Endoplasmic reticulum stress impairs cholesterol efflux and synthesis in hepatic cells

Journal of Lipid Research

Volumn 55, Issue 1, 2014, Pages 94-103

  Röhrl, Clemens ^a,b   Eigner, Karin ^a,b   Winter, Katharina ^a,b   Korbelius, Melanie ^c,d   Obrowsky, Sascha ^c,d   Kratky, Dagmar ^c,d   Kovacs, Werner J ^e   Stangl, Herbert ^a,b  

^a MEDICAL UNIVERSITY OF VIENNA   (Austria)

^b Institute of Molecular Biology and Biochemistry   (Austria)

^c MEDICAL UNIVERSITY OF GRAZ   (Austria)

^d Institute of Pharmaceutical Sciences   (Switzerland)

^e ETH ZURICH   (Switzerland)

Author keywords

3 hydroxy 3 methylglutarylcoenzyme A reductase; Apolipoprotein A I; ATP binding cassette transporter A1; HepG2; High density lipoprotein

Indexed keywords

ABC TRANSPORTER A1; APOLIPOPROTEIN A1; HIGH DENSITY LIPOPROTEIN; HIGH DENSITY LIPOPROTEIN CHOLESTEROL; HYDROXYMETHYLGLUTARYL COENZYME A REDUCTASE; LIVER X RECEPTOR; SCAVENGER RECEPTOR B; STEROL REGULATORY ELEMENT BINDING PROTEIN 2;

ACUTE STRESS; ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; BIOGENESIS; CELL COMPARTMENTALIZATION; CELL LEVEL; CELL NUCLEUS; CELL STRAIN HEPG2; CHOLESTEROL METABOLISM; CHOLESTEROL SYNTHESIS; CHOLESTEROL TRANSPORT; CONTROLLED STUDY; ENDOPLASMIC RETICULUM STRESS; ENZYME ACTIVITY; HUMAN; HUMAN CELL; LIPOPROTEIN SYNTHESIS; LIVER CELL; MALE; METABOLIC DISORDER; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN DEFECT; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN LOCALIZATION; RECEPTOR DOWN REGULATION;

3-HYDROXY-3-METHYLGLUTARYL- COENZYME A REDUCTASE; APOLIPOPROTEIN A-I; ATP-BINDING CASSETTE TRANSPORTER A1; HEPG2; HIGH DENSITY LIPOPROTEIN;

ANIMALS; ATP BINDING CASSETTE TRANSPORTER 1; CHOLESTEROL; ENDOPLASMIC RETICULUM STRESS; GENE EXPRESSION; GENE EXPRESSION REGULATION; GLYCOSYLATION; HEP G2 CELLS; HEPATOCYTES; HUMANS; HYDROXYMETHYLGLUTARYL COA REDUCTASES; LIPID METABOLISM; LIVER; MALE; MICE; MICE, INBRED C57BL; ORPHAN NUCLEAR RECEPTORS; PROTEIN PROCESSING, POST-TRANSLATIONAL; STEROL REGULATORY ELEMENT BINDING PROTEIN 2;

EID: 84891370803     PISSN: 00222275     EISSN: 15397262     Source Type: Journal    
DOI: 10.1194/jlr.M043299     Document Type: Article

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