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Intravascular hemolysis triggers NAFLD characterized by a deregulation of lipid metabolism and lipophagy blockade
The Journal of pathology, 2023-10, Vol.261 (2), p.169-183
Rayego‐Mateos, Sandra
Morgado‐Pascual, José Luis
García‐Caballero, Cristina
Lazaro, Iolanda
Sala‐Vila, Aleix
Opazo‐Rios, Lucas
Mas‐Fontao, Sebastian
Egido, Jesús
Ruiz‐Ortega, Marta
Moreno, Juan Antonio
2023
Volltextzugriff (PDF)
Details
Autor(en) / Beteiligte
Rayego‐Mateos, Sandra
Morgado‐Pascual, José Luis
García‐Caballero, Cristina
Lazaro, Iolanda
Sala‐Vila, Aleix
Opazo‐Rios, Lucas
Mas‐Fontao, Sebastian
Egido, Jesús
Ruiz‐Ortega, Marta
Moreno, Juan Antonio
Titel
Intravascular hemolysis triggers NAFLD characterized by a deregulation of lipid metabolism and lipophagy blockade
Ist Teil von
The Journal of pathology, 2023-10, Vol.261 (2), p.169-183
Ort / Verlag
Chichester, UK: John Wiley & Sons, Ltd
Erscheinungsjahr
2023
Quelle
Access via Wiley Online Library
Beschreibungen/Notizen
Intravascular hemolysis is a common feature of different clinical entities, including sickle cell disease and malaria. Chronic hemolytic disorders are associated with hepatic damage; however, it is unknown whether heme disturbs lipid metabolism and promotes liver steatosis, thereby favoring the progression to nonalcoholic fatty liver disease (NAFLD). Using an experimental model of acute intravascular hemolysis, we report here the presence of liver injury in association with microvesicular lipid droplet deposition. Hemolysis promoted serum hyperlipidemia and altered intrahepatic triglyceride fatty acid composition, with increments in oleic, palmitoleic, and palmitic acids. These findings were related to augmented expression of transporters involved in fatty acid uptake (CD36 and MSR1) and deregulation of LDL transport, as demonstrated by decreased levels of LDL receptor and increased PCSK9 expression. Hemolysis also upregulated hepatic enzymes associated with cholesterol biosynthesis (SREBP2, HMGC1, LCAT, SOAT1) and transcription factors regulating lipid metabolism (SREBP1). Increased LC3II/LC3I ratio and p62/SQSTM1 protein levels were reported in mice with intravascular hemolysis and hepatocytes stimulated with heme, indicating a blockade of lipophagy. In cultured hepatocytes, cell pretreatment with the autophagy inductor rapamycin diminished heme‐mediated toxicity and accumulation of lipid droplets. In conclusion, intravascular hemolysis enhances liver damage by exacerbating lipid accumulation and blocking the lipophagy pathway, thereby promoting NAFLD. These new findings have a high translational potential as a novel NAFLD‐promoting mechanism in individuals suffering from severe hemolysis episodes. © 2023 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.
Sprache
Englisch
Identifikatoren
ISSN: 0022-3417
eISSN: 1096-9896
DOI: 10.1002/path.6161
Titel-ID: cdi_proquest_miscellaneous_2848230797
Format
–
Schlagworte
Autophagy
,
CD36 antigen
,
Cholesterol
,
Fatty acid composition
,
Fatty acids
,
Fatty liver
,
Heme
,
Hemolysis
,
Hepatocytes
,
Hyperlipidemia
,
intravascular hemolysis
,
lipid accumulation
,
Lipid metabolism
,
Lipids
,
lipophagy
,
Liver
,
liver damage
,
Liver diseases
,
Low density lipoprotein receptors
,
Metabolism
,
NAFLD
,
Rapamycin
,
Sickle cell disease
,
Steatosis
,
Toxicity
,
Transcription factors
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