Adipocyte-specific inactivation of acyl-CoA synthetase fatty acid transport protein 4 (Fatp4) in mice causes adipose hypertrophy and alterations in metabolism of complex lipids under high fat diet

Journal of Biological Chemistry

Volumn 286, Issue 41, 2011, Pages 35578-35587

  Lenz, Lena Solveig ^a   Marx, Jana ^a   Chamulitrat, Walee ^a   Kaiser, Iris ^a   Gröne, Hermann Josef ^b   Liebisch, Gerhard ^c   Schmitz, Gerd ^c   Elsing, Christoph ^d   Straub, Beate K ^e   Füllekrug, Joachim ^a   Stremmel, Wolfgang ^a   Herrmann, Thomas ^a,f  

^a UNIVERSITY OF HEIDELBERG   (Germany)

^b GERMAN CANCER RESEARCH CENTER DKFZ   (Germany)

^c UNIVERSITY OF REGENSBURG   (Germany)

^d St Elisabeth Hospital   (Germany)

^e Institute of Pathology   (Germany)

^f Klinikum Idar Oberstein   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ACYL-COA SYNTHETASE; ADIPOCYTES; ADIPOSE TISSUE; BODY WEIGHT; CELLULAR FATTY ACIDS; CHOLESTERYL ESTERS; FAT MASS; FATTY ACID TRANSPORT; HIGH-FAT DIET; HIGHER-DEGREE; IN-VIVO; INSULIN SENSITIVITY; LIPOGENESIS; LONG CHAIN FATTY ACID; MUTANT MICE; SPHINGOMYELIN; STANDARD CONDITIONS; SUBCUTANEOUS FAT;

GENE EXPRESSION; MAMMALS; METABOLISM; MOLECULAR WEIGHT; NUTRITION; PATHOLOGY; PHOSPHOLIPIDS; PHYSIOLOGY; TISSUE;

PALMITIC ACID;

ADIPOCYTOKINE; CHOLESTEROL ESTER; FATTY ACID TRANSPORTER 4; LIGNOCERIC ACID; LONG CHAIN FATTY ACID; PALMITIC ACID; SPHINGOMYELIN;

ADIPOCYTE; ADIPOCYTE HYPERTROPHY; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; FATTY ACID TRANSPORT; FATTY ACID TRANSPORT PROTEIN 4 GENE; FATTY LIVER; GENE; GENE EXPRESSION; GENE INACTIVATION; HYPERTROPHY; IN VIVO STUDY; INSULIN SENSITIVITY; LIPID COMPOSITION; LIPID DIET; LIPOGENESIS; LIVER; METABOLISM; MOUSE; NONHUMAN; OBESITY; PRIORITY JOURNAL; SUBCUTANEOUS FAT; WEIGHT GAIN;

ADIPOCYTES; ADIPOSE TISSUE; ANIMALS; DIETARY FATS; FATTY ACID TRANSPORT PROTEINS; FATTY ACIDS; HYPERTROPHY; LIPID METABOLISM; LIVER; LIVER DISEASES; MICE; MICE, KNOCKOUT;

ANIMALIA; MUS;

EID: 80053901344     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M111.226530     Document Type: Article

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