EpCAM and the biology of hepatic stem/progenitor cells
Identifieur interne : 003013 ( Main/Exploration ); précédent : 003012; suivant : 003014EpCAM and the biology of hepatic stem/progenitor cells
Auteurs : Laurent Dollé [Belgique] ; Neil D. Theise [États-Unis] ; Eva Schmelzer [États-Unis] ; Luke Boulter [Royaume-Uni] ; Olivier Gires [Allemagne] ; Leo A. Van Grunsven [Belgique]Source :
- American Journal of Physiology - Gastrointestinal and Liver Physiology [ 0193-1857 ] ; 2014.
Descripteurs français
- KwdFr :
- Animaux, Antigènes néoplasiques (génétique), Antigènes néoplasiques (métabolisme), Cellules souches (anatomopathologie), Cellules souches (métabolisme), Différenciation cellulaire, Foie (anatomopathologie), Foie (métabolisme), Foie (physiopathologie), Humains, Hépatocytes (anatomopathologie), Hépatocytes (métabolisme), Lignage cellulaire, Maladies du foie (anatomopathologie), Maladies du foie (métabolisme), Maladies du foie (physiopathologie), Molécule d'adhérence des cellules épithéliales, Molécules d'adhérence cellulaire (génétique), Molécules d'adhérence cellulaire (métabolisme), Prolifération cellulaire, Régulation de l'expression des gènes au cours du développement, Régénération hépatique, Transduction du signal.
- MESH :
- anatomopathologie : Cellules souches, Foie, Hépatocytes, Maladies du foie.
- génétique : Antigènes néoplasiques, Molécules d'adhérence cellulaire.
- métabolisme : Antigènes néoplasiques, Cellules souches, Foie, Hépatocytes, Maladies du foie, Molécules d'adhérence cellulaire.
- physiopathologie : Foie, Maladies du foie.
- Animaux, Différenciation cellulaire, Humains, Lignage cellulaire, Molécule d'adhérence des cellules épithéliales, Prolifération cellulaire, Régulation de l'expression des gènes au cours du développement, Régénération hépatique, Transduction du signal.
English descriptors
- KwdEn :
- Animals, Antigens, Neoplasm (genetics), Antigens, Neoplasm (metabolism), Cell Adhesion Molecules (genetics), Cell Adhesion Molecules (metabolism), Cell Differentiation, Cell Lineage, Cell Proliferation, Epithelial Cell Adhesion Molecule, Gene Expression Regulation, Developmental, Hepatocytes (metabolism), Hepatocytes (pathology), Humans, Liver (metabolism), Liver (pathology), Liver (physiopathology), Liver Diseases (metabolism), Liver Diseases (pathology), Liver Diseases (physiopathology), Liver Regeneration, Signal Transduction, Stem Cells (metabolism), Stem Cells (pathology).
- MESH :
- chemical , genetics : Antigens, Neoplasm, Cell Adhesion Molecules.
- chemical , metabolism : Antigens, Neoplasm, Cell Adhesion Molecules.
- metabolism : Hepatocytes, Liver, Liver Diseases, Stem Cells.
- pathology : Hepatocytes, Liver, Liver Diseases, Stem Cells.
- physiopathology : Liver, Liver Diseases.
- Animals, Cell Differentiation, Cell Lineage, Cell Proliferation, Epithelial Cell Adhesion Molecule, Gene Expression Regulation, Developmental, Humans, Liver Regeneration, Signal Transduction.
