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Tight Junction Proteins and the Biology of Hepatobiliary Disease

Authors :
Roehlen, Natascha
Roca Suarez, Armando Andres
El Saghire, Houssein
Saviano, Antonio
Schuster, Catherine
Lupberger, Joachim
Baumert, Thomas F.
Institut de Recherche sur les Maladies Virales et Hépatiques (IVH)
Université de Strasbourg (UNISTRA)-Institut National de la Santé et de la Recherche Médicale (INSERM)
Source :
International Journal of Molecular Sciences, Vol 21, Iss 3, p 825 (2020), International Journal of Molecular Sciences, International Journal of Molecular Sciences, MDPI, 2020, 21 (3), ⟨10.3390/ijms21030825⟩
Publication Year :
2020

Abstract

Tight junctions (TJ) are intercellular adhesion complexes on epithelial cells and composed of integral membrane proteins as well as cytosolic adaptor proteins. Tight junction proteins have been recognized to play a key role in health and disease. In the liver, TJ proteins have several functions: they contribute as gatekeepers for paracellular diffusion between adherent hepatocytes or cholangiocytes to shape the blood-biliary barrier (BBIB) and maintain tissue homeostasis. At non-junctional localizations, TJ proteins are involved in key regulatory cell functions such as differentiation, proliferation, and migration by recruiting signaling proteins in response to extracellular stimuli. Moreover, TJ proteins are hepatocyte entry factors for the hepatitis C virus (HCV)-a major cause of liver disease and cancer worldwide. Perturbation of TJ protein expression has been reported in chronic HCV infection, cholestatic liver diseases as well as hepatobiliary carcinoma. Here we review the physiological function of TJ proteins in the liver and their implications in hepatobiliary diseases. journal article review 2020 Jan 28 2020 01 28 imported

Details

Language :
English
ISSN :
16616596 and 14220067
Database :
OpenAIRE
Journal :
International Journal of Molecular Sciences, Vol 21, Iss 3, p 825 (2020), International Journal of Molecular Sciences, International Journal of Molecular Sciences, MDPI, 2020, 21 (3), ⟨10.3390/ijms21030825⟩
Accession number :
edsair.pmid.dedup....e0ca1ede0dd63a2ff6e9d241de247743