Animals | Neoplasm Invasiveness - pathology | Lymphatic Vessels - pathology | Bile Duct Neoplasms - pathology | Extracellular Matrix - pathology | Bile Ducts - pathology | Disease Models, Animal
Journal Article
Hepatology, ISSN 0270-9139, 2002, Volume 35, Issue 5, pp. 1256 - 1268
The morbidity and mortality from chronic biliary diseases (i.e., the cholangiopathies) remains substantial. End‐stage liver disease from biliary causes of...
RAT-LIVER | CHOLANGIOCYTES | CELLS | PROTEIN-KINASE | CIRRHOSIS | PROLIFERATION | GROWTH-FACTOR | SECRETION | GASTROENTEROLOGY & HEPATOLOGY | CELLULAR-LOCALIZATION | ACID TRANSPORTER | Animals | Epithelial Cells - metabolism | Bile Duct Diseases - metabolism | Bile Ducts - metabolism | Humans | Epithelial Cells - pathology | Bile Duct Diseases - pathology | Bile Ducts - pathology
RAT-LIVER | CHOLANGIOCYTES | CELLS | PROTEIN-KINASE | CIRRHOSIS | PROLIFERATION | GROWTH-FACTOR | SECRETION | GASTROENTEROLOGY & HEPATOLOGY | CELLULAR-LOCALIZATION | ACID TRANSPORTER | Animals | Epithelial Cells - metabolism | Bile Duct Diseases - metabolism | Bile Ducts - metabolism | Humans | Epithelial Cells - pathology | Bile Duct Diseases - pathology | Bile Ducts - pathology
Journal Article
Journal of Hepatology, ISSN 0168-8278, 2015, Volume 63, Issue 2, pp. 399 - 407
Background & Aims Breast tumor kinase (BRK) augments proliferation and promotes cell survival in breast cancers via interactions with SH2 and SH3...
Gastroenterology and Hepatology | SAM68 | RNA interference | ErbB2 | Tyrosine kinases | Cholangiocarcinoma (CC) | BRK | EGFR | CHOLANGIOCARCINOMA | LOCALIZATION | CYCLOOXYGENASE-2 | CANCER CELLS | SRC | THERAPEUTIC TARGET | GENE FAMILY | GROWTH-FACTOR | GASTROENTEROLOGY & HEPATOLOGY | EXPRESSION | Bile Ducts, Intrahepatic - pathology | Cell Proliferation | Bile Duct Neoplasms - metabolism | Signal Transduction | Neoplasm Proteins - biosynthesis | Humans | Gene Expression Regulation, Neoplastic | Male | Blotting, Western | RNA, Neoplasm | Protein-Tyrosine Kinases - genetics | Bile Ducts, Intrahepatic - metabolism | Cell Line, Tumor | Female | Cell Differentiation | Bile Duct Neoplasms - genetics | Bile Duct Neoplasms - pathology | Neoplasm Proteins - genetics | Protein-Tyrosine Kinases - biosynthesis | Real-Time Polymerase Chain Reaction | Proteins | Antimitotic agents | Tyrosine | Phenols | Breast cancer | Antineoplastic agents
Gastroenterology and Hepatology | SAM68 | RNA interference | ErbB2 | Tyrosine kinases | Cholangiocarcinoma (CC) | BRK | EGFR | CHOLANGIOCARCINOMA | LOCALIZATION | CYCLOOXYGENASE-2 | CANCER CELLS | SRC | THERAPEUTIC TARGET | GENE FAMILY | GROWTH-FACTOR | GASTROENTEROLOGY & HEPATOLOGY | EXPRESSION | Bile Ducts, Intrahepatic - pathology | Cell Proliferation | Bile Duct Neoplasms - metabolism | Signal Transduction | Neoplasm Proteins - biosynthesis | Humans | Gene Expression Regulation, Neoplastic | Male | Blotting, Western | RNA, Neoplasm | Protein-Tyrosine Kinases - genetics | Bile Ducts, Intrahepatic - metabolism | Cell Line, Tumor | Female | Cell Differentiation | Bile Duct Neoplasms - genetics | Bile Duct Neoplasms - pathology | Neoplasm Proteins - genetics | Protein-Tyrosine Kinases - biosynthesis | Real-Time Polymerase Chain Reaction | Proteins | Antimitotic agents | Tyrosine | Phenols | Breast cancer | Antineoplastic agents
Journal Article
Cell Calcium, ISSN 0143-4160, 2014, Volume 55, Issue 6, pp. 317 - 324
Abstract Cytosolic calcium (Cai2+ ) is a second messenger that is important for the regulation of secretion in many types of tissues. Bile duct epithelial...