Abstract
Epithelial cell adhesion molecule (EpCAM) is a transmembrane glycoprotein, which is frequently and highly expressed on carcinomas, tumor-initiating cells, selected tissue progenitors, and embryonic and adult stem cells. During liver development, EpCAM demonstrates a dynamic expression, since it can be detected in fetal liver, including cells of the parenchyma, whereas mature hepatocytes are devoid of EpCAM. Liver regeneration is associated with a population of EpCAM-positive cells within ductular reactions, which gradually lose the expression of EpCAM along with maturation into hepatocytes. EpCAM can be switched on and off through a wide panel of strategies to fine-tune EpCAM-dependent functional and differentiative traits. EpCAM-associated functions relate to cell–cell adhesion, proliferation, maintenance of a pluripotent state, regulation of differentiation, migration, and invasion. These functions can be conferred by the full-length protein and/or EpCAM-derived fragments, which are generated upon regulated intramembrane proteolysis. Control by EpCAM therefore not only depends on the presence of full-length EpCAM at cellular membranes but also on varying rates of the formation of EpCAM-derived fragments that have their own regulatory properties and on changes in the association of EpCAM with interaction partners. Thus spatiotemporal localization of EpCAM in immature liver progenitors, transit-amplifying cells, and mature liver cells will decisively impact the regulation of EpCAM functions and might be one of the triggers that contributes to the adaptive processes in stem/progenitor cell lineages. This review will summarize EpCAM-related molecular events and how they relate to hepatobiliary differentiation and regeneration.
Url:
DOI: 10.1152/ajpgi.00069.2014
PubMed: 25477371
PubMed Central: 4329473
Affiliations:
- Allemagne, Belgique, Royaume-Uni, États-Unis
- Bavière, District de Haute-Bavière, Pennsylvanie, Région de Bruxelles-Capitale, Écosse, État de New York
- Bruxelles, Munich
- Université Louis-et-Maximilien de Munich
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Le document en format XML
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<term>Antigens, Neoplasm (genetics)</term>
<term>Antigens, Neoplasm (metabolism)</term>
<term>Cell Adhesion Molecules (genetics)</term>
<term>Cell Adhesion Molecules (metabolism)</term>
<term>Cell Differentiation</term>
<term>Cell Lineage</term>
<term>Cell Proliferation</term>
<term>Epithelial Cell Adhesion Molecule</term>
<term>Gene Expression Regulation, Developmental</term>
<term>Hepatocytes (metabolism)</term>
<term>Hepatocytes (pathology)</term>
<term>Humans</term>
<term>Liver (metabolism)</term>
<term>Liver (pathology)</term>
<term>Liver (physiopathology)</term>
<term>Liver Diseases (metabolism)</term>
<term>Liver Diseases (pathology)</term>
<term>Liver Diseases (physiopathology)</term>
<term>Liver Regeneration</term>
<term>Signal Transduction</term>
<term>Stem Cells (metabolism)</term>
<term>Stem Cells (pathology)</term>
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<keywords scheme="KwdFr" xml:lang="fr"><term>Animaux</term>
<term>Antigènes néoplasiques (génétique)</term>
<term>Antigènes néoplasiques (métabolisme)</term>
<term>Cellules souches (anatomopathologie)</term>
<term>Cellules souches (métabolisme)</term>
<term>Différenciation cellulaire</term>
<term>Foie (anatomopathologie)</term>
<term>Foie (métabolisme)</term>
<term>Foie (physiopathologie)</term>
<term>Humains</term>
<term>Hépatocytes (anatomopathologie)</term>
<term>Hépatocytes (métabolisme)</term>
<term>Lignage cellulaire</term>
<term>Maladies du foie (anatomopathologie)</term>
<term>Maladies du foie (métabolisme)</term>
<term>Maladies du foie (physiopathologie)</term>
<term>Molécule d'adhérence des cellules épithéliales</term>
<term>Molécules d'adhérence cellulaire (génétique)</term>
<term>Molécules d'adhérence cellulaire (métabolisme)</term>
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<term>Régulation de l'expression des gènes au cours du développement</term>
<term>Régénération hépatique</term>
<term>Transduction du signal</term>
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<term>Foie</term>
<term>Hépatocytes</term>
<term>Maladies du foie</term>
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<term>Molécules d'adhérence cellulaire</term>
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<term>Liver</term>
<term>Liver Diseases</term>
<term>Stem Cells</term>
