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Verfasst von:Breitkopf-Heinlein, Katja [VerfasserIn]   i
 Martinez-Chantar, Maria Luz [VerfasserIn]   i
Titel:Targeting hepatic stellate cells to combat liver fibrosis
Titelzusatz:where do we stand?
Verf.angabe:Katja Breitkopf-Heinlein, Maria Luz Martinez-Chantar
E-Jahr:2024
Jahr:August 08, 2024
Umfang:3 S.
Illustrationen:Illustrationen
Fussnoten:Online verfügbar: 25. April 2024, Artikelversion: 8. August 2024 ; Gesehen am 19.08.2024
Titel Quelle:Enthalten in: Gut
Ort Quelle:London : BMJ Publishing Group, 1960
Jahr Quelle:2024
Band/Heft Quelle:73(2024), 9, Seite 1411-1413
ISSN Quelle:1468-3288
Abstract:Liver fibrosis is characterised by the excessive deposition of extracellular matrix (ECM) in response to chronic and sustained liver damage, triggering a prolonged wound healing response. The accumulation of ECM proteins disrupts the normal hepatic architecture, resulting in the development of fibrotic scars and nodules of regenerated hepatocytes, ultimately progressing to cirrhosis. While the acute wound healing response can be transiently initiated, its progression to fibrosis requires chronic exposure to damaging agents, including viral infections, autoimmune disorders, alcohol and drug abuse, cholestatic conditions, and metabolic diseases. - - Cirrhosis represents an advanced stage of liver disease characterised by distorted liver parenchyma, nodule formation, hepatic dysfunction or insufficiency and reduced intrahepatic blood flow leading to portal hypertension.1-3 - - Hepatic stellate cells (HSCs), also termed Ito cells, lipocytes, fat storing or perisinusoidal cells, play a pivotal role in liver fibrosis regardless of its aetiology. They act as major producers of ECM and amplify the fibrogenic response.1 2 In a healthy liver, HSCs reside in the space of Disse in between hepatocytes and liver sinusoidal endothelial cells (LSEC). On liver injury, HSCs undergo activation and differentiation into myofibroblast-like cells, a process that is characterised by proliferation, contraction, inflammation and gain of fibrogenic capabilities. Activated HSCs migrate throughout the liver and thereby accumulate in damaged areas where they are replacing injured …
DOI:doi:10.1136/gutjnl-2023-331785
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: https://doi.org/10.1136/gutjnl-2023-331785
 Volltext: https://gut.bmj.com/content/73/9/1411
 DOI: https://doi.org/10.1136/gutjnl-2023-331785
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:CELL BIOLOGY
 CHRONIC LIVER DISEASE
K10plus-PPN:1899100180
Verknüpfungen:→ Zeitschrift

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