Advanced Basic Science | Calcium | Secretion | InsP3 receptors | Cholangiocytes | PANCREATIC ACINAR-CELLS | PURINERGIC REGULATION | ISOLATED RAT HEPATOCYTES | BILIARY EPITHELIUM | INOSITOL 1,4,5-TRISPHOSPHATE RECEPTOR | III INSP RECEPTOR | TAUROURSODEOXYCHOLIC ACID | CELL BIOLOGY | HEPATOCYTE GAP-JUNCTIONS | ADENOSINE-TRIPHOSPHATE RELEASE | BICARBONATE SECRETION | Cholestasis - pathology | Epithelial Cells - secretion | Epithelial Cells - metabolism | Cholestasis - metabolism | Calcium - metabolism | Inositol 1,4,5-Trisphosphate Receptors - metabolism | Humans | Epithelial Cells - cytology | Calcium Signaling | Bile Ducts - cytology | Receptors, Cytoplasmic and Nuclear - metabolism | Carbonates
Advanced Basic Science | Calcium | Secretion | InsP3 receptors | Cholangiocytes | PANCREATIC ACINAR-CELLS | PURINERGIC REGULATION | ISOLATED RAT HEPATOCYTES | BILIARY EPITHELIUM | INOSITOL 1,4,5-TRISPHOSPHATE RECEPTOR | III INSP RECEPTOR | TAUROURSODEOXYCHOLIC ACID | CELL BIOLOGY | HEPATOCYTE GAP-JUNCTIONS | ADENOSINE-TRIPHOSPHATE RELEASE | BICARBONATE SECRETION | Cholestasis - pathology | Epithelial Cells - secretion | Epithelial Cells - metabolism | Cholestasis - metabolism | Calcium - metabolism | Inositol 1,4,5-Trisphosphate Receptors - metabolism | Humans | Epithelial Cells - cytology | Calcium Signaling | Bile Ducts - cytology | Receptors, Cytoplasmic and Nuclear - metabolism | Carbonates
Journal Article
Journal of Hepatology, ISSN 0168-8278, 2014, Volume 61, Issue 6, pp. 1337 - 1343
Background & Aims Both hepatocytes and cholangiocytes release ATP into the bile, where it acts as a potent autocrine/paracrine stimulus that activates biliary...
Gastroenterology and Hepatology | Nucleoside transporters | Adenosine | Purinergic signalling | Cholangiocytes | CELLS | CHOLANGIOCYTE PRIMARY CILIA | AIRWAY EPITHELIA | RELEASE | RAT CHOLANGIOCYTES | NUCLEOTIDES | GASTROENTEROLOGY & HEPATOLOGY | ATP | EXPRESSION | BICARBONATE SECRETION | BILE | Receptors, Purinergic - physiology | Cells, Cultured | Rats | Receptor, Adenosine A2A - physiology | Cyclic AMP Response Element-Binding Protein - physiology | Receptor Cross-Talk - physiology | Membrane Transport Proteins - physiology | Bile Ducts - cytology | Bile Ducts - physiology | Cyclic AMP - physiology | Epithelial Cells - physiology | Cyclic AMP-Dependent Protein Kinases - physiology | Animals | Models, Animal | Epithelial Cells - cytology | Extracellular Signal-Regulated MAP Kinases - physiology
Gastroenterology and Hepatology | Nucleoside transporters | Adenosine | Purinergic signalling | Cholangiocytes | CELLS | CHOLANGIOCYTE PRIMARY CILIA | AIRWAY EPITHELIA | RELEASE | RAT CHOLANGIOCYTES | NUCLEOTIDES | GASTROENTEROLOGY & HEPATOLOGY | ATP | EXPRESSION | BICARBONATE SECRETION | BILE | Receptors, Purinergic - physiology | Cells, Cultured | Rats | Receptor, Adenosine A2A - physiology | Cyclic AMP Response Element-Binding Protein - physiology | Receptor Cross-Talk - physiology | Membrane Transport Proteins - physiology | Bile Ducts - cytology | Bile Ducts - physiology | Cyclic AMP - physiology | Epithelial Cells - physiology | Cyclic AMP-Dependent Protein Kinases - physiology | Animals | Models, Animal | Epithelial Cells - cytology | Extracellular Signal-Regulated MAP Kinases - physiology
Journal Article
Hepatology, ISSN 0270-9139, 11/2006, Volume 44, Issue 5, pp. 1231 - 1239
Biliary atresia is an inflammatory fibrosclerosing lesion of the bile ducts that leads to biliary cirrhosis and is the most frequent indication for liver...
IN-VITRO | NOD MICE | OBSTRUCTION | INFANTS | DISEASE | CD4(+) | PROLIFERATION | HLA | GASTROENTEROLOGY & HEPATOLOGY | T-CELLS | IMMUNOHISTOCHEMISTRY | Biliary Atresia - etiology | T-Lymphocytes - physiology | Rotavirus | Biliary Atresia - immunology | Autoantigens - blood | Adoptive Transfer | Interferon-gamma - metabolism | Mice, SCID | Reverse Transcriptase Polymerase Chain Reaction | CD4-Positive T-Lymphocytes - physiology | Biliary Atresia - pathology | Autoimmunity - physiology | Epithelium - immunology | Animals | CD3 Complex - immunology | Female | Mice | Mice, Inbred BALB C | In Vitro Techniques | Bile Ducts - immunology | Bile Ducts - pathology | Disease Models, Animal
IN-VITRO | NOD MICE | OBSTRUCTION | INFANTS | DISEASE | CD4(+) | PROLIFERATION | HLA | GASTROENTEROLOGY & HEPATOLOGY | T-CELLS | IMMUNOHISTOCHEMISTRY | Biliary Atresia - etiology | T-Lymphocytes - physiology | Rotavirus | Biliary Atresia - immunology | Autoantigens - blood | Adoptive Transfer | Interferon-gamma - metabolism | Mice, SCID | Reverse Transcriptase Polymerase Chain Reaction | CD4-Positive T-Lymphocytes - physiology | Biliary Atresia - pathology | Autoimmunity - physiology | Epithelium - immunology | Animals | CD3 Complex - immunology | Female | Mice | Mice, Inbred BALB C | In Vitro Techniques | Bile Ducts - immunology | Bile Ducts - pathology | Disease Models, Animal
Journal Article