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<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Antigènes néoplasiques</term>
<term>Cellules souches</term>
<term>Foie</term>
<term>Hépatocytes</term>
<term>Maladies du foie</term>
<term>Molécules d'adhérence cellulaire</term>
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<term>Liver</term>
<term>Liver Diseases</term>
<term>Stem Cells</term>
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<term>Maladies du foie</term>
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<term>Liver Diseases</term>
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<term>Cell Differentiation</term>
<term>Cell Lineage</term>
<term>Cell Proliferation</term>
<term>Epithelial Cell Adhesion Molecule</term>
<term>Gene Expression Regulation, Developmental</term>
<term>Humans</term>
<term>Liver Regeneration</term>
<term>Signal Transduction</term>
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<term>Différenciation cellulaire</term>
<term>Humains</term>
<term>Lignage cellulaire</term>
<term>Molécule d'adhérence des cellules épithéliales</term>
<term>Prolifération cellulaire</term>
<term>Régulation de l'expression des gènes au cours du développement</term>
<term>Régénération hépatique</term>
<term>Transduction du signal</term>
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<front><div type="abstract" xml:lang="en"><p>Epithelial cell adhesion molecule (EpCAM) is a transmembrane glycoprotein, which is frequently and highly expressed on carcinomas, tumor-initiating cells, selected tissue progenitors, and embryonic and adult stem cells. During liver development, EpCAM demonstrates a dynamic expression, since it can be detected in fetal liver, including cells of the parenchyma, whereas mature hepatocytes are devoid of EpCAM. Liver regeneration is associated with a population of EpCAM-positive cells within ductular reactions, which gradually lose the expression of EpCAM along with maturation into hepatocytes. EpCAM can be switched on and off through a wide panel of strategies to fine-tune EpCAM-dependent functional and differentiative traits. EpCAM-associated functions relate to cell–cell adhesion, proliferation, maintenance of a pluripotent state, regulation of differentiation, migration, and invasion. These functions can be conferred by the full-length protein and/or EpCAM-derived fragments, which are generated upon regulated intramembrane proteolysis. Control by EpCAM therefore not only depends on the presence of full-length EpCAM at cellular membranes but also on varying rates of the formation of EpCAM-derived fragments that have their own regulatory properties and on changes in the association of EpCAM with interaction partners. Thus spatiotemporal localization of EpCAM in immature liver progenitors, transit-amplifying cells, and mature liver cells will decisively impact the regulation of EpCAM functions and might be one of the triggers that contributes to the adaptive processes in stem/progenitor cell lineages. This review will summarize EpCAM-related molecular events and how they relate to hepatobiliary differentiation and regeneration.</p>
</div>
</front>
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<li>Belgique</li>
<li>Royaume-Uni</li>
<li>États-Unis</li>
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<li>District de Haute-Bavière</li>
<li>Pennsylvanie</li>
<li>Région de Bruxelles-Capitale</li>
<li>Écosse</li>
<li>État de New York</li>
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<li>Munich</li>
</settlement>
<orgName><li>Université Louis-et-Maximilien de Munich</li>
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<country name="États-Unis"><region name="État de New York"><name sortKey="Theise, Neil D" sort="Theise, Neil D" uniqKey="Theise N" first="Neil D." last="Theise">Neil D. Theise</name>
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<name sortKey="Schmelzer, Eva" sort="Schmelzer, Eva" uniqKey="Schmelzer E" first="Eva" last="Schmelzer">Eva Schmelzer</name>
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<country name="Royaume-Uni"><region name="Écosse"><name sortKey="Boulter, Luke" sort="Boulter, Luke" uniqKey="Boulter L" first="Luke" last="Boulter">Luke Boulter</name>
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<country name="Allemagne"><region name="Bavière"><name sortKey="Gires, Olivier" sort="Gires, Olivier" uniqKey="Gires O" first="Olivier" last="Gires">Olivier Gires</name>
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