Secretion of fatty acid binding protein aP2 from adipocytes through a nonclassical pathway in response to adipocyte lipase activity

Journal of Lipid Research

Volumn 56, Issue 2, 2015, Pages 423-434

  Ertunc, Meric Erikci ^a   Sikkeland, Jørgen ^b   Fenaroli, Federico ^b   Griffiths, Gareth ^b   Daniels, Mathew P ^c   Cao, Haiming ^c   Saatcioglu, Fahri ^b   Hotamisligil, Gökhan S ^a  

^a HARVARD SCHOOL OF PUBLIC HEALTH   (United States)

^b UNIVERSITY OF OSLO   (Norway)

^c NATIONAL HEART LUNG AND BLOOD INSTITUTE   (United States)

Author keywords

Adipokine; Adipose triglyceride lipase; Hormone; Hormone sensitive lipase; Lipolysis; Obesity

Indexed keywords

5 [2 [[2 (3 CHLOROPHENYL) 2 HYDROXYETHYL]AMINO]PROPYL] 1,3 BENZODIOXOLE 2,2 DICARBOXYLIC ACID; ACYLGLYCEROL LIPASE; ADIPOSE TRIGLYCERIDE LIPASE; ATGLISTATIN; BETA 3 ADRENERGIC RECEPTOR; CAY 10499; CYCLIC AMP; CYCLIC AMP DEPENDENT PROTEIN KINASE; DIACYLGLYCEROL; FATTY ACID BINDING PROTEIN 4; FATTY ACID BINDING PROTEIN AP2; ISOPRENALINE; MUTANT PROTEIN; PERILIPIN 1; PROTEIN INHIBITOR; TRIACYLGLYCEROL; TRIACYLGLYCEROL LIPASE; UNCLASSIFIED DRUG; CARRIER PROTEIN; DESNUTRIN PROTEIN, MOUSE; FABP4 PROTEIN, MOUSE; FATTY ACID BINDING PROTEIN; PHOSPHOPROTEIN;

ADIPOCYTE; ADIPOSE TISSUE; ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CELL CULTURE; CONTROLLED STUDY; ENDOSOME; ENZYME ACTIVITY; ENZYME INHIBITION; EX VIVO STUDY; EXOSOME; GENE; GENETIC DISORDER; GLUCOSE METABOLISM; HORMONAL REGULATION; HSL GENE; IN VITRO STUDY; IN VIVO STUDY; LIGAND BINDING; LIPID ANALYSIS; LIPOLYSIS; MALE; NONHUMAN; PROTEIN FUNCTION; PROTEIN LOCALIZATION; PROTEIN SECRETION; PROTEIN TARGETING; SIGNAL TRANSDUCTION; 3T3 CELL LINE; ANIMAL; CONFOCAL MICROSCOPY; FLUORESCENT ANTIBODY TECHNIQUE; GENETICS; KNOCKOUT MOUSE; METABOLISM; MOUSE; SECRETION (PROCESS);

3T3-L1 CELLS; ADIPOCYTES; ADIPOSE TISSUE; ANIMALS; CARRIER PROTEINS; FATTY ACID-BINDING PROTEINS; FLUORESCENT ANTIBODY TECHNIQUE; LIPASE; MALE; MICE; MICE, KNOCKOUT; MICROSCOPY, CONFOCAL; PHOSPHOPROTEINS;

EID: 84921929997     PISSN: 00222275     EISSN: 15397262     Source Type: Journal    
DOI: 10.1194/jlr.M055798     Document Type: Article

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